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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.

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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.

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I would like to be included in the K-Recruiting freelancer pool. This will give me the opportunity to receive further exciting offers. By being included in the freelancer 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.


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<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); font-family: Arial; font-size: 11pt;">IT Expert (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0cm; margin-top: 0cm;" 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;">Seeking an experienced Customer Service professional to support the Commercial stream (SAP SD) of the Lean Digital Core (LDC) program</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;">This role is supporting the new SAP module and associated processes are validated from a business perspective and meet operational readiness for go-live in January 2026</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 the coordination and execution of User Acceptance Testing (UAT) activities for the Customer Service (Commercial) function</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;">Collaborate with global and local stakeholders to define and validate test scenarios, scripts, and acceptance criteria</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;">Validate SAP system functionality against business requirements, including integration points with SCM and Finance</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;">Identify, document, and escalate defects or gaps in functionality, and support resolution tracking</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 / represent Customer Service in daily UAT stand-ups and defect triage meetings. &nbsp;</li></ul>Qualification:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0cm; margin-top: 0cm;" 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;">Strong knowledge and background on SAP and IT // Could be someone who worked several years for and on SAP</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;">Experienced admin professional; hands-on mindset</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 fluent /native - German nice to have</li></ul>&nbsp;Requirements:&nbsp;Start: 18.08.2025Duration: 6 monthsCapacity: 5 days per week (1-2 days remote possible)Location: Rotkreuz, Switzerland&nbsp;&nbsp;</div>

IT Expert

<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); font-family: Arial; font-size: 11pt;">Quality Control Specialist (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside; list-style-type: disc;"><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Review and approve Master batch records and ensure conformance to all applicable policies/procedure and compliance with all governing regulations.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Manage routine and complex deviations</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Support process and analytical change requests.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Assist the maintenance of retention samples, ship reagents and samples to support licensure and foreign registration; responsible for shipment under quarantine.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Support routine process validation; review and approve validation reports/tech transfer</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Prepare pre-PAI assessments; support document requests for regulatory filings and post approval changes.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Regular site visits to build relationships and monitor efforts to improve the external manufacturer’s quality and reliability through ongoing oversight and formal communication programs and forums.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Previous experience in the pharmaceutical industry with thorough knowledge of Quality Systems, Quality Assurance, and Quality Control including global GMP Quality Systems and</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Review and approve Master batch records and ensure conformance to all applicable policies/procedure and compliance with all governing regulations.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Manage routine and complex deviations</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Support process and analytical change requests.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Assist the maintenance of retention samples, ship reagents and samples to support licensure and foreign registration; responsible for shipment under quarantine.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Support routine process validation; review and approve validation reports/tech transfer</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Prepare pre-PAI assessments; support document requests for regulatory filings and post approval changes.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Regular site visits to build relationships and monitor efforts to improve the external manufacturer’s quality and reliability through ongoing oversight and formal communication programs and forums.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Previous experience in the pharmaceutical industry with thorough knowledge of Quality Systems, Quality Assurance, and Quality Control including global GMP Quality Systems andregulatory requirements preferred</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside; list-style-type: disc; padding-left: 4px;"><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Solves complex problems; takes a new perspective using existing solutions.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Works independently, receives minimal guidance.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Acts as a resource for colleagues with less experience within own discipline; can provide minimal guidance on issue resolution and act as SME.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">May act as a team or project lead and lead work of others as required; promotes teamwork and open discussion of issues, coaches and guides others.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Explains difficult issues and works to build alignment around a complex situation.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Ability to work across boundaries; demonstrated interpersonal, relationship building and leadership skills.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Strong knowledge of External Manufacturing management, supply chain, and operations.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Fluent in English, German language skills are of advantage</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Nice to have: </li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Direct experience with managing external partners.</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Experience with manufacturing operations and/or analytical expertise associated with</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">biologics and/or vaccines. </li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Previous experience with regulatory communications such as Biologics License Applications</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">(BLAs), New Drug Applications (NDAs)</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Degree in Science, Engineering or any relevant technical discipline (BS Biology, Microbiology, Pharmacy, Chemistry, Chemical Engineering, or equivalent preferred).</li><li style="margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Previous experience in the pharmaceutical industry with thorough knowledge of Quality Systems, Quality Assurance, and Quality Control including global GMP Quality Systems and regulatory requirements preferred</li></ul>&nbsp;Requirements:&nbsp;Start: 01.09.2025Duration: 12 monthsCapacity: 5 days per weekLocation: Lucerne, Switzerland&nbsp;</div>

Quality Control 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); font-family: Arial; font-size: 11pt;">Validation Engineer (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0cm; margin-top: 0cm;" 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;"><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="-webkit-text-stroke-width:0px;display:inline !important;float:none;font-style:normal;font-variant-caps:normal;font-variant-ligatures:normal;font-weight:400;letter-spacing:normal;orphans:2;text-align:left;text-decoration-color:initial;text-decoration-style:initial;text-decoration-thickness:initial;text-indent:0px;text-transform:none;white-space:normal;widows:2;word-spacing:0px;">Backgroung : New aspectic area project</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;">Step : commissioning and qualification</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 of SAT execution protocole, perform IOQ report ( leverage approach)</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;">Execution of cycle development and Performance qualification protocols for:</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;">Cleaning validation : writting protocol, execution including rinse water and surface sampling, final report writting</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;">Sterilization validation : writting protocol, execution including placement of thermocouples (using Kaye systgem) and bioindicators, final report writting.&nbsp;</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0cm; margin-top: 0cm;" 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;">French and English (fluent) </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;">Digital system Kneat is using for all 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;">Working hours : daily basis, possibility to work on shift (2*8) when applicable, work on site</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;">Flexibile, team worker</li></ul>&nbsp;Requirements:&nbsp;Start: asapDuration: 4 monthsCapacity: 5 days per weekLocation: Neuchatel, Switzerland&nbsp;</div>

