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I would like to be included in the K-Recruiting applicant pool. This will give me the opportunity to receive further exciting offers. By being included in the applicant pool, K-Recruiting GmbH (DE), K-Recruiting LP (US), K-Recruiting Schweiz AG (CH) and K-Recruiting Global AG (CH) will have access to my personal data and will be able to submit offers to me.

Come to k!

I would like to be included in the K-Recruiting contractor pool. This will give me the opportunity to receive further exciting offers. By being included in the contractor pool, K-Recruiting GmbH (DE), K-Recruiting LP (US), K-Recruiting Schweiz AG (CH) and K-Recruiting Global AG (CH) will have access to my personal data and will be able to submit offers to me.

Are you interested in this project?

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">eLearning &amp; LMS Support Specialist (M/F/D)<o:p></o:p>&nbsp;<o:p></o:p>Tasks:<o:p></o:p><ul style="margin-inline-start: 0px; margin-inline-end: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoListParagraphCxSpFirst" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">2nd level support for our learning management systems Umantis and Ilias<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Run special Umantis reporting, specifically for regular MSBU License Reporting<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Implement new eLearning training in Umantis<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Manage data uploads in Umantis which are essential for assigning mandatory eLearning or optimizing the MSBU license concept as aligned with MSBU management<o:p></o:p></li><li class="MsoListParagraphCxSpLast" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Active ticket handling for Learning Management related problems&nbsp;<o:p></o:p></li></ul><o:p></o:p>&nbsp;Qualification:<o:p></o:p><ul style="margin-inline-start: 0px; margin-inline-end: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoListParagraphCxSpFirst" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Degree in Information Technology, Education, HR, Business Administration, or a related field, or equivalent work experience<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Experience in supporting Learning Management Systems (LMS), preferably Umantis and Ilias<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Experience in eLearning content management and implementation<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Good understanding of LMS administration, including user management, course assignments, and reporting<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Ability to work independently and manage multiple tasks efficiently<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Service-oriented mindset with a proactive approach to ticket handling<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Knowledge of HR systems and their integration with LMS<o:p></o:p></li><li class="MsoListParagraphCxSpLast" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Experience in process optimization for learning management<o:p></o:p></li></ul><o:p></o:p>&nbsp;Requirements:&nbsp;<o:p></o:p>Start: April 1st 2025<o:p></o:p>Duration: 24 months<o:p></o:p>Capacity: 2-3 days per week<o:p></o:p>Location: Hamburg, Germany<o:p></o:p><o:p></o:p>&nbsp;</div>

eLearning & LMS Support Specialist

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">&nbsp;&nbsp;Director of Epidemiology&nbsp;(M/F/D)<o:p></o:p>&nbsp;<o:p></o:p>Tasks:<o:p></o:p><ul style="margin-inline-start: 0px; margin-inline-end: 0px; list-style-type: disc; margin-bottom: 0cm; margin-top: 0cm; padding-inline-start: 40px; width: fit-content;" width="fit-content" type="disc"><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">To design and execute Epidemiology activities and studies adressing safety research questions in the context of drug development, regulatory submissions, and marketed products,<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">To identify epidemiological / pharmaco-epidemiological methods, relevant data sources, best suited to address safety research questions<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">To transfer epidemiologic expertise and deliverables to the evaluation, refinement and contextualization of safety findings and potential signals, evaluation of safety signals (including literature reviews), as well as to the preparation and update of Epidemiology content in safety and regulatory documents (including but not limited to Risk Minimization Plan, FDA/EMA Orphan Drug Designation)<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">To conduct the feasibility, design, preparation of study concepts, protocols, and statistical analysis plans, know-how transfer to analysis execution for the Epi analytical team, and report of pharmacoepidemiologic studies of assigned DS products in line with the strategic epidemiology plan<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">Evaluating the feasibility of establishing multiple indication cohorts for RWE generation using CPRD and other RWD sources<o:p></o:p></li></ul>&nbsp;<o:p></o:p>Qualification:<o:p></o:p><ul style="margin-inline-start: 0px; margin-inline-end: 0px; list-style-type: disc; margin-bottom: 0cm; margin-top: 0cm; padding-inline-start: 40px; width: fit-content;" width="fit-content" type="disc"><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">PhD in Epidemiology and/or pharmacoepidemiology or equivalent advantageous<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">At least 5-year experience in epidemiology/ pharmacoepidemiology as well as in drug safety<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">At least 3-year experience in CRO (pharmacoepidemiology) or pharmaceutical industry<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">Proven experience in executing pharmacoepidemiology studies using RWD, including CPRD<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">Experience in oncology epidemiology preferred<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">Excellent written and oral communication skills in English<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;">Excellent personal and intercultural skills paired with the ability to work cross functionally in a multinational organization<o:p></o:p></li></ul>&nbsp;<o:p></o:p>Requirements:&nbsp;<o:p></o:p>Start: 1.5.25<o:p></o:p>Duration: 15 months<o:p></o:p>Capacity: 5 days per week<o:p></o:p>Location: Greater Munich area; 100% remote possible + travel<o:p></o:p>&nbsp;&nbsp;</div>

Director of Epidemiology

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Director Clinical Operations (M/W/D)&nbsp;Aufgaben:<ul style="background-color: rgb(255, 255, 255); color: rgb(0, 0, 0); font-family: &quot; undefined: TimesNewRoman&quot; font-size: medium; font-style: normal; font-weight: 400; letter-spacing: normal; line-height: 1.5em; margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><li class="text-element-body_text" style="color:rgb(0, 0, 0);font-family:&quot;Open Sans&quot;, sans-serif;font-size:14px;font-weight:400;line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Clinical Trial Oversight &amp; Strategy: Lead and oversee assigned clinical trials, ensuring timely execution within budget and regulatory compliance. Develop clinical trial management strategies, including budget, resourcing, and scenario planning, aligned with the Clinical Development plan. Monitor trial progress, mitigate risks, and implement corrective actions as needed</li><li class="text-element-body_text" style="color:rgb(0, 0, 0);font-family:&quot;Open Sans&quot;, sans-serif;font-size:14px;font-weight:400;line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Leadership &amp; Team Management: Mentor and guide Clinical Trial Managers (CTMs) and Senior CTMs, providing coaching, performance feedback, and career development. Oversee resource allocation to ensure optimal staffing and alignment with study needs. Facilitate communication across teams to ensure alignment on project goals and timelines</li><li class="text-element-body_text" style="color:rgb(0, 0, 0);font-family:&quot;Open Sans&quot;, sans-serif;font-size:14px;font-weight:400;line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Vendor &amp; Budget Oversight: Manage vendor activities (CROs, eCRFs, eTMF, software), ensuring adherence to trial timelines and deliverables. Oversee Work Orders (WOs) and Change Orders in alignment with Master Service Agreements (MSAs), monitor vendor performance, and ensure timely invoice ratification and payments. Review and approve budgets, resource plans, and timelines</li><li class="text-element-body_text" style="color:rgb(0, 0, 0);font-family:&quot;Open Sans&quot;, sans-serif;font-size:14px;font-weight:400;line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Process Improvement &amp; Compliance: Develop and optimize SOPs, workflows, and tools to enhance efficiency and ensure regulatory compliance. Drive continuous improvement initiatives and standardization across clinical operations. Ensure effective use of clinical trial systems (CTMS, eTMF) and collaborate with IT for system optimization</li><li class="text-element-body_text" style="color:rgb(0, 0, 0);font-family:&quot;Open Sans&quot;, sans-serif;font-size:14px;font-weight:400;line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Cross-Functional Collaboration &amp; Reporting: Coordinate with regulatory, data management, and other teams to align on study milestones. Provide updates on trial status, budget, risks, and key accomplishments to leadership. Lead initiatives to enhance collaboration across functions, ensuring operational excellence and strategic alignment</li><li class="text-element-body_text" style="color:rgb(0, 0, 0);font-family:&quot;Open Sans&quot;, sans-serif;font-size:14px;font-weight:400;line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Additional Responsibilities: Oversee training and development of new team members, ensuring smooth onboarding and ongoing learning. Identify process gaps and propose improvements to enhance trial execution. Perform additional tasks as needed to support successful study completion and adherence to Good Clinical Practice (GCP)</li></ul>&nbsp;Qualifikation:<ul class="text-element-body_text" style="background-color: rgb(255, 255, 255); color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-style: normal; font-weight: 400; letter-spacing: normal; line-height: 1.5em; margin-bottom: 14px; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0px; padding-inline-start: 40px; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;"><p class="text-element-body_text" style="color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-weight: 400; line-height: 1.5em; margin: 0px 0 14px;">Graduation from a recognized institution (preferably in Life Sciences, Pharmacy, Chemistry, or Biology) with a focus on clinical research or related fields</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;"><p class="text-element-body_text" style="color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-weight: 400; line-height: 1.5em; margin: 0px 0 14px;">Several years of professional experience in clinical operations, with significant exposure to managing assigned clinical trials. Experience in oncology studies is highly desirable</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;"><p class="text-element-body_text" style="color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-weight: 400; line-height: 1.5em; margin: 0px 0 14px;">Proven experience leading and mentoring Clinical Trial Managers (CTMs) and senior clinical operations teams. Strong interpersonal skills and the ability to manage cross-functional teams effectively</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;"><p class="text-element-body_text" style="color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-weight: 400; line-height: 1.5em; margin: 0px 0 14px;">In-depth understanding of assigned clinical trial processes, from protocol development to trial completion. Expertise in clinical trial design, risk management, and vendor oversight</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;"><p class="text-element-body_text" style="color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-weight: 400; line-height: 1.5em; margin: 0px 0 14px;">Comprehensive knowledge of FDA, EMA, ICH/GCP regulations and guidelines. Familiarity with global regulatory requirements for clinical trials</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;"><p class="text-element-body_text" style="color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-weight: 400; line-height: 1.5em; margin: 0px 0 14px;">Experience in using clinical trial management systems (CTMS, eTMF) and implementing SOPs and templates to standardize and optimize trial processes</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;"><p class="text-element-body_text" style="color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-weight: 400; line-height: 1.5em; margin: 0px 0 14px;">Strong ability to analyse trial data, identify risks, and implement corrective actions to ensure trials stay on track</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;"><p class="text-element-body_text" style="color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-weight: 400; line-height: 1.5em; margin: 0px 0 14px;">Excellent written and verbal communication skills in English (additional languages are a plus). Ability to clearly articulate trial progress, challenges, and strategies to senior leadership</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;"><p class="text-element-body_text" style="color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-weight: 400; line-height: 1.5em; margin: 0px 0 14px;">Strong problem-solving skills with a proactive, goal-oriented approach to addressing challenges. Ability to make decisions under pressure while maintaining trial integrity</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;"><p class="text-element-body_text" style="color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-weight: 400; line-height: 1.5em; margin: 0px 0 14px;">Oncology Experience: Solid background in oncology, with a deep understanding of current therapies and emerging trends in the field. Interest in innovative therapies and clinical trial designs is a plus</li></ul>&nbsp;Rahmendaten:&nbsp;Start: asapDauer: FestanstellungAuslastung: 5 Tage die WocheEinsatzort: München &amp; Remote&nbsp;&nbsp;&nbsp;</div>

Director Clinical Operations (m/w/d)