Validation 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); font-family: Arial; font-size: 11pt;">Regulatory Affairs Manager (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside;"><li data-end="383" data-start="125">Defines, develops, and supports regional regulatory strategies (EUCAN or GEM) to maximize regulatory success, support product development, and enable timely patient access through investigational applications, market approvals, and life-cycle management.</li><li data-end="592" data-start="384">Collaborates closely with global, regional, and local teams to align on program objectives and ensure full compliance with applicable regulatory requirements throughout product development and life-cycle.</li><li data-end="761" data-start="593">Leads or supports Submission Working Groups and represents the region on global and project teams, coordinating regulatory activities across the product life cycle.</li><li data-end="971" data-start="762">Maintains up-to-date knowledge of regional regulations and guidance, assessing their impact on drug development, registration, and post-marketing commitments to optimize regulatory outcomes and compliance.</li><li data-end="1175" data-start="972">Provides regulatory expertise for drug development, registration, post-marketing compliance, and life-cycle management, including authoring and reviewing internal procedures and regulatory documents.</li><li data-end="1408" data-start="1176">Develops strong working relationships with internal teams, consultants, business partners, and health authorities, supporting effective communication of regulatory strategies, submission plans, and health authority interactions.</li><li data-end="1643" data-start="1409">Oversees and actively manages interactions with Health Authorities in EUCAN and GEM regions, preparing for and representing the company in meetings, communicating outcomes, and ensuring timely regulatory submissions and approvals.</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0cm; margin-top: 0cm;" 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;">BSc. Advanced scientific related degree preferred; BA accepted based on 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;">A minimum of 4 years of experience in drug regulatory affairs preferably within the EU/GEM region.</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;">Experience with advanced therapeutic medical products (Cell &amp; gene therapy) will be advantageous.</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;">Solid regulatory experience, including knowledge of regulations and guidance governing drugs and biologics in all phases of development for [Emerging markets and/or EUCAN Markets (relevant to role)] as well as leading interaction with Health Authorities.</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;">Has basic regulatory procedure knowledge with major health authorities in the region</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 issues with attention to detail and makes reasoned recommendation</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;">Promotes an inclusive culture and expresses empathy for others</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;">Is able to carry out assigned activities within reasonable time</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;">Fluency in English</li></ul>&nbsp;Requirements:&nbsp;Start: 15.09.2025Duration: 6 monthsCapacity: 5 days per weekLocation: Zurich, Switzerland&nbsp;</div>

Regulatory Affairs 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); font-family: Arial; font-size: 11pt;">SAP Integration Consultant (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Technical consulting on integration scenarios and middleware components (SAP BTP, CPI, Cloud ALM)</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Comprehensive documentation of the integration architecture and technology landscape</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Execute specific technology adjustments or changes within clearly scoped project assignments, particularly in complex integration scenarios.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Implement defined technical changes in coordination with the project team, without assuming overarching coordination responsibilities.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Advise on translating business requirements into technical solution proposals.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Consulting the implementation of an ERP technology landscape focused on S/4 HANA, within the scope of project-related tasks.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Consider existing change management procedures when executing technical changes in the SAP environment.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Provide project-related status updates on assigned work packages, without regular reporting obligations.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Offer technical consulting on middleware components such as SAP BTP (including CPI) and Cloud ALM, especially in the context of monitoring and integration.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Guide the handover of project deliverables to production, including technical consulting during the go-live phase.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Provide expert input for 2nd-level support of defined applications, with the goal of facilitating a structured transition to external partners.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Collaborate with internal contacts on technical issue analysis, strictly within the scope of defined project tasks.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Advise on the development of the SAP technology landscape, including optimization suggestions, without strategic responsibility.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Consulting security-related aspects of application integration in coordination with SAP Basis, within the scope of technical consulting.</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Ability to analyse very complex situations in unknown environments</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Strong communication and collaboration skills</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Prioritization skills and experience</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Knowledge of GMP, SOX and GDPR requirements</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Very good knowledge of SAP interface technologies</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Very Good Knowledge of SAP BTP, SAP ALM, SAP RISE model</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">General understanding of basic SAP technology, logistic, accounting &amp; reporting functions</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">General knowledge on consulting and incident management processes</li></ul>&nbsp;Requirements:&nbsp;Start: 01.10.2025Duration: 12 monthsCapacity: 5 days per weekRemote: 100%Location: Munich &amp; remote</div>

SAP Integration Consultant

<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); font-family: Arial; font-size: 11pt;">Sicherheits- und Gesundheitskoordinator Baustelle Pharma (M/W/D)&nbsp;Information zu dem Projekt: Beratung bei verschiedene Baustellen notwendig: BioDS und F5 am Standort&nbsp;Aufgaben:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Beratung der Projektteams vor Ort sowie des HSQ-Managers in Arbeitssicherheits- und Gesundheitsschutzthemen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Entwicklung, Implementierung und Überwachung von Konzepten und Richtlinien gemäß gesetzlichen Vorschriften und internen Standards</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Durchführung von Sicherheitsbegehungen und Erstellung von Gefährdungsbeurteilungen in fachlicher Zusammenarbeit mit der Projektleitung</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Analyse und Dokumentation von Unfällen sowie Entwicklung von Maßnahmen zur Unfallverhütung</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Durchführung von Schulungen und Unterweisungen in Sicherheits- und Gesundheitsschutzthemen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Vorbereitung und Durchführung von ISO-Audits (9001, 14001, 45001)</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Projektbezogene Kommunikation mit Behörden, Berufsgenossenschaften und Partnern</li></ul>&nbsp;Qualifikation:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Meister, Techniker, Ingenieur oder Absolvent der Sicherheitstechnik, Fachkraft für Arbeitssicherheit (Sifa)</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">3–5 Jahre Erfahrung im Bereich Arbeitssicherheit, vorzugsweise im Bau- oder Energiesektor</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Fundierte Kenntnisse relevanter Gesetze und Normen im Arbeitsschutz</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Sehr gute Deutsch- und gute Englischkenntnisse, weitere Sprachen von Vorteil</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Hohe Beratungskompetenz und Kommunikationsstärke</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Ausgeprägtes Durchsetzungsvermögen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Proaktive und lösungsorientierte Denkweise sowie strukturierte Arbeitsweise</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Kenntnisse von relevanten Normen wie DIN ISO 14001:2015, DIN 45001:2018, DIN ISO 50001:2018, der techn. Regelwerke VOB/B und VOB/C.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Eigenständige Durchführung von Risikoanalysen und internen Audits.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Fähigkeit zur Schulung und Beratung von Mitarbeitern</li></ul>&nbsp;Rahmendaten:&nbsp;Start: 01.11.2025Dauer: 12 MonateAuslastung: 5 Tage die WocheEinsatzort: München&nbsp;</div>

Sicherheits- und Gesundheitsschutzkoordinator Baustelle Pharma

<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); font-family: Arial; font-size: 11pt;">Technical Project Lead (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside;"><li>Lead the end-to-end process of identifying, evaluating, and conceptualizing Automated Visual Inspection (AVI) technologies for IV bag production</li><li>Translate strategic innovation goals into actionable scouting and design activities, ensuring alignment with regulatory, quality, and operational requirements</li><li>Deliver a comprehensive Concept Design package, enabling seamless transition to Basic Design and project execution phases</li><li>Act as a key interface between internal stakeholders and external technology providers to drive innovation from ideation to execution</li><li>Develop URS and TechSpecs for AVI in IV bag applications</li><li>Conduct full-scale technology scouting, including vendor landscape analysis (qualified, early adopters, PoC, roadmap)</li><li>Request and analyze budgetary quotations; perform vendor evaluations using KT-analysis</li><li>Lead feasibility studies with vendors and document outcomes</li><li>Design process layouts and develop holistic Concept Designs</li><li>Facilitate supplier feedback and refine technical and commercial proposals</li><li>Recommend preferred supplier and ensure handover to Basic Design phass</li><li>Ensure execution readiness and alignment with project timelines (3–6 months)</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside;"><li>Degree in Engineering, Life Sciences, or related technical field</li><li>10+ years of experience in pharmaceutical engineering or related industry</li><li><div style="font-family:Arial;font-size:11pt;">Capable of leading cross-functional teams and external partners</div></li><li>Expertise in AVI</li><li>Strong background in process engineering and visual inspection technologies, ideally in parenteral or IV bag manufacturing</li><li>Strong supplier management skills, including vendor assessment, contracting, and performance verification</li><li>Experience in URS/TechSpec development, vendor management, and feasibility studies</li><li>Experience in facilitating supplier engagement and feedback loops during concept and feasibility phases</li><li>Familiarity with cGMP, regulatory requirements, and pharmaceutical automation</li><li>Familiarity with AI/ML applications in visual inspection, including data requirements and algorithm validation</li><li>Hands-on approach with the ability to drive execution from scouting to concept finalization Innovation</li><li>Proven ability to scout, evaluate, and implement emerging technologies (e.g. AI in AVI)</li><li>Experience with PoC, prototype testing, and early-stage technology validation</li><li>Ability to benchmark and position AVI solutions within the broader industry landscape</li><li>Capable of leading cross-functional teams and external partners</li><li>Demonstrated experience in implementing emerging technologies into commercial manufacturing environments</li><li>Strong project management and technical writing skills</li><li>Fluent in English (written and oral)</li><li>Travel to vendor sites and internal facilities expected (up to 30%)</li></ul>&nbsp;Requirements:&nbsp;Start: asapDuration: 6 monthsCapacity: 5 days per weekLocation: Zurich, Switzerland</div>

Technical Project Lead

<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); font-family: Arial; font-size: 11pt;">Medical Information Lead (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside;"><li>As subject matter expert on the therapeutic areas and medical information best practices, the GMI Medical Information Lead is responsible for the management of complex inquiries for EMEA across global product portfolio&nbsp;</li><li>Management of medical information content in alignment with the product life-cycle and regulatory milestones and leveraging the global medical information content strategy cross-regionally</li><li>Support and training of business units and vendors on GMI processes and EMEA best practices&nbsp;</li><li>Ensure appropriate, quality and timely responses to requests for medical information in EMEA for therapeutic areas of responsibility&nbsp;</li><li>Develop or adapt available medical information content to be used globally&nbsp;</li><li>Support novel channels for dissemination of medical information&nbsp;</li><li>Support new digital technologies and systems in accordance with GMI digital strategy&nbsp;</li><li>Manage medical information providers&nbsp;</li><li>Develop and implement medical information support materials in coordination with Global Medical Teams and Medical Communications, as well as Local Medical Information teams, where appropriate&nbsp;</li><li>Ensure reporting of potential adverse events and product quality complains to appropriate teams</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0cm; margin-top: 0cm;" 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;">A medical or scientific degree is required</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;">5 years of related work 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;">4 years of experience in the biopharmaceutical industry, preferably within a matrix structure isrequired</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;">2 years of experience within medical affairs, clinical research or PV/safety roles (e.g. Medical Information, Medical Communications, Pharmacovigilance/Safety)</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;">Experience leading teams is 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;">Experience managing vendors and complex projects is required</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;">Good knowledge of medical information best practices, legal and regulatory requirements, Codes of Practice, Standard Operating Practices and guidelines</li></ul>&nbsp;Requirements:&nbsp;Start: 01.09.2025Duration: 12 monthsCapacity: 5 days per weekLocation: Zurich, Switzerland&nbsp;&nbsp;</div>

Medical Information Lead

<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); font-family: Arial; font-size: 11pt;">Oracle HCM Berater (M/W/D)&nbsp;Aufgaben:&nbsp;&nbsp;<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Beratung in der Implementierung&nbsp; von Oracle HCM, insbesondere im Modul Zeitwirtschaft (Time &amp; Labor / Oracle Fusion HCM)</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Koordination der Zusammenarbeit mit dem Implementierungspartner zur Sicherstellung der fachgerechten Umsetzung</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Übersetzung von HR Use Cases und fachlichen Anforderungen in technische Spezifikationen für die Implementierung</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Analyse und Konzeption von Lösungen für komplexe Zeitwirtschaftsszenarien mit verschiedenen Schichtmodellen und vertraglichen Regelungen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Integration bzw. Berücksichtigung von ATOSS Zeitwirtschaft und MASTEK Add-Ons im Oracle-Umfeld</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Beratung bei der Anbindung bzw. im Zusammenspiel mit Datev Payroll</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Beratung hinsichtlich Best Practices und Optimierungspotenziale im Zeitwirtschaftsbereich</li></ul>&nbsp;Qualifikation:&nbsp;<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Fundierte Erfahrung mit Oracle HCM, insbesondere im Bereich Zeitwirtschaft / Time &amp; Labor</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Projekterfahrung in der Implementierung von Zeitwirtschaftslösungen in komplexen HR-IT-Landschaften</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Ausgeprägte analytische und konzeptionelle Fähigkeiten, um Implementierungsvorschläge zu erarbeiten</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Sehr gute Deutsch- und Englischkenntnisse</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Von Vorteil:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Kenntnisse in ATOSS Zeitwirtschaft</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Erfahrung mit Datev Payroll</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Erfahrung mit MASTEK Add-Ons für Oracle HCM</li></ul></li></ul>&nbsp;&nbsp;Rahmendaten:&nbsp;Start: 01.09.2025Dauer: 2 MonateAuslastung: 3-5 TageEinsatzort: Bayern/Remote&nbsp;</div>

Oracle HCM Berater

<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); font-family: Arial; font-size: 11pt;"><div style="font-family:Arial;font-size:11pt;">Freelancer (m/w/d) – Elektrokonstruktion mit EPLAN P8 / Anlagenbau&nbsp;Für ein Projekt bei einem etablierten Industrieunternehmen suchen wir freiberufliche Unterstützung im Bereich Elektrokonstruktion, mit Schwerpunkt auf Schaltschrankplanung im Anlagenbau.<hr data-start="729" data-end="732"><h3 data-start="734" data-end="758">Projektaufgaben:</h3><ul style="list-style-position: inside;" data-start="759" data-end="1282"><li data-start="759" data-end="880">Planung und Konstruktion von elektrotechnischen Schaltungen und Schaltschränken im Rahmen komplexer technischer Anlagen</li><li data-start="881" data-end="950">Erstellung und Pflege von Stromlaufplänen mit EPLAN Electric P8</li><li data-start="951" data-end="1064">Auswahl, Auslegung und Dokumentation elektrischer Komponenten, einschließlich sicherheitsrelevanter Steuerungen</li><li data-start="1065" data-end="1182">Umsetzung kundenspezifischer Anforderungen unter Berücksichtigung geltender Normen (u. a. EMV, Maschinenrichtlinie)</li><li data-start="1183" data-end="1282">Technische Abstimmungen mit angrenzenden Abteilungen (z. B. Mechanik, Service, Projektmanagement)</li></ul><hr data-start="1284" data-end="1287"><h3 data-start="1289" data-end="1311">Anforderungen:</h3><ul style="list-style-position: inside;" data-start="1312" data-end="1759"><li data-start="1312" data-end="1443">Abgeschlossenes Studium, Technikerausbildung oder vergleichbare Qualifikation im Bereich Elektrotechnik / Automatisierungstechnik</li><li data-start="1444" data-end="1523">Mehrjährige Erfahrung im Anlagenbau sowie in der Schaltschrankplanung</li><li data-start="1524" data-end="1569">Fundierte Anwendungspraxis mit EPLAN P8</li><li data-start="1570" data-end="1641">Sicherer Umgang mit relevanten Normen und Vorschriften (z. B. EN/IEC)</li><li data-start="1642" data-end="1709">Selbstständige, strukturierte und lösungsorientierte Arbeitsweise</li><li data-start="1710" data-end="1759">Sehr gute Deutschkenntnisse in Wort und Schrift</li></ul><hr data-start="1761" data-end="1764"><h3 data-start="1766" data-end="1787">Nice to have:</h3><ul style="list-style-position: inside;" data-start="1788" data-end="1998"><li data-start="1788" data-end="1844">Kenntnisse im Bereich funktionale Sicherheit (SIL, PL)</li><li data-start="1845" data-end="1940">Projekterfahrung in regulierten Branchen (z. B. Life Science, Labortechnik, Prozessindustrie)</li><li data-start="1941" data-end="1998">Reisebereitschaft für gelegentliche Projektabstimmungen</li></ul>&nbsp;Rahmendaten:&nbsp;Start: Ab sofortDauer: 6 Monate+Auslastung: 3-5 Tage die WocheEinsatzort: Remote / Großraum München</div></div>