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Global Medical Safety Scientist (M/W/D)&nbsp;Aufgaben:<ul class="text-element-body_text" style="margin-inline-start: 0px; margin-inline-end: 0px; background-color: rgb(255, 255, 255); color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-style: normal; font-weight: 400; letter-spacing: normal; line-height: 1.5em; margin-bottom: 14px; margin-top: 0px; padding-inline-start: 40px; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">ICSR preliminary assessment and medical review in Argus Safety</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Contribute to medical safety relevant sections in Aggregate safety reports and Risk Management Plans</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Elaborate and maintain list of safety concerns</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Perform signal detection and safety signal assessment</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Act as safety matter expert in the development and maintenance of product information</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Evaluate, review, and approve assessments of safety findings from literature</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Prepare responses to safety inquiries received from internal or external stakeholders</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Collaborate for the preparation of safety materials for internal and external safety and labelling boards</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Manage and assess SAE reconciliation discrepancies and provide medical safety input for their resolution</li></ul>&nbsp;Qualifikation:<ul class="text-element-body_text" style="margin-inline-start: 0px; margin-inline-end: 0px; background-color: rgb(255, 255, 255); color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-style: normal; font-weight: 400; letter-spacing: normal; line-height: 1.5em; margin-bottom: 14px; margin-top: 0px; padding-inline-start: 40px; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Degree as Medical Doctor; previous clinical experience is a plus</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Solid organizational skills and experience working cross-functionally and trans-nationally</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Multiple years of experience in a similar role in the pharmaceutical industry or CRO; Oncology experience preferred</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Experience to work in safety databases, ideally Argus Safety</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Solid project and time management skills</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Demonstrated leadership skills, with a proactive, strategic mindset</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Excellent interpersonal skills and the ability to communicate with internal and external subject matter experts both</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Fluent written and spoken English</li></ul>&nbsp;Rahmendaten:&nbsp;Start: asapDauer: FestanstellungAuslastung: 5 Tage die WocheEinsatzort: München &amp; Remote&nbsp;</div>

Global Medical Safety Scientist

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Freelancer - HR Data Entry Specialist (M/W/D)<o:p></o:p>&nbsp;<o:p></o:p>Aufgaben:&nbsp;<o:p></o:p><ul style="padding-inline-start: 40px; margin-inline-start: 0px; margin-inline-end: 0px; width: fit-content;" width="fit-content"><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Beratung bei HR-Prozessen – Thema: Zeiterfassung<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Erfassung von Krankmeldungen sowie Verarbeitung der elektronischen Arbeitsunfähigkeitsbescheinigung (eAU), inklusive Rückmeldungen der Krankenkassen<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Überwachung des Endes der Lohnfortzahlung (LFZ), Prüfung von Vorerkrankungen und Übermittlung der elektronischen Bescheinigung für das Krankengeld<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Verarbeitung von EEL-Rückmeldungen der Krankenkassen<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Korrektur von Stempelzeiten in der Zeiterfassung (manuelle Nachbearbeitung je nach Schichtmodell), Überwachung von Schichtzuschlägen und Verrechnung von Überstunden<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Prüfung der Übertragungen von Dormakaba ins SAP<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Monatliche Kontrolle und Korrektur der Zeiterfassungsdaten<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Anpassung von Arbeitszeitplänen im HR-System bei Bedarf<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Erfassung von Kind-Krank-Meldungen und Einleitung der Folgeprozesse inklusive elektronischer Bescheinigung für das Krankengeld<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Prüfung von Zeitanträgen in Dormakaba (z. B. Sonderurlaub, Freischicht)<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Beratung bei der Bearbeitung von Zeiteinträgen in Dormakaba<o:p></o:p></li></ul>&nbsp;<o:p></o:p>Qualifikation:<o:p></o:p><ul style="padding-inline-start: 40px; margin-inline-start: 0px; margin-inline-end: 0px; width: fit-content;" width="fit-content"><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">HR Erfahrung, idealerweise im Bereich Zeiterfassung und Krankmeldungen<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">SAP HCM Kenntnisse und bestenfalls Dormakaba (oder vergleichbaren Zeiterfassungssystemen)<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Kenntnisse in den gesetzlichen Vorgaben zur Lohnfortzahlung, Krankengeld und EEL-Verfahren<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Selbstständige und strukturierte Arbeitsweise<o:p></o:p></li><li class="MsoListParagraph" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;">Must-Have: Deutsch<o:p></o:p></li></ul>&nbsp;Rahmendaten:<o:p></o:p>Start:&nbsp;Ab sofort, Spätestens April 2025<o:p></o:p>Dauer:&nbsp;6 Monate<o:p></o:p>Auslastung:&nbsp;4-5 Tage pro Woche<o:p></o:p>Einsatzort:&nbsp;Vor Ort – Südliches Baden-Württemberg</div>

Freelancer - HR Data Entry Specialist

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Sr. HR Project Manager - Facility Management Outsourcing (M/F/D): <o:p></o:p>Tasks:<o:p></o:p><ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px; width: fit-content;" type="disc" width="fit-content"><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;tab-stops:list 36.0pt;">Oversee HR coordination for the outsourcing of facility management services across multiple regions.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;tab-stops:list 36.0pt;">Develop HR transfer strategies while ensuring full compliance with TUPE regulations.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;tab-stops:list 36.0pt;">Collaborate with legal experts and advise local HR teams on employment law requirements.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;tab-stops:list 36.0pt;">Gather and analyze employee data to support transition planning.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;tab-stops:list 36.0pt;">Create and implement communication strategies and stakeholder engagement materials.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;tab-stops:list 36.0pt;">Engage with works councils and unions at a central level.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;tab-stops:list 36.0pt;">Supervise and manage the creation and approval process of LTAs.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;tab-stops:list 36.0pt;">Organize training programs and ensure adherence to legal and procedural requirements.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;tab-stops:list 36.0pt;">Act as the main point of contact for local HR teams and senior leadership.<o:p></o:p></li></ul>Qualifications:<o:p></o:p><ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px; width: fit-content;" type="disc" width="fit-content"><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l2 level1 lfo2;tab-stops:list 36.0pt;">Demonstrated experience in (HR) project management, preferably within outsourcing or facility management.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l2 level1 lfo2;tab-stops:list 36.0pt;">Strong knowledge of employment law, TUPE regulations, and HR transition processes.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l2 level1 lfo2;tab-stops:list 36.0pt;">Proven ability to manage stakeholders effectively, including collaboration with unions and works councils.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l2 level1 lfo2;tab-stops:list 36.0pt;">Excellent communication skills, with a background in developing and executing communication strategies.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l2 level1 lfo2;tab-stops:list 36.0pt;">Proficiency in data analysis, risk evaluation, and document management.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l2 level1 lfo2;tab-stops:list 36.0pt;">Experience in leading cross-functional teams and handling complex, multi-country projects.<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l2 level1 lfo2;tab-stops:list 36.0pt;">Fluency in English, with strong written and verbal communication abilities.<o:p></o:p></li></ul>Requirements:<o:p></o:p><ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px; width: fit-content;" type="disc" width="fit-content"><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo3;tab-stops:list 36.0pt;">Start: 1.4.25<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo3;tab-stops:list 36.0pt;">Duration: 12 months<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo3;tab-stops:list 36.0pt;">Capacity: Fulltime<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo3;tab-stops:list 36.0pt;">Location: Remote<o:p></o:p></li></ul>&nbsp;</div>

Sr. HR Project Manager - Facility Management Outsourcing

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Technischer Dokumentationsspezialist (M/W/D)&nbsp;&nbsp;<o:p></o:p>&nbsp;<o:p></o:p>&nbsp;<o:p></o:p>Aufgaben:<o:p></o:p><ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px; width: fit-content;" type="disc" width="fit-content"><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;">Erstellung aller für die Auftragsabwicklung erforderlichen technischen Dokumentationen (Betriebsanleitungen mit Cosima-Go) nach Maschinenrichtlinie 2006/42/eg für Sondergeräte und Maschinen aus dem Sondermaschinenbau<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;">Durchführung und Anpassung von Risikoanalysen sowie deren Überprüfung und Aktualisierung<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;">Überprüfung und Aktualisierung bestehender Dokumentations-Templates, um sicherzustellen, dass alle Informationen aktuell und korrekt sind<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;">Mitwirkung bei der Standardisierung von Templates für technische Doku/ Manuals mit Augenmerk auf die Einhaltung von Produktsicherheit und -konformität gemäß CE, RoHS, REACH<o:p></o:p></li></ul>&nbsp;<o:p></o:p>Qualifikation:<o:p></o:p><ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px; width: fit-content;" type="disc" width="fit-content"><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo2;tab-stops:list 36.0pt;">Maschinebauhintergrund<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo2;tab-stops:list 36.0pt;">Erfahrung mit Component Management Systemen<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo2;tab-stops:list 36.0pt;">Knowledge der Richtlinien: CE, RoHS, REACH<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo2;tab-stops:list 36.0pt;">Sprachkenntnisse: Englisch und Deutsch<o:p></o:p></li></ul>&nbsp;<o:p></o:p>Rahmendaten:&nbsp;<o:p></o:p>Start: asap<o:p></o:p>Dauer: 6 Monate<o:p></o:p>Auslastung: 5 Tage die Woche<o:p></o:p>Einsatzort: Remote (80%) und Großraum Kassel<o:p></o:p></div>

Technischer Dokumentationsspezialist

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Category Manager (M/F/D)<o:p></o:p>&nbsp;<o:p></o:p>Tasks:<o:p></o:p><ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px; width: fit-content;" type="disc" width="fit-content"><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;tab-stops:list 36.0pt;">Clarify/ negotiate to incoterms and logistics conditions with various suppliers, thereafter, update the system and communicate to the relevant stakeholders<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;tab-stops:list 36.0pt;">Work with suppliers to ensure timely PO and delivery confirmations to avoid supply chain disruption and escalation<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;tab-stops:list 36.0pt;">Analyze cost trends, develop cost breakdown, and review forecasts and translate them into implications for the business and Category management<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;tab-stops:list 36.0pt;">Prepare relevant benchmark data, supply market intelligence info in preparation to supplier negotiations<o:p></o:p></li><li class="MsoNormal" style="line-height:115%;margin-bottom:8pt;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;tab-stops:list 36.0pt;">Scout for new suppliers and develop the supply base according to the category strategy<o:p></o:p></li></ul>&nbsp;<o:p></o:p>Requirements:&nbsp;<o:p></o:p>Start: 15.03.2025<o:p></o:p>Duration: 3 months<o:p></o:p>Capacity: 5 days per week<o:p></o:p>Location: Großraum Kassel + max. 1 T/Wo remote<o:p></o:p></div>

Category Manager

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;"><a name="_Hlk51924843">Medical Advisor Dermatology (M/W/D)&nbsp;</a>&nbsp;<o:p></o:p>&nbsp;&nbsp;<o:p></o:p>Aufgaben:&nbsp;<o:p></o:p><ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Bereitstellung medizinischer Expertise im dermatologischen Bereich&nbsp;</li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Life-Cycle-Management&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Medizinisch-wissenschaftliche Prüfung von Werbematerialien (Flyer, Broschüren, Websites, Social Media, etc.)&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Sicherstellen, dass alle Inhalte den regulatorischen Vorgaben (z. B. EFPIA, FSA, AMG) entsprechen&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Zusammenarbeit mit Marketing-, Compliance- und Rechtsabteilungen zur finalen Freigabe&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Nutzung von PromoMats oder ähnlichen Systemen zur Freigabe und Dokumentation&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Auswahl relevanter nationaler und internationaler Kongresse für Unternehmenspräsenz&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Planung und Organisation von Satellitensymposien, Roundtables und Workshops&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Identifikation und Management von Key Opinion Leaders (KOLs)&nbsp;&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Erstellung von wissenschaftlichen Präsentationen, Poster und Vortragsmaterialien&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Input zur Medical Affairs Strategie&nbsp;&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l1 level1 lfo1;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Zusammenarbeit mit internen Teams (Marketing, Vertrieb, Market Access), um wissenschaftlich fundierte Strategien zu entwickeln<o:p></o:p></li></ul>&nbsp;&nbsp;<o:p></o:p>&nbsp;&nbsp;<o:p></o:p>Qualifikation:&nbsp;<o:p></o:p><ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo2;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Abgeschlossenes naturwissenschaftliches oder medizinisches Studium (z. B. Medizin, Pharmazie, Biologie, Biochemie)&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo2;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Mehrjährige Erfahrung als Medical Advisor oder in einer vergleichbaren medizinisch-wissenschaftlichen Rolle<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo2;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Expertise im Bereich Dermatologie und / oder Immunologie&nbsp;&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo2;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Sicheres Auftreten und Kommunikationsgeschick im wissenschaftlichen Umfeld&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo2;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Fähigkeit, komplexe medizinische Inhalte verständlich zu vermitteln&nbsp;&nbsp;<o:p></o:p></li><li class="MsoNormal" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo2;mso-margin-bottom-alt:auto;mso-margin-top-alt:auto;tab-stops:list 36.0pt;">Sehr gute Deutsch- und Englischkenntnisse<o:p></o:p></li></ul>&nbsp;&nbsp;<o:p></o:p>&nbsp;&nbsp;<o:p></o:p>Rahmendaten:&nbsp;&nbsp;<o:p></o:p>Start: asap&nbsp;&nbsp;<o:p></o:p>Dauer: 3 - 6 Monate&nbsp;<o:p></o:p>Auslastung: 20 Stunden / Woche&nbsp;&nbsp;<o:p></o:p>Einsatzort: remote&nbsp;&amp; vereinzelt Kongressbesuche&nbsp;&nbsp;<o:p></o:p></div>

Medical Advisor Dermatology

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">QC Analyst (M/F/D)&nbsp;Tasks:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px; width: fit-content;" type="disc" width="fit-content"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">You are the entry point for the QC laboratories, your main role is to provide the laboratories with all the samples, stabilities and articles necessary for the analyses.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Control, aliquot, identify, record, distribute, store or destroy samples, in accordance with the operational procedures in force and in compliance with Good Manufacturing Practices.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Respect the good reception, processing and distribution practices defined in the procedures/protocols.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Record, document and communicate to the relevant departments any deviation observed upon receipt of samples.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Receive and complete the attributes specific to each sample in the appropriate system (if applicable) according to the defined deadlines.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Receive and record backup samples in the appropriate system.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Record backup sample transfers in the appropriate listed equipment.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Perform backup outputs according to requests made by laboratories via the appropriate system.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Perform Backup sample destruction via the appropriate system.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Send samples to external sites or regulatory authorities according to defined schedules and procedures in force.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Prepare cryotubes for sampling for production areas when applicable.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Participate in the execution of validation protocols and stability studies for which you are responsible for the samples from their reception to their availability for analysis, or to their stabilization and destruction when applicable.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Participate in the management of the stock of consumables and reagents used in laboratories by ensuring orders and replenishment of items within the defined deadlines.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Ensure regular maintenance, calibration of the equipment used, check temperature alarms according to current procedures as well as the correct completion of log-books and their review.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Support QC teams in tasks not related to testing (preparation of solutions for analysis, freezer transfer, autoclaving activity, etc.)</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Each employee is required to respect and apply EHS rules. If he notices deviations from these rules on the part of colleagues or external stakeholders, he also plays an active role in reminding the people concerned of the application of EHS rules<span style="background-color:rgb(255,255,255);color:rgb(29,45,62);font-family:&quot;72&quot;, -apple-system, BlinkMacSystemFont, &quot;Segoe UI&quot;, Roboto, &quot;Helvetica Neue&quot;, Arial, sans-serif, &quot;Apple Color Emoji&quot;, &quot;Segoe UI Emoji&quot;, &quot;Segoe UI Symbol&quot;;font-size:14px;"><span style="display:inline !important;float:none;font-style:normal;font-weight:400;letter-spacing:normal;text-align:left;text-indent:0px;text-transform:none;white-space:normal;width:fit-content;word-spacing:0px;" width="fit-content">.</li></ul>&nbsp;Requirements:&nbsp;Start: 17.03.2025Duration: 6 monthsCapacity: 5 days per weekLocation: Neuchatel Area, Switzerland</div>

QC Analyst

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Sales Representative (M/F/D)&nbsp;Tasks:<ul style="padding-inline-start: 40px; margin-inline-start: 0px; margin-inline-end: 0px;"><li style="width:fit-content;" data-end="111" data-start="29" width="fit-content">Selling the wide range of products in hospitals, nursing homes, and pharmacies</li><li style="width:fit-content;" data-end="175" data-start="112" width="fit-content">Exploring and developing the market in the Canton of Ticino</li><li style="width:fit-content;" data-end="237" data-start="176" width="fit-content">Strengthening sales channels and communication strategies</li><li style="width:fit-content;" data-end="304" data-start="238" width="fit-content">Conducting market analysis and achieving defined sales targets</li><li style="width:fit-content;" data-end="378" data-start="305" width="fit-content">Consolidating and expanding the network of Key Opinion Leaders (KOLs)</li><li style="width:fit-content;" data-end="452" data-start="379" width="fit-content">Actively participating in regional and national events and congresses</li><li style="width:fit-content;" data-end="513" data-start="453" width="fit-content">Implementing sales and marketing strategies in the field</li></ul>&nbsp;Qualification:<ul style="padding-inline-start: 40px; margin-inline-start: 0px; margin-inline-end: 0px;"><li style="width:fit-content;" data-end="849" data-start="737" width="fit-content">Solid experience in sales of pharmaceutical products, clinical nutrition, and medical devices in Switzerland</li><li style="width:fit-content;" data-end="938" data-start="850" width="fit-content">In-depth knowledge of the hospital and healthcare environment in the relevant region</li><li style="width:fit-content;" data-end="1030" data-start="939" width="fit-content">Strong customer orientation and teamwork skills, with excellent communication abilities</li><li style="width:fit-content;" data-end="1127" data-start="1031" width="fit-content">High willingness to achieve top performance, flexibility, and ability to work under pressure</li><li style="width:fit-content;" data-end="1221" data-start="1128" width="fit-content">Native Italian speaker with the ability to communicate well in German, English, or French</li><li style="width:fit-content;" data-end="1278" data-start="1222" width="fit-content">Category B driving license and willingness to travel</li></ul>&nbsp;Requirements:&nbsp;Start: 01.04.2025Capacity: 90-100%Location: Ticino&nbsp;</div>

Sales Representative

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Clinical Supplies Quality Specialist (M/F/D)&nbsp;Tasks:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Responsible from release of clinical and commercial drugs for packaging, incoming label stock and primary packaging components to release of clinical finished goods</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Review and release of incoming label stock</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Review, and release of clinical finished goods, including review of the printed and applied label</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">GMP review of the batch record and review of the regulatory fillings and the final release&nbsp;</li></ul>&nbsp;Qualification:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Previous experience in a similar role is highly appreciated, university degree (bachelor or higher) is preferred, experience in a regulated environment is an advantage</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Minimum of 2 years in a regulated environment (pharma, medtech preferred)</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">English C1 mandatory, German is nice to have</li></ul>&nbsp;Requirements:&nbsp;Start: 01.04.2025Duration: 6 monthsCapacity: 5 days per weekLocation: Werthenstein, Switzerland&nbsp;</div>

Clinical Supplies Quality Specialist

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">QA Associate (M/F/D)&nbsp;Tasks:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="xmsonormal" style="margin-right:0cm;">Handling of shopfloor oversight over the manufacturing operations, eBR and elogbook review (LIMS and samples, QRMs…)&nbsp;(60%)</li><li class="xmsonormal" style="margin-right:0cm;">Executes QA activities related to downstream operations, GMP manufacturing,&nbsp; and downstream equipment to ensure the safety, efficacy and purity of the products manufactured&nbsp;<o:p></o:p></li><li class="xmsonormal" style="margin-right:0cm;">Reviews and approves GMP Engineering and Manufacturing documents during both project and operational phases of the site, specifically related to procedures, work instructions, CAPAs, deviations, change control, equipment (work orders, P&amp;IDs, qualification protocols,&nbsp;calibration deviations..,) etc.<o:p></o:p></li><li class="xmsonormal" style="margin-right:0cm;">Partners with Manufacturing, Manufacturing Sciences, Process Engineering, Automation SMEs during deviation management and investigations.<o:p></o:p></li><li class="xmsonormal" style="margin-right:0cm;">Take part to the monitoring and release activities for Column Packing / Unpacking and Chromatography Review.<o:p></o:p></li><li class="xmsonormal" style="margin-right:0cm;">Ensures adherence to internal procedures during downstream manufacturing operations or for equipment controls and release before and during GMP CAPEX and OPEX project (i.e., shutdowns, construction projects) or New product introduction<o:p></o:p></li><li class="xmsonormal" style="margin-right:0cm;">Take part of the Quality On-Call duty rotation for Quality&nbsp;<o:p></o:p></li><li class="xmsonormal" style="margin-right:0cm;">Participates in batch record review and close out in the view of batch release.<o:p></o:p></li></ul>&nbsp;Qualification:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li>Bachelor’s degree in relevant field such as Chemical Engineering, Bioengineering, Biotechnology, Bioprocessing, Pharmaceutical Sciences, Pharmaceutical Regulations and at least 6 years&nbsp;of experience in pharmaceutical or biotech manufacturing environment.&nbsp;<o:p></o:p></li><li>&nbsp;Master’s degree in relevant field such as Chemical Engineering, Bioengineering, Biotechnology, Bioprocessing, Pharmaceutical Sciences, Pharmaceutical Regulations and at least 4 years of experience in pharmaceutical or biotech manufacturing environment.</li><li>&nbsp;Experience with Quality Assurance, Equipment Qualification, Downstream Process is preferred</li><li>Demonstrated ability to work autonomously with cross-functional team members.</li><li>English B1 as a minimum.</li></ul>&nbsp;Requirements:&nbsp;Start: 01.04.2025Duration: 7 monthsCapacity: 5 days per weekLocation: Greater Solothurn Area</div>