Elektrokonstruktion mit EPLAN P8 / Anlagenbau

<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); font-family: Arial; font-size: 11pt;">Contracts Coordinator (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside;"><li data-start="202" data-end="365">Manage Contract Management Systems (CMS)</li><li data-start="202" data-end="365">Handle vendor and site contracts from initiation to archiving, ensuring accurate filing and database updates</li><li data-start="202" data-end="365">Coordinate Contract Signatures</li><li data-start="202" data-end="365">Distribute and track contracts for internal/external signatures, promote electronic signature solutions</li><li data-start="517" data-end="648">Handle Purchase Orders &amp; Contract Distribution</li><li data-start="517" data-end="648">Process and distribute POs along with signed contracts to stakeholders</li><li data-start="650" data-end="803">Archive and Redact Contracts</li><li data-start="650" data-end="803">Scan, store, redact, and archive executed contracts in legal database, especially for audits/inspections</li><li data-start="805" data-end="958">Support Site Contracts (including CDAs)</li><li data-start="805" data-end="958">Track, scan, and distribute wet ink site contracts; handle courier logistics and database archiving</li><li data-start="960" data-end="1108">Manage HCP Contracts</li><li data-start="960" data-end="1108">Draft, review, circulate, and finalize contracts with Health Care Professionals, and ensure SAP/VMD data accuracy</li><li data-start="1110" data-end="1248">Support e-signature training/testing for CRO partners and maintain related training materials and KPIs</li><li data-start="1250" data-end="1408">Prepare documents, organize meetings, maintain department portals, and assist with travel and office needs</li><li data-start="1410" data-end="1553">Adhere to UCB SOPs, ICH/GCP, and regulatory requirements in all documentation and contract processes</li><li data-start="1555" data-end="1688">Identify process inefficiencies and participate in optimizing procedures and system usage.</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside;"><li data-start="1746" data-end="1871">Minimum 3 years’ experience in administrative, secretarial, or documentation roles (preferably in pharma/biotech/CRO).</li><li data-start="1873" data-end="1952">High attention to detail and accuracy in handling complex documentation.</li><li data-start="1954" data-end="2049">Excellent English communication skills (written and verbal); German or French is a plus.</li><li data-start="2051" data-end="2151">Strong organizational and time-management skills to manage multiple priorities independently.</li><li data-start="2153" data-end="2227">Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint).</li><li data-start="2229" data-end="2330">Understanding of clinical development regulations (FDA, EMA, ICH/GCP) and trial documentation.</li><li data-start="2332" data-end="2400">Experience with legal or paralegal documents is an advantage.</li><li data-start="2402" data-end="2495">Proactive, flexible, and able to handle shifting priorities without close supervision.</li><li data-start="2497" data-end="2581">Strong interpersonal skills to coordinate with global stakeholders and teams.</li><li data-start="2583" data-end="2684">Ability to identify and implement best practices and improve contract coordination processes.</li></ul>&nbsp;Requirements:&nbsp;Start: 01.09.2025Duration: 4 months + extension until 31.12.2026 possibleCapacity: 5 days per week (2 days onsite + 3 days in home office)Location: Monheim, Germany</div>

Contracts Coordinator

<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); font-family: Arial; font-size: 11pt;">Consultant for LIMS Evaluation and Recommendation in a Bioprocess Lab (EU) (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside;"><li>Clearly define&nbsp;the business, functional, technical, and compliance requirements of the BTRL-DSE.</li><li>Evaluate both SampleManager and IDBS Polar&nbsp;on:</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Functional capabilities aligned with lab workflows</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Total cost of ownership (licensing, implementation, ongoing support)</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Implementation complexity and timelines</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Validation and compliance requirements (GxP, 21 CFR Part 11). The solution will be used for non-GxP projects, but we consider implementing it closely following the GxP requirements (and potentially validating properly)</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">IT infrastructure, integration, and ongoing support needs in particular focusing on required human-resources as IT application support</li><li>Provide a detailed recommendation&nbsp;supported by comparative analysis, including close vendor engagement.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Gather requirements through workshops and interviews with stakeholders</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Assess existing LIMS solutions (Thermo Fisher SampleManager and IDBS Polar) regarding functionality, costs, validation, and risks</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Conduct comparative analysis and prepare an evaluation report</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Develop a recommendation for the best solution, including decision rationale</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Documentation and project based communication with stakeholders</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Experience in evaluating, implementing and managing LIMS systems, ideally in a life sciences environment</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Knowledge of regulatory standards (GxP, 21 CFR Part 11) and validation processes</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Analytical thinking, structured working style, and good communication skills</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Fluent in English; German language skills are a plus&nbsp;</li><li>Note: Freelancers must use their own equipment!&nbsp;</li></ul>&nbsp;Requirements:&nbsp;Start: 18.08.2025Duration: 12 monthsCapacity: 3-5 days per weekLocation: Remote, client is in Bayern&nbsp;</div>

Consultant  for LIMS Evaluation and Recommendation in a Bioprocess Lab (EU)

<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); font-family: Arial; font-size: 11pt;"><div style="font-family:Arial;font-size:11pt;"><div style="direction:ltr;margin-left:0in;margin-top:0in;width:6.6041in;"><div style="direction:ltr;margin-left:0in;margin-top:0in;width:6.6041in;">Production Technician (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Perform production activities related to the manufacturing of active pharmaceutical ingredients.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Ensure compliance with cGMP, BDP (Best Documentation Practices), and EHS (Environment, Health, and Safety) standards.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Conduct routine process activities, and follow predefined documentation for non-routine tasks.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Accurately report technical and organizational issues to the appropriate channels.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Take responsibility for personal training and development.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Ensure proper execution of all assigned tasks.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Promptly escalate any encountered problems or deviations.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Actively participate in continuous improvement initiatives.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Contribute to a culture of quality, safety, and operational excellence.</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Ideally BAC +2 in biotechnology, chemistry, biology, or biochemistry, or equivalent.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Good knowledge in one of the following: process support activities on a production line.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Preferred: CF diploma or certification in chemical/pharmaceutical production technology.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Prior experience in pharmaceutical, food, or chemical industries, particularly in controlled environments (cleanrooms).</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Experience in hospital-related departments (e.g., laundry, decontamination, or cleaning) is an advantage</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Solid understanding of Good Manufacturing Practice (cGMP) regulations.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Familiarity with working in a controlled atmosphere area.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Proficient in French (minimum B2 level) – both written and verbal.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Basic knowledge of MS Office (Outlook, Excel, Word) is a plus.</li></ul>&nbsp;Requirements:&nbsp;Start: asapDuration: 9 monthsCapacity: 5 days per weekLocation: Neuchatel, Switzerland&nbsp;</div></div></div></div>

Production Technician

<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); font-family: Arial; font-size: 11pt;"><div style="font-family:Arial;font-size:11pt;">Qualification Engineer (M/W/D)&nbsp;Wir suchen einen Qualification Engineer, der Qualifizierungsaktivitäten im Bereich Drug Product / Fertigwarenproduktion unterstützt. Dazu gehören sterile Abfüllanlagen, Reinräume, Gefriertrockner und verwandte Ausrüstungen in bestehenden sowie neuen Produktionsstätten.<h3 data-start="370" data-end="387">Aufgaben:</h3><ul style="list-style-position: inside;" data-start="389" data-end="734"><li data-start="389" data-end="469">Durchführung von Qualifizierungen für Anlagen und Systeme (URS, DQ/IQ/OQ/PQ)</li><li data-start="470" data-end="578">Unterstützung bei Change Control und Abweichungsmanagement (Root Cause Analysis, technische Bewertungen)</li><li data-start="579" data-end="647">Umsetzung von Prozessverbesserungen und Einführung neuer Systeme</li><li data-start="648" data-end="734">Enge Zusammenarbeit mit den Bereichen Produktion, Qualitätssicherung und Engineering</li></ul><h3 data-start="736" data-end="758">Anforderungen:</h3><ul style="list-style-position: inside;" data-start="760" data-end="1072"><li data-start="760" data-end="852">Abgeschlossenes Studium im Bereich Ingenieurwesen, Naturwissenschaften oder vergleichbar</li><li data-start="853" data-end="913">Erfahrung in der Qualifizierung pharmazeutischer Anlagen</li><li data-start="914" data-end="983">Kenntnisse der cGMP-Richtlinien und regulatorischen Anforderungen</li><li data-start="984" data-end="1072">Ausgeprägte Problemlösungsfähigkeiten sowie Erfahrung in der technischen Dokumentation</li></ul><h3 data-start="1074" data-end="1094">Rahmendaten:</h3><ul style="list-style-position: inside;" data-start="1096" data-end="1218"><li data-start="1096" data-end="1115">Start: ASAP</li><li data-start="1116" data-end="1140">Dauer: 12 Monate</li><li data-start="1141" data-end="1169">Auslastung: Vollzeit</li><li data-start="1170" data-end="1218">Einsatzort: Vor Ort (1 Tag Remote möglich)</li></ul></div></div>

Qualification Engineer

Projektleiter / Expert Produktionstransfer medizinischer Laser USA - Deutschland

<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); font-family: Arial; font-size: 11pt;">MLR Review Process Manager (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0cm; margin-top: 0cm;" 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;">Lead digital submission readiness reviews in content (medical and commercial) review process and monitor project status to ensure schedules and deadlines are being met</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;">Manage and facilitate the full content approval process for both non-promotional and promotional materials</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;">Work with internal and external stakeholders, including project owners, medical, legal and regulatory review process reviewers, agencies, and CPOs (local countries), to plan and route materials to appropriate reviewers for timely compliance 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;">Provide guidance to project owners and vendors/agencies on submission requirements</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;">Facilitate review/concept review meetings, monitor the status of system tasks and fol-low-up, update/maintain system delegations</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;">Be responsible for Readiness Checks (reviewing and ensuring materials are submission- ready)</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 final approved materials are “final approved” and appropriately documented</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;">Communicate and manage team expectations on status, volume, and prioritization.</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;">System FUSE role will be a blend of MLR Facilitator and Superuser empowering system and process solutions to be processed and solved at once</li></ul>&nbsp;&nbsp;Requirements:&nbsp;Start: 01.08.2025Duration: 12 monthsCapacity: 5 days per weekLocation: client is in Basel, job can be done 100% remote</div>

MLR Review Process 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); font-family: Arial; font-size: 11pt;">Quality Control Analyst (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside;" data-end="423" data-start="205"><li data-end="311" data-start="205">Perform QC analyses and sample collections in compliance with SOPs, cGMPs, and pharmacopoeial standards</li><li data-end="423" data-start="312">Complete documentation (forms, logbooks, results systems) per Good Manufacturing and Documentation Practices</li><li data-end="570" data-start="470">Notify supervisors of non-conforming/invalid results and initiate quality events within deadlines</li><li data-end="659" data-start="571">Proactively report planning deviations and escalate procedural deviations as required</li><li data-end="777" data-start="686">Comply with and promote EHS rules; address unsafe behaviors and open EHS events promptly</li><li data-end="863" data-start="778">Participate in maintaining a safe, compliant lab environment during all activities</li><li data-end="1010" data-start="912">Execute validation and qualification protocols for methods, systems, equipment, and consumables</li><li data-end="1100" data-start="1011">Perform recalculations, supervise external results, and reconcile controlled documents</li><li data-end="1211" data-start="1135">Ensure equipment calibration/maintenance is current and report any issues.</li><li data-end="1286" data-start="1212">Conduct GEMBAs, review alarms, and uphold 5S lab organization standards.</li><li data-end="1411" data-start="1332">Train analysts and apprentices on equipment and GMP; act as a backup trainer</li><li data-end="1492" data-start="1412">Maintain up-to-date training status (e.g., SABA) and complete modules on time.</li><li data-end="1620" data-start="1538">Act as SME for methods/equipment, resolving complex issues and supporting CAPAs</li><li data-end="1723" data-start="1621">Back up supervisor or QC lifecycle roles and contribute to risk analyses and regulatory submissions</li><li data-end="2088" data-start="1990">Manage logbooks, trend reports, and data systems (RAM, Bolton) with strong data integrity focus</li><li data-end="2312" data-start="2234">Assess result validity/conformity and escalate priority conflicts as needed.</li><li data-end="2407" data-start="2313">Support and initiate corrective and preventive actions in collaboration with lab leadership</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside;" data-end="3897" data-start="3618"><li data-end="3743" data-start="3618">Minimum CFC (Swiss Federal Certificate) in microbiology or equivalent experience in the pharmaceutical or biotech industry.</li><li data-end="3816" data-start="3744">2–5 years of experience in a cGMP lab or minimum 2 years as Analyst I.</li><li data-end="3897" data-start="3817">At least 5 years of experience in a cGMP lab or minimum 5 years as Analyst II</li><li data-end="3974" data-start="3929">Good to excellent knowledge of lab methods.</li><li data-end="4017" data-start="3975">Good understanding of cGMP requirements.</li><li data-end="4095" data-start="4018">Knowledge of Data Integrity and its application in a regulated environment.</li><li data-end="4195" data-start="4129">Comfortable with standard office and IT tools (MS Office suite).</li><li data-end="4236" data-start="4196">French and technical English required.</li><li data-end="4265" data-start="4237">English level: minimum B2</li></ul>&nbsp;Requirements:&nbsp;Start: 21.07.2025Duration: 4 monthsCapacity: 5 days per weekLocation: Neuchatel, Switzerland&nbsp;</div>