QA Associate

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Sr Material Planning Analyst (M/F/D)&nbsp;Tasks:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">The employee will be responsible for Coordinating and supporting the execution of activities in the Warehouse within Solothurn as per procedures and policies.&nbsp;</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Responsible for raw materials planning and inventory control activities, including forecasted demand, safety stock levels, expiry reporting, TD forecasting, QC release, and the weekly management of ASCP purchasing suggestions. 25%</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Revises and maintains SOPs, SLRs, BOM’s, Formulas, Recipes, Validity Rules, Production Rules, Warehouse Rules in OPM. 25%</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Supports new item creation process and Master Data enrichment as required. 10%</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Responsible for reviewing process and raw material vendor change notifications for inventory impact and facilitation of cross-functions discussions, as required, to drive changes to closure and/or visibility of change or inventory impact. 10%</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Supports tech transfers and the development/maintenance of manufacturing bills of materials, as needed, and ensures that the raw materials are procured and on-hand to support the manufacturing schedule. 15%</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Analyzes data and creates the Expired and Obsolete report quarterly and reviews the information with the site planning management team. 5%</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Supports site leadership team meetings as needed and escalates potential issues to management as required. 5%</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">And Other job duties that may assigned at any time per business needs</li></ul>&nbsp;Qualification:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Minimum educational level necessary to perform the job (High School diploma, Associate’s Degree, Bachelor’s Degree, Masters, PhD)&nbsp;</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">3-5 years of relevant supply chain experience and/or training in a GMP regulated industry or an equivalent combination of education and experience.</li><li class="MsoListParagraphCxSpFirst" style="line-height:115%;margin-bottom:10.0pt;margin-right:0cm;margin-top:0cm;">Ability to interact with a cross functional team effectively within organization<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:10.0pt;margin-right:0cm;margin-top:0cm;">Highly detailed oriented with excellent documentation skills&nbsp;<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:10.0pt;margin-right:0cm;margin-top:0cm;">Solid knowledge of business and planning in a GMP manufacturing facility;&nbsp;</li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:10.0pt;margin-right:0cm;margin-top:0cm;">Solid knowledge of Manufacturing Systems (Oracle or other ERP Systems like SAP)</li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:10.0pt;margin-right:0cm;margin-top:0cm;">Solid understanding of the basic QA and cGMP principles<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:10.0pt;margin-right:0cm;margin-top:0cm;">Identifies system constraints and enhancements and leads/supports capitol project and continuous improvement initiatives&nbsp;<o:p></o:p></li><li class="MsoListParagraphCxSpLast" style="line-height:115%;margin-bottom:10.0pt;margin-right:0cm;margin-top:0cm;">Fundamental level of technical writing skills, Intermediate to advanced skills in Microsoft Office<o:p></o:p> &nbsp;</li></ul>&nbsp;Requirements:&nbsp;Start: asapDuration: 12 monthsCapacity: 5 days per weekLocation: Greater Solothurn Area&nbsp;</div>

Sr Material Planning Analyst

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Qualifizierungs-/ Validierungsexperte &nbsp;(M/W/D)&nbsp;Aufgaben:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" data-end="614" data-start="17" width="fit-content"><li data-end="126" data-start="17">Qualifizierung von Produktions- und Prüfanlagen sowie Validierung der Prozesse in der Medizintechnikmontage</li><li data-end="250" data-start="127">Planung und Durchführung von Qualifizierungs- und Validierungsaktivitäten für computergestützte Systeme in der Produktion</li><li data-end="325" data-start="251">Revalidierung und projektbezogene Qualifizierungs-/Validierungsmaßnahmen</li><li data-is-only-node data-end="413" data-start="326">Bearbeitung von Abweichungen während der Qualifizierung/Validierung bis zum Abschluss</li><li data-end="459" data-start="414">Erstellung und Moderation von Prozess-FMEAs</li><li data-end="526" data-start="460">Anfertigung von Testplänen und Reports (FAT/SAT, DQ, IQ, OQ, PQ)</li><li data-end="614" data-start="527">Mitwirkung bei der Weiterentwicklung und Effizienzsteigerung der Validierungsprozesse</li></ul>&nbsp;Qualifikation:<div style="--ck-color-selector-caption-background:hsl(0, 0%, 97%);--ck-color-selector-caption-text:hsl(0, 0%, 20%);--ck-image-style-spacing:1.5em;--ck-inline-image-style-spacing:calc(var(--ck-image-style-spacing) / 2);font-family:Segoe UI;font-size:11pt;"><ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content" data-start="633" data-end="1186" data-is-only-node data-is-last-node><li data-start="633" data-end="761">Erfahrung in der Prozess- und Methodenvalidierung im Bereich Medizintechnik, mit selbstständiger Arbeit nach GMP-Anforderungen</li><li data-start="762" data-end="822">Idealerweise Erfahrung in Software-Validierung (GAMP, GMP)</li><li data-start="823" data-end="914">Fundierte Kenntnisse in der FMEA-Methodik und Erfahrung mit FMEA-Software (z. B. APIS IQ)</li><li data-start="915" data-end="966" data-is-only-node>Gute Statistikkenntnisse (Six Sigma, ISO 22514-7)</li><li data-start="967" data-end="1008">Systematische, analytische Arbeitsweise</li><li data-start="1009" data-end="1056">Eigeninitiative und Verantwortungsbewusstsein</li><li data-start="1057" data-end="1108">Teamfähigkeit, Flexibilität und soziale Kompetenz</li><li data-start="1109" data-end="1140">Sicherer Umgang mit MS-Office</li><li data-start="1141" data-end="1186" data-is-last-node>Gute Englischkenntnisse in Wort und Schrift</li></ul></div>&nbsp;Rahmendaten:&nbsp;Start: Ab sofort; spätestens 14.04.25Dauer: 6 MonateAuslastung: 5 Tage die WocheEinsatzort: BaWü/Remote 3/2&nbsp;</div>

Qualifizierungs-/ Validierungsexperte

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Interim Product Manager Urology (M/W/D)&nbsp;Aufgaben:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li>Aufbau und Weitergabe eines fundierten Marktverständnisses für das entsprechende Portfolio</li><li>Erstellung und Anpassung lokaler Marketing- und Vertriebsstrategien basierend auf dem globalen Brand Plan</li><li>Durchführung der Marketing-Business-Pläne</li><li>Regelmäßige Überprüfung und Anpassung der Marketingmaßnahmen in Bezug auf die Verkaufs- und Umsatzziele</li><li>Entwicklung einer effektiven Strategie für die Kundenbetreuung</li><li>Optimierung des Portfolios und Management des gesamten Lebenszyklus der Produkte&nbsp;</li></ul>&nbsp;Qualifikation:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Einschlägiger Background in der Urologie&nbsp;</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Wünschenswert: Erfahrung in der Onkologie</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Ausgeprägtes Verständnis des deutschen marktes</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Gute Erfahrungen im ambulanten oder Kliniken-Bereich</li></ul>&nbsp;Rahmendaten:&nbsp;Start: ASAP / Spätestens 01.04.2025Dauer: 6 MonateAuslastung: 5 Tage die WocheEinsatzort: Norddeutschland&nbsp;&nbsp;</div>

Interim Product Manager Urology

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Aggregate Report PV Scientist (M/F/D)&nbsp;The Aggregate Reports PV Scientist is part of the Safety Surveillance and Aggregate (SSA) Reports team and is responsible for managing the processes for all aggregate reports (PSURs, DSURs, PADERs and local reports).<o:p></o:p>&nbsp;Tasks:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Project management and authoring of aggregate safety reports such as PSURs, DSURs, PADERs, local reports in collaboration with the PV scientist Lead.<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Serves as a subject matter expert on relevant safety requirements, company policies/procedures related to pharmacovigilance activities, as well as aggregate reports knowledge.&nbsp;<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Support with process improvement; implements and maintains processes.&nbsp;&nbsp;<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Responsible for the Aggregate Reports Master Schedule and worldwide legislation overview (production, update, stakeholders review).<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">In collaboration with PV Scientist lead coordinates and authors responses to safety questions from regulatory authorities.</li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Contributes to initiatives for process improvement and consistency regarding aggregate reporting, clinical trial safety oversight, signal management and responding to ad hoc safety questions.</li></ul>&nbsp;Qualification:<div style="--ck-color-selector-caption-background:hsl(0, 0%, 97%);--ck-color-selector-caption-text:hsl(0, 0%, 20%);--ck-image-style-spacing:1.5em;--ck-inline-image-style-spacing:calc(var(--ck-image-style-spacing) / 2);font-family:Segoe UI;font-size:11pt;"><div style="direction:ltr;margin-left:0in;margin-top:0in;width:6.5in;"><div style="direction:ltr;margin-left:0in;margin-top:0in;width:6.5in;"><ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li>Bachelor’s Degree in biologic or natural science Advanced degree (MSc, PhD, MPH, PharmD, etc.)</li><li>Minimum 8- 10 years Pharmacovigilance experience, including experience in aggregate safety reports writing and safety signal management. Minimum of 2 years managing direct reports</li></ul></div></div></div><ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Understands, interprets, analyzes, and clearly presents scientific and medical data in verbal and written format (including intermediate understanding and application of medical concepts and terminology).&nbsp;<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Interacts collaboratively and effectively in a team environment (including Safety, Clinical Development, Medical Affairs, Clinical Operations, and Regulatory), as well as with external colleagues&nbsp;<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Management and authoring of aggregate data reports.<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Represents and speaks to processes in cross-Safety and cross-functional forums.<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Familiarity with Pharmacovigilance and drug development, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations. Includes familiarity with case processing, expedited reporting rules, and safety database concepts<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Strong organizational skills, including the ability to prioritize independently with minimal supervision.&nbsp;</li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:6.0pt;">Basic knowledge of common data processing software (EXCEL, PowerPoint, Microsoft Word, Business Objects). Knowledge of common safety database systems.</li></ul>&nbsp;Requirements:&nbsp;Start: asapDuration: 12 monthsCapacity: 5 days per weekLocation: Greater Baar Area&nbsp;</div>

Aggregate Report PV Scientist

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Brand Manager (M/W/D)&nbsp;Aufgaben:<ul style="list-style-type: disc; margin-bottom: 0in; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0in; padding-inline-start: 40px; unicode-bidi: embed; width: fit-content;" type="disc" width="fit-content"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Konzeption und Umsetzung innovativer Marketingmaßnahmen für verschiedene Zielgruppen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Entwicklung, Beratung und Implementierung von Mediaplänen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Beratung bei der Entwicklung von zielgruppenspezifischen Messaging</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Crossfunktionale Zusammenarbeit</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Projekt Management</li></ul>&nbsp;Qualifikation:<ul style="list-style-type: disc; margin-bottom: 0in; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0in; padding-inline-start: 40px; unicode-bidi: embed; width: fit-content;" type="disc" width="fit-content"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Abgeschlossenes betriebswirtschaftliches, naturwissenschaftliches oder vergleichbares Studium</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Erfahrung im Bereich Produkt &amp; Brand Management</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Projekt Management Erfahrung</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Must have: Erfahrung im Bereich Rare Diseases</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Must have: Deutsch &amp; Englisch in Wort &amp; Schrift</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Erfahrung mit Veeva, Freigabeprozesse&nbsp;</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Agiles Mindset</li></ul>&nbsp;Rahmendaten:&nbsp;Start: asap, spätestens 01.05.25Dauer: 6 Monate+Auslastung: 5 Tage die WocheEinsatzort: Remote + gelgentlich vor Ort in Bayern&nbsp;</div>

Brand Manager

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Brand Manager (M/W/D)&nbsp;Aufgaben:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Entwicklung der Markenstrategie und Leitung, Identifikation wichtiger taktischer Initiativen und Materialien von der Gestaltung bis zur Umsetzung – Sicherstellung, dass die Teams vor Ort diese anpassen, ausführen und konsistent und effektiv umsetzen (z. B. Markenwerbematerialien, Botschaften und Ansprüche, Medienmaterialien, effektive Kanalauswahl entsprechend Omnichannel, digitale und Online-Programme und Materialien)</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Unterstützung einer strategischen Marketingmentalität durch Förderung unserer Marken, Teilen von Best Practices, Unterstützung der Konsistenz der Umsetzung und Demonstration der Klarheit unserer Marketingstrategie und enge Zusammenarbeit mit dem internationalen Team</li><li style="width:fit-content;" data-end="923" data-start="774" width="fit-content">Verantwortung für die Entwicklung und Ausführung von Plänen zur Einbindung externer Stakeholder in Zusammenarbeit mit funktionsübergreifenden Teams</li><li style="width:fit-content;" data-end="1108" data-start="924" width="fit-content">Taktische Umsetzung – enge Zusammenarbeit mit den kommerziellen und medizinischen Teams, um sicherzustellen, dass die Taktiken relevant und im Einklang mit der Markenstrategie stehen</li><li style="width:fit-content;" data-end="1367" data-start="1109" width="fit-content">Genehmigung von Materialien – Sicherstellung, dass alle Materialien und Aktivitäten den Vorschriften entsprechen, rechtzeitig und von hoher Qualität sind, Zusammenarbeit mit medizinischen und Compliance-Teams und effektive Nutzung von Genehmigungssystemen.</li><li style="width:fit-content;" data-end="1484" data-start="1368" width="fit-content">Überwachung der Umsetzung des taktischen Plans und Berichterstattung über den Fortschritt an den Marketing-Manager</li><li style="width:fit-content;" data-end="1598" data-start="1485" width="fit-content">Wahrung der Unternehmensmission und -werte durch Verantwortung, Innovation, Integrität, Qualität und Teamarbeit</li><li style="width:fit-content;" data-end="1598" data-start="1485" width="fit-content">Marketingplanung – gutes Verständnis der Prinzipien der Marketingstrategie von der Situationsanalyse bis zur taktischen Planung; Fähigkeit, Marketingprioritäten und die Rolle des Marketings innerhalb der Organisation zu artikulieren</li><li style="width:fit-content;" data-end="1598" data-start="1485" width="fit-content">Marketingkanäle – Verständnis der verschiedenen Marketingkanäle; der Rolle von Digital, Werbung und Promotion innerhalb des Marketing-Mix</li></ul>&nbsp;Qualifikation:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li style="width:fit-content;" data-end="2997" data-start="2977" width="fit-content">Bachelor-Abschluss</li><li style="width:fit-content;" data-end="3110" data-start="2998" width="fit-content">5+ Jahre kommerzielle Erfahrung im Gesundheitssektor, idealerweise in einer kommerziellen Rolle in Deutschland</li><li style="width:fit-content;" data-end="3578" data-start="3111" width="fit-content">Erfahrung in:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;" data-end="3578" data-start="3129"><li data-end="3194" data-start="3129">Brand-Planning-Zyklen in der Pharma- oder Medizintechnikbranche</li><li data-end="3293" data-start="3197">Zusammenarbeit mit kommerziellen Außendienstteams und funktionsübergreifenden Therapiegebieten</li><li data-end="3362" data-start="3296">Aufbau von Beziehungen zu HCPs und anderen externen Stakeholdern</li><li data-end="3406" data-start="3365">Kenntnisse relevanter Verhaltenskodizes</li><li data-end="3468" data-start="3409">Kenntnis der Marktstruktur und des Marktes in Deutschland</li><li data-end="3578" data-start="3471">Zusammenarbeit mit Kreativagenturen und anderen externen Partnern zur Unterstützung der Unternehmensziele</li></ul></li><li style="width:fit-content;" data-end="3628" data-start="3579" width="fit-content">Sicherer Umgang mit Microsoft Office-Programmen</li><li style="width:fit-content;" data-end="3683" data-start="3629" width="fit-content">Starke Teamarbeit innerhalb einer Matrixorganisation</li><li style="width:fit-content;" data-end="3756" data-start="3684" width="fit-content">Fähigkeit, eigenständig zu arbeiten und mehrere Zeitpläne zu verwalten</li><li style="width:fit-content;" data-end="3846" data-start="3757" width="fit-content">Hohe Detailgenauigkeit, qualitätsorientiert mit der Fähigkeit, das große Ganze zu sehen</li><li style="width:fit-content;" data-end="3937" data-start="3847" width="fit-content">Ausgezeichnete mündliche, schriftliche und zwischenmenschliche Kommunikationsfähigkeiten</li><li style="width:fit-content;" data-end="3980" data-start="3938" width="fit-content">Sehr gut organisiert und selbstmotiviert</li><li style="width:fit-content;" data-end="4054" data-start="3981" width="fit-content">Starke Fähigkeiten im Stakeholder-Management und Aufbau von Beziehungen</li><li style="width:fit-content;" data-is-last-node data-end="4100" data-start="4055" width="fit-content">Gute Englischkenntnisse in Wort und Schrift</li><li style="width:fit-content;" data-is-last-node data-end="4100" data-start="4055" width="fit-content">Reiseanforderungen: 20%+ Reisebereitschaft</li></ul>&nbsp;Rahmendaten:&nbsp;Start: Ab sofort&nbsp;Dauer: Festanstellung&nbsp;Auslastung: 5 Tage die WocheEinsatzort: Bayern&nbsp;&nbsp;&nbsp;&nbsp;</div>

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;"><div style="--ck-color-selector-caption-background:hsl(0, 0%, 97%);--ck-color-selector-caption-text:hsl(0, 0%, 20%);--ck-image-style-spacing:1.5em;--ck-inline-image-style-spacing:calc(var(--ck-image-style-spacing) / 2);font-family:Segoe UI;font-size:11pt;">&nbsp;Specialist Manufacturing Operations (M/F/D)&nbsp;Tasks:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoListParagraphCxSpFirst" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Set up, practical execution and troubleshooting of upstream, downstream and support unit operations in continuous manufacturing and fed-batch processes under Good Manufacturing Practices (GMP)&nbsp;<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Knowledge of and compliance to GMP principles and EHS standards in the area of responsibility<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Management and documentation of process execution, deviations, changes and CAPAs. Partnering with Quality Assurance and other internal stakeholders during investigations and technical discussions &nbsp;<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Involvement in continuous improvement efforts and support for the implementation of new technologies, including non-GMP engineering runs or testing activities<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Creation and updates of SOPs and (electronic) master batch records. Technical review of various documentation related to process transfer and GMP manufacturing<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Material management using ERP systems (SAP)<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Participation in sampling activities or on-call duties, which may include weekend work<o:p></o:p></li></ul>&nbsp;&nbsp;Qualification:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoListParagraphCxSpFirst" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Educational background in a relevant discipline&nbsp;<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">A minimum of 2-5 years of work experience in the pharmaceutical or biotech industry<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Experience (2-5 years) or educational background in upstream or downstream processing. General knowledge of unit operations in manufacturing processes for biologics and of GMP requirements<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Ability to solve problems and take new perspectives on existing solutions with a desire to continuously learn, improve and develop. Ability to perform under pressure in a complex GMP environment.&nbsp;<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Business Fluent in English and German: Effective oral / written communication skills in English (C1) Oral / written communication skills in German (B1)&nbsp;</li></ul>Preferred Experience and Skills:&nbsp;<o:p></o:p><ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoListParagraphCxSpFirst" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">A bachelor’s or master’s degree in a relevant discipline<o:p></o:p><o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Experience with quality management and compliance systems (Trackwise/SAP QM/VeevaVault)<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Familiarity with the use of automated systems in manufacturing (DeltaV) or electronic batch records (MES)<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Prior experience with process development or process scale-up is beneficial<o:p></o:p></li><li class="MsoListParagraphCxSpLast" style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Ability to work efficiently as part of a team, as well as willingness to take responsibility for independent projects<o:p></o:p></li></ul>&nbsp;&nbsp;Requirements:&nbsp;Start: 03.02.2025Duration: &nbsp;31.12.2026Capacity: 5 days per weekLocation: Werthenstein, Switzerland&nbsp;</div></div>

Specialist Manufacturing Operations

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;"><div style="--ck-color-selector-caption-background:hsl(0, 0%, 97%);--ck-color-selector-caption-text:hsl(0, 0%, 20%);--ck-image-style-spacing:1.5em;--ck-inline-image-style-spacing:calc(var(--ck-image-style-spacing) / 2);font-family:Segoe UI;font-size:11pt;">Senior Controller (M/W/D)&nbsp;Aufgaben:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px; width: fit-content;" width="fit-content" type="disc"><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Übernahme von Ad-Hoc Analysen<o:p></o:p><ul style="list-style-type: circle; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="circle"><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Margenanalyse und Liquiditätsplanung<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Selbständige Einarbeitung in komplexe Sachverhalte wie den Businessplan, der eine integrierte Darstellung und Planung unserer Finanzzahlen darstellt<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Erstellung und Kommentierung des Monatsabschlusses und Budget<o:p></o:p></li></ul></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Gute Kennnisse in Bilanz und GuV<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Gute Kennnisse in der Erstellung einer indirekten Kapitalflussrechnung<o:p></o:p><o:p></o:p></li></ul>&nbsp;Qualifikation:<div style="font-family:Segoe UI;font-size:11pt;"><ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px; width: fit-content;" type="disc" width="fit-content"><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Mindestens 5 Jahre Erfahrung im Controlling<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Idealerweise zusätzliche Erfahrung im Konzernrechnungswesen<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Kenntnisse in SAP S/4 HANA und Lucanet Erfahrungen</li></ul></div></div>&nbsp;Rahmendaten:&nbsp;Start: 01.05.2025Dauer: FestanstellungAuslastung: 5 Tage die WocheEinsatzort: München und Remote&nbsp;&nbsp;</div>

Senior Controller (m/w/d)

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;"><div style="--ck-color-selector-caption-background:hsl(0, 0%, 97%);--ck-color-selector-caption-text:hsl(0, 0%, 20%);--ck-image-style-spacing:1.5em;--ck-inline-image-style-spacing:calc(var(--ck-image-style-spacing) / 2);font-family:Segoe UI;font-size:11pt;">MSL (M/F/D)&nbsp;Tasks:<ul style="list-style-type: disc; margin-bottom: 0in; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0in; padding-inline-start: 40px; width: fit-content;" width="fit-content" type="disc"><li class="MsoListParagraph" style="margin-bottom:0in;margin-right:0in;margin-top:0in;">Field-based consultant supporting the company with its Phase 3 clinical trials in the EU and UK.&nbsp; Primary tasks include the following:<o:p></o:p><ul style="list-style-type: circle; margin-bottom: 0in; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0in; padding-inline-start: 40px;" type="circle"><li class="MsoListParagraph" style="margin-bottom:0in;margin-right:0in;margin-top:0in;">Recruitment of sites to participate in trial, site engagement, site initiation visits&nbsp;<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0in;margin-right:0in;margin-top:0in;">Advise regarding Protocol Design<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0in;margin-right:0in;margin-top:0in;">Facilitate discussions between sites, principal investigators, supplement injection monitors / Rescue Monitors and company personnel in the United States<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0in;margin-right:0in;margin-top:0in;">Provide scientific guidance at key regional and national congresses and, potentially provide medical booth support<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0in;margin-right:0in;margin-top:0in;">Adhere to all company policies and standard procedures&nbsp;</li><li class="MsoListParagraph" style="margin-bottom:0in;margin-right:0in;margin-top:0in;">Comply with all statutory, regulatory and similar legislative requirements applicable to the provision of&nbsp; tasks<o:p></o:p></li></ul></li></ul>&nbsp;Qualification:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Successful track record as MSL in the Pharmaceutical Industry</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Expertise in Clinical Trial Management on a global scale</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Preferably Ophthalmology experience</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Existing network in either France or Italy</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Fluent in English and either French or Italian</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Excellent communication, stakeholder management and organization skills</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Flexible with time zones (mainly CET and EST)</li></ul>&nbsp;Requirements:&nbsp;Start: April 2025Duration: 12 monthsCapacity: 5 days per weekLocation: Italy or France - Remote and onsite at study sites&nbsp;</div></div>