Quality Control 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); font-family: Arial; font-size: 11pt;">IT Transition Expert (M/W/D)&nbsp;Aufgaben:<ul style="list-style-position: inside;"><li data-end="152" data-start="75">Service Transition neuer Funktionen inkl. Schulung &amp; Trainingsmaterialien</li><li data-end="236" data-start="153">Aufbau &amp; Pflege einer Wissensdatenbank in Zusammenarbeit mit Training &amp; Support</li><li data-end="299" data-start="237">Erstellung nachhaltiger System- und Prozessdokumentationen</li><li data-end="379" data-start="300">Optimierung &amp; Weiterentwicklung von IT-Prozessen mit Stakeholder-Abstimmung</li><li data-end="450" data-start="380">Steuerung externer Dienstleister zur Einhaltung von Service Levels</li><li data-end="500" data-start="451">Projektsupport gemäß Vorgaben des Fachbereichs</li></ul>&nbsp;Qualifikation:&nbsp;<ul style="list-style-position: inside;"><li data-end="124" data-start="65">Projekt- und Transitionserfahrung im digitalen Umfeld, idealerweise in Pharma oder Life Sciences</li><li data-end="124" data-start="65">Kenntnisse in ITIL-Prozessen, ServiceNow, Jira, Confluence, SharePoint; Erfahrung mit SAP HANA und KI ist ein Plus</li><li data-end="171" data-start="125">Analytisches, lösungsorientiertes Arbeiten und starke Kommunikationsfähigkeiten</li><li data-end="232" data-start="172">Hohe Serviceorientierung, Belastbarkeit und Flexibilität</li><li data-end="294" data-start="233">Schnittstellenübergreifende Zusammenarbeit &amp; Dienstleistersteuerung</li><li data-end="338" data-start="295">Sehr gute Deutsch- und Englischkenntnisse<p style="color: rgb(0, 0, 0); font-family: &quot; undefined: TimesNewRoman&quot; font-size: medium; font-style: normal; font-weight: 400; letter-spacing: normal; margin: 0; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;">&nbsp;</li></ul>&nbsp;Rahmendaten:&nbsp;Start: 11.08.2025Dauer: bis Jahresende mit Option auf VerlängerungAuslastung: 4-5 Tage die WocheEinsatzort: Hamburg &amp; remote (Wohnort HH ist Must)&nbsp;</div>

IT Transition Expert

<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); font-family: Arial; font-size: 11pt;">Quality Engineer (M/W/D)&nbsp;Tasks:&nbsp;<ul style="list-style-position: inside; padding-left: 48px;"><li>Validation of CNC Milling machines</li><li>Validate a defined article group across different processes</li><li>Prepare complete documentation, including VP, Study (if necessary), IQ, TMV (if necessary), OQ, PQ, VR</li><li>Monitor and ensure the quality of the entire article group from VP preparation through implementation into the QM</li><li>Execute all relevant validation activities in accordance with SOPs</li><li>Specify and qualify test equipment, perform process and equipment validation</li><li style="line-height:115%;margin-bottom:0cm;margin-right:0cm;margin-top:0cm;">Identify and implement improvement measures&nbsp;</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside; padding-left: 48px;"><li>Several years of experience in a regulated, high-volume industrial production environment</li><li>Strong background in ISO 13485, ISO 9001, FDA regulations</li><li>Medical technology experience</li><li>Ability to develop solutions and drive improvement initiatives independently</li><li>Excellent written and spoken English and German skills</li></ul>&nbsp;Details:Start:&nbsp;Asap, 1st of August 2025Duration:&nbsp;13 motnhsHours per week:&nbsp;full-time (40 hours / week)Location:&nbsp;50% onsite in North Germany / 50% remote</div>

Quality 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); font-family: Arial; font-size: 11pt;">PV Manager (M/W/D)&nbsp;Aufgaben:&nbsp;<ul style="list-style-position: inside; padding-left: 48px;"><li>Erfassung, Bewertung und medizinische Codierung von ICSRs (spontan, Studien, Literatur etc.)</li><li>Erstellung und QC von CIOMS-Fällen</li><li>SAE Handling inkl. Follow-up</li><li>Durchführung und Dokumentation von Signaldetektion</li><li>Bewertung neuer Sicherheitsinformationen</li><li>Erstellung, Review und/oder Management regulatorischer PV-Dokumente (Periodics)</li><li>Nachbereitung von PV-Audits und Inspektionen</li><li>CAPA-Management</li><li>Systematische Literaturrecherche und -auswertung</li><li>Relevanzprüfung von Publikationen für PV-Zwecke</li><li>Arbeit mit Safety-Datenbanken (Eudravigilance)</li></ul>&nbsp;Qualifikation:<ul style="list-style-position: inside; padding-left: 48px;"><li>Mehrjährige Erfahrung in allen Bereichen der Pharmakovigilanz</li><li>Sehr gute Kenntnisse der einschlägigen regulatorischen Anforderungen (GVP, ICH, EU-Vorgaben)</li><li>Erfahrung mit Eudravigilance</li><li>Erfahrung im Umgang mit Behörden und bei Audits/Inspektionen</li><li>Selbständige, strukturierte Arbeitsweise mit Hands-on-Mentalität</li><li>Sehr gute Deutsch- und Englischkenntnisse</li></ul>&nbsp;Rahmendaten:Start:&nbsp;Asap, spätestens Juli 2025Dauer:&nbsp;3-6 MonateWochenstunden:&nbsp;8-12 Stunen pro WocheOrt:&nbsp;Remote + Hamburg (Gelegentlich vor Ort)</div>