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Key Account Manager (M/W/D)&nbsp;Aufgaben:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Ausbau bestehender Kundenbeziehungen sowie Gewinnung von Neukunden in der Zielgruppe der Krankenhausärzte und -apotheken sowie weiterer Entscheidungsträger im Krankenhaus</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Produktvorstellung,-besprechung: Vorstellung sowie Informationsübermittlung, Bearbeitung von Anfragen zu den Produkten des Unternehmens bei den zugeordneten Kunden</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Accountmanagement: Analyse und eigenverantwortliche professionelle Segmentierung, Konzept- und Projekterstellung für die zugeordneten Accounts/Kunden sowie Durchführung der erforderlichen internen Abstimmungen. Erkennen, Analysieren der Versorgungsstrukturen, selbstständiges Erarbeiten der nötigen Strategien und Schlussfolgerungen</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Budget- und Ressourcenplanung: eigenverantwortliche Planung der verfügbaren Budgets und Ressourcen unter Berücksichtigung der Unternehmensstrategie und regionalen Besonderheiten</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Umsatzverantwortung für die zugeordneten Accounts</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Informationsaustausch/Teamabstimmung: Einhaltung der strategischen und operativen Zielrichtung des Unternehmens. Wissenstransfer und –austausch sowie Zusammenarbeit und Koordination der Aktivitäten im Team sowie mit Kollegen beteiligter Schnittstellenbereiche im Unternehmen vor allem mit den MSL und dem Commercial Team</li></ul>&nbsp;Qualifikation:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Mindestens 3-jährige Erfahrung in der pharmazeutischen Industrie und im Krankenhaus Sektor</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">gesundheitsökonomisches und medizinisches Grundverständnis</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Fundierte Kenntnisse von AMG, HWG und der einschlägigen Compliance-Kodizes</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Profunde Kenntnisse gängiger IT-Anwendungen (MS Office)</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Bereitschaft zu intensiver Reisetätigkeit</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Gute Englischkenntnisse in Wort und Schrift</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">naturwissenschaftliches Studium oder Status Pharmaberater / Pharmareferent (w/m) nach § 75 AMG</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Sehr gute Markt- und Kundenkenntnisse im Krankenhaus Sektor, sowie speziell in den Bereichen Infektiologie, Intensivmedizin und Onkologie</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Fundierte Kenntnisse der gesundheitsökonomischen Entscheidungswege, Erstattungsbedingungen und Strukturen in der Klinik</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Umfangreiche Erfahrungen im Projektmanagement/ Netzwerkarbeit vor allem im Krankenhausbereich</li></ul>&nbsp;Rahmendaten:&nbsp;Start: asap / 01.05Dauer: PERMAuslastung: 5 Tage die WocheEinsatzort: Deutschland&nbsp;&nbsp;&nbsp;</div>

Key Account Manager

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Medical Science Liaison Manager (M/W/D)&nbsp;Aufgaben:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoListParagraph" style="margin-bottom:.0001pt;margin-right:0cm;margin-top:6.0pt;">Identifikation, Selektion, Charakterisierung und kontinuierliche Betreuung von KOLs im jeweiligen Indikationsgebiet. Erste Ansprechperson der KOLs für den wissenschaftli­chen Dialog.</li><li class="MsoListParagraph" style="margin-bottom:.0001pt;margin-right:0cm;margin-top:6.0pt;">Recherche von Versorgungsstrukturen und Leitlinien in Vorbereitung geplanter Produkt­neueinführungen</li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Intensive Literaturrecherche sowie Kongressbesuche mit an­schließender Berichterstat­tung, Identifikation und laufende Beobachtung von Konkurrenzprodukten&nbsp;<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Erstellung von med.-wiss. Präsentationen für Ärzte, nicht-ärztliches Fachpersonal und ggf. Patientenorganisationen, sowie aktive Vortragstätigkeit intern (z. B. Außendienst) und extern (z. B. Klinikärzte)<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Mitarbeit an nationalen und regiona­len Expertentreffen und Referententrainings</li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Regionale Umsetzung von klinischen Projekten (IITs, NIS, Registerstudien)&nbsp; &nbsp;<o:p></o:p></li></ul>Qualifikation:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Mindestens 2-3 Jahre Tätigkeit als MSL</li><li class="MsoListParagraph" style="margin-bottom:6.0pt;margin-right:0cm;margin-top:0cm;">Abgeschlossenes Studium der Medizin, Naturwissenschaften oder Pharmazie, vorzugswei­se mit Promotion&nbsp;<o:p></o:p><o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Berufliche Erfahrung in den Indikationen Infektiologie, Intensivmedizin und Hämato-Onkologie<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Fundierte Kenntnisse von AMG, HWG und der einschlägigen Compliance-Kodizes&nbsp;<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Profunde Kenntnisse gängiger IT-Anwendungen (MS Office), insbes. Power Point&nbsp;<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Sehr gute Englischkenntnisse in Wort und Schrift&nbsp;<o:p></o:p></li><li class="MsoListParagraph" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Bereitschaft zu intensiver Reisetätigkeit (national und international)&nbsp;</li></ul>&nbsp;Rahmendaten:&nbsp;Start: asap&nbsp;Dauer: 3- 12 MonateAuslastung: 5 Tage die WocheEinsatzort: Reisen in D &amp; &nbsp;remote&nbsp;&nbsp;&nbsp;&nbsp;</div>

Medical Science Liaison Manager

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;"><p style="background-color: rgb(255, 255, 255); border-width: 0px; color: rgba(0, 0, 0, 0.9); font-family: -apple-system, system-ui, BlinkMacSystemFont, &quot; undefined: SegoeUI&quot; undefined: ,Roboto,&quot; undefined: HelveticaNeue&quot; undefined: ,&quot; undefined: FiraSans&quot; undefined: ,Ubuntu,Oxygen,&quot; undefined: OxygenSans&quot; undefined: ,Cantarell,&quot; undefined: DroidSans&quot; undefined: ,&quot; undefined: AppleColorEmoji&quot; undefined: ,&quot; undefined: SegoeUIEmoji&quot; undefined: ,&quot; undefined: SegoeUIEmoji&quot; undefined: ,&quot; undefined: SegoeUISymbol&quot; undefined: ,&quot; undefined: LucidaGrande&quot; undefined: ,Helvetica,Arial,sans-serif; font-size: var(--artdeco-reset-typography_getFontSize); font-style: normal; font-weight: 400; letter-spacing: normal; line-height: var(--artdeco-reset-typography_getLineHeight); margin: var(--artdeco-reset-base-margin-zero); padding: var(--artdeco-reset-base-padding-zero); text-indent: 0px; text-transform: none; vertical-align: baseline; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><strong style="border-width:0px;font-size:var(--artdeco-reset-base-font-size-hundred-percent);font-weight:var(--hue-web-font-weight-bold);margin:var(--artdeco-reset-base-margin-zero);outline:var(--artdeco-reset-base-outline-zero);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Key Responsibilities<ul style="background-color: rgb(255, 255, 255); border-width: 0px; color: rgba(0, 0, 0, 0.9); font-family: -apple-system, system-ui, BlinkMacSystemFont, &quot; undefined: SegoeUI&quot; undefined: ,Roboto,&quot; undefined: HelveticaNeue&quot; undefined: ,&quot; undefined: FiraSans&quot; undefined: ,Ubuntu,Oxygen,&quot; undefined: OxygenSans&quot; undefined: ,Cantarell,&quot; undefined: DroidSans&quot; undefined: ,&quot; undefined: AppleColorEmoji&quot; undefined: ,&quot; undefined: SegoeUIEmoji&quot; undefined: ,&quot; undefined: SegoeUIEmoji&quot; undefined: ,&quot; undefined: SegoeUISymbol&quot; undefined: ,&quot; undefined: LucidaGrande&quot; undefined: ,Helvetica,Arial,sans-serif; font-size: var(--artdeco-reset-typography_getFontSize); font-style: normal; font-weight: 400; letter-spacing: normal; line-height: var(--artdeco-reset-typography_getLineHeight); margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; padding-left: 18px; text-align: start; text-indent: 0px; text-transform: none; vertical-align: baseline; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Develop reimbursement strategies aligned with the French healthcare system, focusing on mechanisms such as T2A, CCAM, and innovation support programs (e.g., Forfait Innovation).</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Navigate public funding opportunities like PIA (Programme d’Investissements d’Avenir) or grants from ARS (Agence Régionale de Santé).</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Liaise with CNAM, HAS (Haute Autorité de Santé), and regional agencies for regulatory approvals and funding discussions.</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Conduct detailed market analysis to identify and optimize funding/reimbursement pathways for MedTech solutions.</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Collaborate with hospitals and other healthcare providers to prepare and submit applications for reimbursement and public funding programs.</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Keep up-to-date with changes in national healthcare policies, reimbursement structures, and funding opportunities.</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Provide strategic advice on financial and operational feasibility for healthcare institutions adopting our Clients solutions.</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Produce high-quality reports, presentations, and documentation for internal and external stakeholders.</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Deliver projects on time and within scope while maintaining a focus on quality and compliance.</li></ul><p style="background-color: rgb(255, 255, 255); border-width: 0px; color: rgba(0, 0, 0, 0.9); font-family: -apple-system, system-ui, BlinkMacSystemFont, &quot; undefined: SegoeUI&quot; undefined: ,Roboto,&quot; undefined: HelveticaNeue&quot; undefined: ,&quot; undefined: FiraSans&quot; undefined: ,Ubuntu,Oxygen,&quot; undefined: OxygenSans&quot; undefined: ,Cantarell,&quot; undefined: DroidSans&quot; undefined: ,&quot; undefined: AppleColorEmoji&quot; undefined: ,&quot; undefined: SegoeUIEmoji&quot; undefined: ,&quot; undefined: SegoeUIEmoji&quot; undefined: ,&quot; undefined: SegoeUISymbol&quot; undefined: ,&quot; undefined: LucidaGrande&quot; undefined: ,Helvetica,Arial,sans-serif; font-size: var(--artdeco-reset-typography_getFontSize); font-style: normal; font-weight: 400; letter-spacing: normal; line-height: var(--artdeco-reset-typography_getLineHeight); margin: var(--artdeco-reset-base-margin-zero); padding: var(--artdeco-reset-base-padding-zero); text-indent: 0px; text-transform: none; vertical-align: baseline; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><strong style="border-width:0px;font-size:var(--artdeco-reset-base-font-size-hundred-percent);font-weight:var(--hue-web-font-weight-bold);margin:var(--artdeco-reset-base-margin-zero);outline:var(--artdeco-reset-base-outline-zero);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Qualifications:<ul style="background-color: rgb(255, 255, 255); border-width: 0px; color: rgba(0, 0, 0, 0.9); font-family: -apple-system, system-ui, BlinkMacSystemFont, &quot; undefined: SegoeUI&quot; undefined: ,Roboto,&quot; undefined: HelveticaNeue&quot; undefined: ,&quot; undefined: FiraSans&quot; undefined: ,Ubuntu,Oxygen,&quot; undefined: OxygenSans&quot; undefined: ,Cantarell,&quot; undefined: DroidSans&quot; undefined: ,&quot; undefined: AppleColorEmoji&quot; undefined: ,&quot; undefined: SegoeUIEmoji&quot; undefined: ,&quot; undefined: SegoeUIEmoji&quot; undefined: ,&quot; undefined: SegoeUISymbol&quot; undefined: ,&quot; undefined: LucidaGrande&quot; undefined: ,Helvetica,Arial,sans-serif; font-size: var(--artdeco-reset-typography_getFontSize); font-style: normal; font-weight: 400; letter-spacing: normal; line-height: var(--artdeco-reset-typography_getLineHeight); margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; padding-left: 18px; text-align: start; text-indent: 0px; text-transform: none; vertical-align: baseline; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Certification in project management (e.g., PMP, PRINCE2).</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Familiarity with a great variety of MedTech products.</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Experience engaging with government agencies, such as HAS (France) or INEK/KV (Germany).</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Knowledge of digital health or SaaS applications in the healthcare space.</li><li style="border-width:0px;color:rgba(0, 0, 0, 0.9);font-size:var(--artdeco-reset-typography_getFontSize);font-weight:var(--artdeco-reset-typography-font-weight-normal);line-height:var(--artdeco-reset-typography_getLineHeight);padding:var(--artdeco-reset-base-padding-zero);vertical-align:baseline;">Proficiency in relevant languages (French for France-based role; German for Germany-based role) and fluency in English.</li></ul>&nbsp;<div style="--ck-color-selector-caption-background:hsl(0, 0%, 97%);--ck-color-selector-caption-text:hsl(0, 0%, 20%);--ck-image-style-spacing:1.5em;--ck-inline-image-style-spacing:calc(var(--ck-image-style-spacing) / 2);font-family:Segoe UI;font-size:11pt;">Further Details: Start: Asap (latest March)Duration: tbd.Capacity: At least 20 hours/weekLocation: Remote &amp; <span style="background-color:rgb(255,255,255);color:rgba(0,0,0,0.9);font-family:-apple-system, system-ui, BlinkMacSystemFont, &quot;Segoe UI&quot;, Roboto, &quot;Helvetica Neue&quot;, &quot;Fira Sans&quot;, Ubuntu, Oxygen, &quot;Oxygen Sans&quot;, Cantarell, &quot;Droid Sans&quot;, &quot;Apple Color Emoji&quot;, &quot;Segoe UI Emoji&quot;, &quot;Segoe UI Emoji&quot;, &quot;Segoe UI Symbol&quot;, &quot;Lucida Grande&quot;, Helvetica, Arial, sans-serif;font-size:14px;"><span style="display:inline !important;float:none;font-style:normal;font-weight:400;letter-spacing:normal;text-align:start;text-indent:0px;text-transform:none;white-space:normal;width:fit-content;word-spacing:0px;" width="fit-content">Île-de-France Region</div></div>

Reimbursement Specialist Medical Devices France

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;"><div style="--ck-color-selector-caption-background:hsl(0, 0%, 97%);--ck-color-selector-caption-text:hsl(0, 0%, 20%);--ck-image-style-spacing:1.5em;--ck-inline-image-style-spacing:calc(var(--ck-image-style-spacing) / 2);font-family:Segoe UI;font-size:11pt;">Sales Manager (M/W/D)&nbsp;Aufgaben:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li style="width:fit-content;" width="fit-content">Gezielte Einführung und Verbreitung unseres innovativen Produktportfolios innerhalb der bestehenden Kundenbasis, sowohl auf internationaler als auch auf lokaler Ebene</li><li style="width:fit-content;" width="fit-content">Aufbau und Pflege langfristiger, nachhaltiger Kundenbeziehungen</li><li style="width:fit-content;" width="fit-content">Akquisition neuer Kunden und Geschäftspartner zur Erweiterung des Kundenstamms</li><li style="width:fit-content;" width="fit-content">Beratung und Betreuung von Kunden und Partnern auf professionellem Niveau</li><li style="width:fit-content;" width="fit-content">Analyse von Märkten unter Berücksichtigung länderspezifischer Gegebenheiten</li><li style="width:fit-content;" width="fit-content">Engagement in der Teilnahme an Messen, Kongressen und Fachevents</li><li style="width:fit-content;" width="fit-content">Aktive Unterstützung und Mitgestaltung bei der Durchführung und Weiterentwicklung von Vertriebsprojekten</li><li style="width:fit-content;" width="fit-content">Erstellung von Verkaufsberichten sowie regelmäßige Pflege und Aktualisierung von Kundendaten im CRM-System</li><li style="width:fit-content;" width="fit-content">Entwicklung von Angeboten, Preisvorschlägen und Vertragsentwürfen</li></ul>&nbsp;Qualifikation:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li style="width:fit-content;" width="fit-content">Vertriebs-Erfahrung in der medizinischen oder pharmazeutischen Industrie</li><li style="width:fit-content;" width="fit-content">Abgeschlossenes Studium in Pharmazie, Naturwissenschaften oder Wirtschaft mit fundierter Erfahrung im medizinischen oder pharmazeutischen Bereich</li><li style="width:fit-content;" width="fit-content">Verhandlungskompetenz, ausgeprägte Kundenorientierung und hohe Zuverlässigkeit</li><li style="width:fit-content;" width="fit-content">Fähigkeit, komplexe Sachverhalte klar und verständlich zu erklären</li><li style="width:fit-content;" width="fit-content">Sehr gute Deutschkenntnisse sowie fließende Englischkenntnisse in der Geschäftskommunikation</li><li style="width:fit-content;" width="fit-content">Sicherer Umgang mit MS Office, insbesondere Excel und PowerPoint</li><li style="width:fit-content;" width="fit-content">Teamorientierung, Flexibilität, Belastbarkeit und eine eigenständige Arbeitsweise</li><li style="width:fit-content;" width="fit-content">Bereitschaft zu regelmäßigen Dienstreisen</li></ul>&nbsp;Rahmendaten:&nbsp;Start: asapDauer: unbefristetAuslastung: 40h pro WocheEinsatzort: München und remote</div></div>

Sales Manager

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Automation Engineer (M/W/D)&nbsp;Aufgaben:<ul class="text-element-body_text" style="background-color: rgb(255, 255, 255); color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-style: normal; font-weight: 400; letter-spacing: normal; line-height: 1.5em; margin-bottom: 14px; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0px; padding-inline-start: 40px; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Sicherstellen des Produktionsbetriebs, durch Störungs- und Fehleranalyse laufender Systeme</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Unterstützen bei der Kommunikation zum Manufacturing Execution System (MES)&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Unterstützung bei der Anforderungserhebung, Durchführung und Auswertung von technischen Projekten aus Sicht der Automation&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Kontinuierliche Anlagenverbesserung durch Analyse der bestehenden Programmierung unter Berücksichtigung gültiger Normen und anerkannter Regeln der Technik &nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">GMP-gerechte Dokumentation, zusammen mit den entsprechenden abteilungsinternen Stellen, sowie in Abstimmung mit der Qualitätssicherung&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Erarbeitung und Verschriftlichung von System- und Prozess-Know-how sowie Aufbereitung der Dokumentation für SOPs und Mitarbeiterschulungen&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Bearbeitung von CAPAs/DEVs/Changes im Verantwortungsbereich&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Computersystemvalidierung (CSV) vorhandener und neuer Systeme entsprechend GMP vorgaben&nbsp;</li></ul>&nbsp;Qualifikation:<ul class="text-element-body_text" style="background-color: rgb(255, 255, 255); color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-style: normal; font-weight: 400; letter-spacing: normal; line-height: 1.5em; margin-bottom: 14px; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0px; padding-inline-start: 40px; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Abgeschlossenes ingenieurwissenschaftliches Studium mit technischer Fachrichtung in Automatisierungstechnik, Elektrotechnik, Informatik oder artverwandte Ausbildungen&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Gute Kenntnisse der gängigen Automatisierungssystemen der Siemens Familie (PCS7/WinCC/TIA Portal/MES)&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Erweiterte Kenntnisse in der Computersystemvalidierung&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Grundkenntnisse der IT/OT&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Selbstständiges Arbeiten&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Kommunikationsstärke und Organisationsgeschick&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Fließende Deutsch- und Englischkenntnisse&nbsp;</li></ul>&nbsp;Rahmendaten:&nbsp;Start: asapDauer: FestanstellungAuslastung: 5 Tage die WocheEinsatzort: München&nbsp;&nbsp;&nbsp;</div>

Automation Engineer (m/w/d)

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Group Lead Automation (M/W/D)&nbsp;Aufgaben:<ul class="text-element-body_text" style="background-color: rgb(255, 255, 255); color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-style: normal; font-weight: 400; letter-spacing: normal; line-height: 1.5em; margin-bottom: 14px; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0px; padding-inline-start: 40px; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Fachliche und disziplinarische Leitung, sowie Entwicklung der Automations-Gruppe, inklusive der IT/OT (Einarbeitung, Schulungen, Aufgabenverteilung, Zielsetzung und Leistungsmanagement)&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Zentraler Ansprechpartner für den Bedarf an Automationslösungen&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Sicherstellen des zuverlässigen Betriebs der Automationssysteme inklusive der IT/OT Infrastruktur durch beispielsweise wiederkehrende Instandhaltungsmaßnahmen, oder Troubleshooting bei Störungen (gemäß internem Service Level Agreement), in Zusammenarbeit mit den verantwortlichen Abteilungen&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Sicherstellen der Anwendung gültiger Normen und anerkannten Regeln der Technik im Verantwortungsbereich (z.B. GMP, GAMP)&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Garantieren einer technischen und den GMP-Anforderungen entsprechenden Dokumentation&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Garantieren und bedarfsweise aktives Entwickeln von effizienten administrativen und organisatorischen Prozessen im Verantwortungsbereich&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Koordination externer Dienstleister und Kooperationspartner&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Sicherstellen von Qualifizierungen der Systeme im Verantwortungsbereich und der Umsetzung der CSV (Computer System Validation)&nbsp;</li></ul>&nbsp;Qualifikation:<ul class="text-element-body_text" style="background-color: rgb(255, 255, 255); color: rgb(0, 0, 0); font-family: &quot; undefined: OpenSans&quot; undefined: ,sans-serif; font-size: 14px; font-style: normal; font-weight: 400; letter-spacing: normal; line-height: 1.5em; margin-bottom: 14px; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0px; padding-inline-start: 40px; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; width: fit-content; word-spacing: 0px;" width="fit-content"><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Abgeschlossenes Studium zum Ingenieur im Bereich Automatisierungstechnik oder Elektrotechnik oder ein technisches Studium in Verbindung mit entsprechenden Detailkenntnissen in der Automatisierungstechnik &nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Idealerweise Berufserfahrung im Bereich der pharmazeutischen Industrie&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Gute Kenntnisse der gängigen Automatisierungssystemen der Siemens Familie (PCS7/WinCC/TIA Portal/MES) wünschenswert</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Sicherer Umgang mit den CSV-Richtlinien&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Führungskompetenz sowohl im Hinblick auf externe Dienstleister als auch in der Automationsgruppe&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Teamfähigkeit und Kommunikationsstärke kennzeichnen den Arbeitsstil&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Hands-on Mentalität &nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Sicherer Umgang mit MS-Office-Produkten&nbsp;</li><li style="line-height:1.5em;margin-bottom:0.5em;margin-top:0.5em;">Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift&nbsp;</li></ul>&nbsp;Rahmendaten:&nbsp;Start: asapDauer: FestanstellungAuslastung: 5 Tage die WocheEinsatzort: München&nbsp;&nbsp;</div>