PV 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); font-family: Arial; font-size: 11pt;">Inhouse Solution Architect SAP (M/W/D)&nbsp;Aufgaben:<ul style="list-style-position: inside;" data-end="1349" data-start="203"><li data-end="359" data-start="203">Konzeption und Umsetzung von SAP S/4HANA-Lösungen unter Einsatz neuester Technologien wie ABAP 7.4+, Cloud ABAP, RAP, HANA, SAPUI5 sowie IoT-Anwendungen</li><li data-end="477" data-start="360">Weiterentwicklung und Anpassung von SAP-Modulen zur effizienten Gestaltung und Optimierung von Geschäftsprozessen</li><li data-end="563" data-start="478">Beratung in den Bereichen Systemarchitektur, Lösungsdesign und SAP Best Practices</li><li data-end="688" data-start="564">Sicherstellung der Ausrichtung der Geschäftsprozesse an der IT-Strategie und den übergreifenden Architekturanforderungen</li><li data-end="769" data-start="689">Unterstützung bei der Erstellung von Business Cases zur Entscheidungsfindung</li><li data-end="840" data-start="770">Ausarbeitung technischer Spezifikationen sowie deren Dokumentation</li><li data-end="912" data-start="841">Steuerung und Koordination externer Dienstleister im Projektkontext</li><li data-end="1014" data-start="913">Verantwortung für Systemimplementierungen inklusive Testdurchführung, Change- und Freigabeplanung</li><li data-end="1095" data-start="1015">Mitwirkung bei der Entwicklung von Schulungsunterlagen und Know-how-Transfer</li><li data-end="1174" data-start="1096">Erstellung und Pflege technischer und fachlicher Anwendungsdokumentationen</li><li data-end="1271" data-start="1175">Übernahme von Projektverantwortung sowie eigenständige Bearbeitung projektähnlicher Aufgaben</li><li data-end="1308" data-start="1272">Übernahme des 2nd Level Supports</li><li data-end="1349" data-start="1309">Schulung und Betreuung von Key-Usern</li></ul><hr data-end="1354" data-start="1351"><h3 data-end="1378" data-start="1356">Qualifikation:</h3><ul style="list-style-position: inside;" data-end="2166" data-start="1380"><li data-end="1490" data-start="1380">Abgeschlossenes Studium in Wirtschaftsinformatik, Betriebswirtschaft oder eine vergleichbare Qualifikation</li><li data-end="1632" data-start="1491">Mehrjährige, fundierte Praxiserfahrung in mindestens einer SAP-Technologie wie der Business Technology Platform, ABAP, Fiori oder S/4HANA</li><li data-end="1697" data-start="1633">Ausgeprägte technische Kenntnisse in SAP ABAP und JavaScript</li><li data-end="1740" data-start="1698">Umfangreiche Erfahrung mit SAP S/4HANA</li><li data-end="1810" data-start="1741">Wünschenswert sind Kenntnisse in komplexen Intercompany-Prozessen</li><li data-end="1942" data-start="1811">Strukturierte, analytische und selbstständige Arbeitsweise gepaart mit einem serviceorientierten, agilen und proaktiven Mindset</li><li data-end="2028" data-start="1943">Nachgewiesene Erfahrung in der Arbeit in Projekten, idealerweise in agilen Setups</li><li data-end="2100" data-start="2029">Teamfähigkeit, Eigeninitiative und ausgeprägte Kommunikationsstärke</li><li data-end="2166" data-start="2101">Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift</li></ul>&nbsp;Rahmendaten:&nbsp;Start: asapDauer: FestanstellungAuslastung: 5 Tage die WocheEinsatzort: München (3 Tage vor Ort) &amp; Remote (2 Tage aus HO)&nbsp;&nbsp;&nbsp;</div>

Inhouse Solution Architect SAP

<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); font-family: Segoe UI; font-size: 11pt;">Supply Chain System Adoption Lead (M/F/D)&nbsp;Tasks:<ul style="list-style-position: inside; padding-left: 24px;"><li>Conduct change assessments and surveys to gauge system adoption readiness.</li><li>Create and execute training plans to enhance user engagement and knowledge.</li><li>Monitor system usage and generate engagement plans to increase adoption.</li><li>Identify barriers to adoption and recommend corrective actions.</li><li>Stakeholder Mapping &amp; Engagement: Identify key stakeholders, map their influence and involvement, and create engagement strategies to secure buy-in and alignment throughout the project lifecycle.</li><li>Impact Analysis: Assess how changes to the planning system will affect various business units, processes, and roles. Create mitigation strategies for potential resistance.</li><li>Communication Planning: Develop a structured communication plan to inform stakeholders of key milestones, changes, and benefits, ensuring clarity and minimizing disruptions.</li><li>Readiness Assessments: Regularly assess organizational readiness for new processes and system updates. Address gaps through targeted interventions.</li><li>Behavioral Reinforcement Plans: Design initiatives to reinforce desired behaviors post-implementation, including coaching, mentoring, and feedback loops.</li><li data-start="0" data-end="174">Design, deliver, and maintain comprehensive training programs and materials (e.g., guides, manuals, playbooks) to support continuous learning and system user development.</li><li data-start="175" data-end="325" data-is-last-node>Oversee and align functional learning in planning with organizational goals, ensuring timely updates and communication of new processes and modules.</li><li>Establish metrics (KPIs) to monitor system usage, training effectiveness, and process adherence.</li><li>Conduct regular workshops and refresher training sessions to maintain skill levels and address evolving business needs</li></ul>&nbsp;Qualification:<ul style="list-style-position: inside;"><li>Minimum 5 years of experience in technology adoption, system implementation, supply chain management and/or change management.</li><li>Bachelor’s degree in management, Business Administration, or a related field.</li><li>Change Management certification strongly preferred</li><li>Experience in leading organizational change and transformation in supply chain organizations.&nbsp;</li><li>Proven experience with system adoption and large-scale training programs.</li><li>Strong understanding of planning tools and processes.</li><li>Excellent communication and organizational skills.</li><li>Proficiency in documentation management.</li><li>Proven experience in supply chain planning and data analysis.</li><li>Strong project management skills.</li><li>Excellent communication and training skills.</li><li>Proven knowledge and experience in PowerBI, Advance analytics tools</li></ul>&nbsp;Requirements:&nbsp;Start: 01.10.2025Duration: 12 monthsCapacity: 5 days per weekLocation: Baar Switzerland&nbsp;&nbsp;</div>