Group Lead Automation

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Regulatory Affairs Expert Veterinärmedizintechnik (M/W/D)&nbsp;Aufgaben:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Analyse des bestehenden Produktportfolios im Bereich der Humanmedizintechnik zur Überführung in den Bereich Veterinärmedizintechnik (Risikoklassen I-III)</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Entwicklung und Umsetzung einer Regulatory-Strategie für den deutschen Veterinärmarkt (Zulassung, Labelling, klinische Bewertung) inklusive Behördenkontakt</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Erarbeitung und Sicherstellung der notwendigen Kennzeichnungen für Produkte in der Veterinärmedizintechnik</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Aufbau und Optimierung regulatorischer Prozesse in Zusammenarbeit mit einem interdisziplinären Team und externen Zulieferern</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Sicherstellung der Produktsicherheit und klinischen Bewertung bei tiermedizinischen Anwendungen</li></ul>&nbsp;Qualifikation:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li style="width:fit-content;" width="fit-content">Abgeschlossenes Studium in Medizin, Veterinärmedizin, Biowissenschaften, Ingenieurwesen o.ä.</li><li style="width:fit-content;" width="fit-content">Mehrjährige Erfahrung im Bereich Regulatory Affairs, idealerweise mit Kenntnissen in der Veterinärmedizintechnik sowie in verwandten Bereichen der Humanmedizin</li><li style="width:fit-content;" width="fit-content">Fundierte Kenntnisse nationaler und internationaler Regulierungsstandards (EU-MDR, ISO, BVL)</li><li style="width:fit-content;" width="fit-content">Erfahrung mit Zulassungsprozessen in den USA und/oder UK ist ein Plus</li></ul>&nbsp;Rahmendaten:&nbsp;Start: Ideal 01.03 // Spätestens 30.04Dauer: 6 MonateAuslastung: 2,5 Tage die WocheEinsatzort: Remote + gelegentlich vor Ort in Baden-Württemberg</div>

Regulatory Affairs Expert Veterinärmedizintechnik

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">DevOps Engineer (M/F/D)&nbsp;Tasks:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li>Development and presentation of DevOps concepts (Spikes)<o:p></o:p></li><li>Implementation and testing of defined and committed PI Objectives including it´s related technical tasks e.g. pipeline templates, central monitoring &amp; logspace &amp; VWAN &amp; API Mgmt &amp; Platform Hub&nbsp;<o:p></o:p></li><li>Continues improvements / maintenance of such implementations &amp; infrastructure in terms of costs, efficiency, performance &amp; productivity<o:p></o:p></li><li>Support during deployment and roll-out and data migration of HDP products in the relevant Azure regions<o:p></o:p></li><li>Relevant tools: Azure DevOps (pipelines, repos, artifacts, keyvault), Docker, Terraform, Grafana – Prometheus, ArgoCD, Git, Kubernetes<o:p></o:p></li><li>Implementation tasks established within the agile frameworks such as Scrum, Kanban, and SAFe.<o:p></o:p></li></ul>&nbsp;Qualification:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li>At least 5 years in software development or IT roles with a strong focus on DevOps practices.<o:p></o:p></li><li>A minimum of 2 years of DevOps engineer experience.<o:p></o:p></li><li>Excellent communication and interpersonal abilities to effectively interact with various teams.<o:p></o:p></li><li>Deep understanding of DevOps practices, including CI/CD, automation, infrastructure as code, containerization (Docker, Kubernetes), monitoring and logging, Agile frameworks such as Scrum, Kanban, and SAFe.<o:p></o:p></li><li>Experience with Azure DevOps, Terraform, Grafana/Prometheus, Kubernetes, Argo CD, VNET, Azure Cost Optimization.<o:p></o:p></li></ul>&nbsp;Requirements:&nbsp;Start: 15.02.25, latest 03.03.25Duration: 6 monthsCapacity: 5 days per weekLocation: Fully Remote&nbsp;</div>

DevOps Engineer

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;">Senior Manufacturing Specialist (M/F/D)&nbsp;Tasks:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li>&nbsp;Acts as Subject Matter Expert on manufacturing equipment and processes</li><li>&nbsp;Participates in Tech transfer activities as needed</li><li>Authors related technical instructions and records, including RG/RT, procedures, work instructions, and forms</li><li>Initiates, owns, and manages Manufacturing focused Change Controls, CAPAs, and Planned Exceptions.&nbsp;Supports in generating area assessments and performs root cause investigations in DEV/AA/RAR reports in Trackwise</li><li>The incumbent can be both a people manager,&nbsp;as well as individual contributor with respect to technical instruction management for specific portions of a manufacturing process</li><li>Creates projects as needed to establish new manufacturing techniques to resolve day to day issues with management guidance and cross-functional buy-in</li><li>Utilizes depth of experience and known precedent to identify, troubleshoot, and resolve moderately complex technical and operational problems that arise<span style="mso-ansi-language:EN-US;mso-bidi-font-family:&quot;Times New Roman&quot;;mso-bidi-language:AR-SA;mso-fareast-font-family:&quot;MS Gothic&quot;;mso-fareast-language:EN-US;width:fit-content;" lang="EN-US" width="fit-content">.</li></ul>&nbsp;Qualification:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">8-years of direct experience working in a GMP environment</li><li class="MsoListParagraphCxSpFirst" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;tab-stops:18.9pt;">Coaching and Trainer skills for Manufacturing related activities<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;tab-stops:18.9pt;">Deputy function for MTO Manager role<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;tab-stops:18.9pt;">High knowledge of business and manufacturing processes to support manufacturing operations.<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;tab-stops:18.9pt;">High knowledge of Manufacturing Systems (DeltaV, Syncade, SIMCA, PI, Oracle, TrackWise, etc.)<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;tab-stops:18.9pt;">Very good understanding of the basic QA and cGMP principles<o:p></o:p></li><li class="MsoListParagraphCxSpLast" style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;mso-list:l0 level1 lfo1;tab-stops:18.9pt;">Very good level of technical writing skills<o:p></o:p></li></ul>&nbsp;Requirements:&nbsp;Start: 03.03.2025Duration: 12 monthsCapacity: 5 days per weekLocation: Solothurn, Switzerland&nbsp;</div>

Senior Manufacturing Specialist

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;"><div style="--ck-color-selector-caption-background:hsl(0, 0%, 97%);--ck-color-selector-caption-text:hsl(0, 0%, 20%);--ck-image-style-spacing:1.5em;--ck-inline-image-style-spacing:calc(var(--ck-image-style-spacing) / 2);font-family:Segoe UI;font-size:11pt;">Field Sales Representative (M/W/D)&nbsp;Aufgaben:<div class="ck-content stickystyles-wrapper-insert" style="font-family:Segoe UI,'Segoe UI','Helvetica Neue',sans-serif;font-size:11pt;width:fit-content;" width="fit-content" data-wrapper="true" dir="ltr"><ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li>Informieren und beraten der Ärzte und Apotheken im Vertriebsgebiet zum medizinischen Cannabis mit dem Ziel eines besseren Verständnisses, einer sicheren Handhabung und einer adäquaten Verordnung zur Erhöhung des Absatzes der Produkte in Apotheken</li><li>Indikation/Zielgruppe: in erster Linie Allgemeinmediziner, Neurologen, Schmerztherapeuten und Apotheken</li><li>Selbständiges bereisen des zugeordneten regionalen Gebiets</li><li>Planen, koordinieren und durchführen von Maßnahmen zur Erreichung des vereinbarten Vertriebsziels im eigenen Vertriebsgebiet</li><li>Aufbauen langfristiger, vertrauensvoller Beziehungen zu Ärzten und Apothekern</li><li>Selbständiges durchführen von Fort- und Weiterbildungen in Arztpraxen und Apotheken</li><li>Regelmäßige Analyse der Absatz- und Umsatzentwicklung in Vertriebsgebiet</li><li>Identifikation von Umsatzpotentialen</li><li>Dokumentation der Besuche im CRM-System</li><li>Regelmäßige Teilnahme an überregionalen Messen und Tagungen</li><li>Selbständige Erstellung der Tourenplanung</li><li>Berichten der Entwicklungen im Markt und Aktivitäten des Wettbewerbs</li></ul></div>&nbsp;Qualifikation:<div class="ck-content stickystyles-wrapper-insert" style="font-family:Segoe UI,'Segoe UI','Helvetica Neue',sans-serif;font-size:11pt;width:fit-content;" width="fit-content" data-wrapper="true" dir="ltr"><ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px;"><li>Pharmaberater nach § 75 AMG oder eine vergleichbare Qualifikation, die Sie dazu berechtigt den Beruf eines Pharmaberaters auszuüben</li><li>Verkaufserfahrung mit pharmazeutischen/medizinischen Produkten, mindestens 3 Jahre und nach Möglichkeit im Bereich Schmerz oder MS</li><li>Sehr ergebnis- und zielorientierte Arbeitsweise</li><li>Hohe Verlässlichkeit und Eigenmotivation</li><li>Reisebereitschaft</li></ul></div>&nbsp;Rahmendaten:&nbsp;Start: ab sofort möglichVertragsart: FestanstellungAuslastung: VollzeitEinsatzort: Süd-, Mitte-, Nord-, Ostdeutschland</div></div>

Field Sales Representative

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); --ck-color-selector-caption-background: hsl(0, 0%, 97%); --ck-color-selector-caption-text: hsl(0, 0%, 20%); font-family: Segoe UI; font-size: 11pt;"><div style="--ck-color-selector-caption-background:hsl(0, 0%, 97%);--ck-color-selector-caption-text:hsl(0, 0%, 20%);--ck-image-style-spacing:1.5em;--ck-inline-image-style-spacing:calc(var(--ck-image-style-spacing) / 2);font-family:Segoe UI;font-size:11pt;">Entwicklungsingenieur</div>&nbsp;Aufgaben:<ul style="list-style-type: disc; margin-bottom: 0cm; margin-inline-end: 0px; margin-inline-start: 0px; margin-top: 0cm; padding-inline-start: 40px;" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Entwicklung von Instrumenten zur chirurgischen Anwendung und Unterstützung bei der Zulassung in der EU (MDR, IEC 60601), USA (FDA) und weiteren internationalen Zulassungsstellen</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Durchführung von Anwendungsversuche an tierischem Gewebe und technische Versuche zur normativen Übereinstimmung und Dokumentation der Ergebnisse</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Laborarbeit: Bewertung der Kompatibilität der Instrumente zu den Generatoren, prarametrieren eigener Generatoren und Durchführung von Versuchen nach Kundenreklamationen</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Erstellung der technischen Dokumentation für Medizinprodukte und Unterstützung bzgl. technischen und normativen Anforderungen an die Instrumente</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:15px;line-height:normal;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Definition von Produktanforderungen von Instrumenten, Generatoren und Systemen in Zusammenarbeit mit Systems Engineering und Verifikation</li></ul>&nbsp;Qualifikation:<ul style="margin-inline-end: 0px; margin-inline-start: 0px; padding-inline-start: 40px; width: fit-content;" width="fit-content"><li class="MsoListParagraphCxSpFirst" style="line-height:107%;margin-bottom:0in;margin-right:0in;margin-top:0in;">Abgeschlossenes Studium der Elektrotechnik, Physik oder Medizintechnik<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:107%;margin-bottom:0in;margin-right:0in;margin-top:0in;">Begleitung von Entwicklungsprojekten in der HF-Chirurgie<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:107%;margin-bottom:0in;margin-right:0in;margin-top:0in;">Kenntnisse der geltenden Normen wichtiger Märkte (EU und USA)<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:107%;margin-bottom:0in;margin-right:0in;margin-top:0in;">Bereitschaft zum Testen von Instrumenten an tierischem Gewebe<o:p></o:p></li><li class="MsoListParagraphCxSpMiddle" style="line-height:107%;margin-bottom:0in;margin-right:0in;margin-top:0in;">Schnelle Informationsaufnahme und -verarbeitung<o:p></o:p></li><li class="MsoListParagraphCxSpLast" style="line-height:107%;margin-bottom:8pt;margin-right:0in;margin-top:0in;">Sehr gute Deutsch- und Englischkenntnisse<o:p></o:p></li></ul>&nbsp;Rahmendaten:&nbsp;Start: asapDauer: unbefristete FestanstellungAuslastung: 5 Tage die WocheEinsatzort: BaWü (vor Ort + Remote)&nbsp;&nbsp;&nbsp;</div>