Supply Chain System Adoption Lead

<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); font-family: Segoe UI; font-size: 11pt;"><div style="font-family:Segoe UI;font-size:11pt;"><div style="direction:ltr;margin-left:0in;margin-top:0in;width:7.3208in;"><div style="direction:ltr;margin-left:0in;margin-top:0in;width:7.3208in;">Interim MSL (Mitteldeutschland) (M/W/D)&nbsp;&nbsp;Aufgaben:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; padding-inline-start: 40px; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Identifikation, Selektion, Charakterisierung und kontinuierliche Betreuung von KOLs im jeweiligen Indikationsgebiet. Erste Ansprechperson der KOLs für den wissenschaftli­chen Dialog.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Recherche von Versorgungsstrukturen und Leitlinien in Vorbereitung geplanter Produkt­neueinführungen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Intensive Literaturrecherche sowie Kongressbesuche mit an­schließender Berichterstat­tung, Identifikation und laufende Beobachtung von Konkurrenzprodukten&nbsp;</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">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)</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Mitarbeit an nationalen und regiona­len Expertentreffen und Referententrainings</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Regionale Umsetzung von klinischen Projekten (IITs, NIS, Registerstudien)</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Konzeption, Budgetierung und Durchführung regionaler wissenschaftlicher Projekte&nbsp;</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Teilnahme an internationalen, nationalen und regionalen Kongressen und Veranstaltungen&nbsp;</li></ul>&nbsp;Qualifikation:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; padding-inline-start: 40px; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Mehrjährige Tätigkeit als MSL (nice to have) oder in vergleichbaren Rollen (</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Abgeschlossenes Studium der Medizin, Naturwissenschaften oder Pharmazie, vorzugswei­se mit Promotion&nbsp;</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Berufliche Erfahrung in den Indikationen Intensivmedizin/Kardiologie und im Klinikgeschäft vorzugswei­se Erfahrungen mit Sepsis, Betablockern, Car-T-Cell Therapie</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Ausgeprägte Fähigkeit zur zügigen, eigenständigen Einarbeitung in neue Indikationen und wissenschaftliche Inhalte (z. B. durch Publikationsanalyse).</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Fundierte Kenntnisse von AMG, HWG und der einschlägigen Compliance-Kodizes&nbsp;</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Profunde Kenntnisse gängiger IT-Anwendungen (MS Office), insbes. Power Point&nbsp;</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Sehr gute Englischkenntnisse in Wort und Schrift&nbsp;</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Reisebereitschaft inkl. externer Übernachtungen (Home-Office-basiert im Gebiet)</li></ul>&nbsp;Rahmendaten:&nbsp;&nbsp;Start: ASAP&nbsp;Dauer: PermAuslastung: 5 Tage die Woche&nbsp;Einsatzort: Mitteldeutschland (Düsseldorf-Dresden)&nbsp;</div></div></div></div>

MSL (Mitteldeutschland)

<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); font-family: Segoe UI; font-size: 11pt;"><div style="font-family:Segoe UI;font-size:11pt;"><div style="direction:ltr;margin-left:0in;margin-top:0in;width:6.1055in;"><div style="direction:ltr;margin-left:0in;margin-top:0in;width:6.1055in;">Medical Science Liaison (M/W/D)&nbsp;Aufgaben:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; padding-inline-start: 40px; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Medizinisch-wissenschaftlicher Experte im Bereich der Atemwegserkrankungen innerhalb eines cross-funktionalen Brand-Teams</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Entwicklung und Umsetzung medizinischer Strategien im Einklang mit dem Brand-Plan, basierend auf erhobenen Kunden-Insights</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Aufbau und Pflege von Peer-to-Peer-Beziehungen mit externen Experten (70–80 % Außendienstanteil)</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Unterstützung von Zulassungs-, Market-Access- und Marketingteams bei medizinisch-wissenschaftlichen Fragestellungen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Unterstützung klinischer Studienprogramme (lokal, regional, global) sowie extern initiierter Studienprojekte</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Mitwirkung bei der Generierung von Real-World Evidence in der jeweiligen Therapieindikation</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Medizinische Unterstützung vertrieblicher Maßnahmen und deren Materialien</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Konzeption und Durchführung medizinischer Schulungen für Außendienst und interne Mitarbeitende</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Organisation und Umsetzung wissenschaftlicher Veranstaltungen (z. B. Symposien, Advisory Boards)</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Teilnahme an nationalen/internationalen Kongressen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Unterstützung medizinischer Anfragen (Medical Information, Patient Safety)</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Einhaltung regulatorischer und unternehmensinterner Compliance-Vorgaben</li></ul>&nbsp;Qualifikation:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; margin-top: 0in; padding-inline-start: 40px; unicode-bidi: embed;" type="disc"><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Studium der Medizin, Pharmazie oder Naturwissenschaften</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Fundierte medizinische Kenntnisse im Bereich Atemwegserkrankungen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Erfahrung in der pharmazeutischen Industrie, idealerweise als MSL oder im Bereich Medical Affairs</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Kenntnisse des österreichischen Arzneimittelgesetzes sowie des Pharmig-Kodex</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Fähigkeit zur Analyse und zielgruppengerechten Aufbereitung wissenschaftlicher Daten</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Ausgezeichnete Präsentations- und Kommunikationsfähigkeiten</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Hohe Eigenmotivation, Selbstorganisation und Koordinationsgeschick</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Sicherer Umgang mit MS Office</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Führerschein Klasse B sowie Reisebereitschaft innerhalb Österreichs</li></ul>&nbsp;Rahmendaten:&nbsp;Start: asap / Juni&nbsp;Dauer: unbefristetAuslastung: VollzeitEinsatzort: West-Österreich&nbsp;</div></div></div></div>

MSL -  Respiratory & Immunology  - West AT

<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); font-family: Segoe UI; font-size: 11pt;">LIS-Applikationsspezialist (M/W/D)&nbsp;Aufgaben:&nbsp;<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; 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;">Aktive Mitarbeit an IT-Projekten bei der Einführung neuer Labor Informationssysteme (LIS).</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Konfigurierung und Testen von Schnittstellen zwischen LIS.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Stammdaten exportieren/abgleichen zwischen LIS und vorhandenen IT Systemen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Workflow im Labor einrichtigen, konfigurieren und testen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">IT-Betreuung von LIS (z. B. MOLIS, OPUS::L, OSM, MCS Promed.open, MELOS, Swisslab, LX, Labsolution, Medat).</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Bearbeitung von Supportanfragen und ggf. Koordination relevanter IT-Dienstleister.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Koordination, Prüfung und Dokumentation von Systemupdates.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Testung neuer Softwarepakete und Installationsroutinen im Laboralltag.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Begleitung von IT-Projekten und größeren Change-Prozessen, inklusive teamübergreifender Koordination und Einbindung externer Dienstleister.</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Teilnahme an der Rufbereitschaft zur Sicherstellung des IT-Betriebs.</li></ul>&nbsp;&nbsp;Qualifikation:<ul style="list-style-position: inside; list-style-type: disc; margin-bottom: 0in; 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;">Erfahrung/Ausbildung als Laborant (min. 3 Jahre, präferiert 5 Jahre) mit hoher IT-Affinität und erster Erfahrung mit LISoder</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">IT-Studium für Anwendungsentwicklung und erste Erfahrung im Labor für Humanmedizin/Medizintechnik</li><li><div style="font-family:Segoe UI;font-size:11pt;">Alternativ eine erfolgreich abgeschlossene&nbsp;Berufsausbildung zum Medizin-/ Fachinformatiker (m/w/d) für Anwendungsentwicklung&nbsp;oder vergleichbar&nbsp;</div></li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Erfahrung im Umgang mit&nbsp;LIS&nbsp;oder ähnlichen&nbsp;medizinischen Applikationen</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Erfahrung mit LIS Systeme z.b. MOLIS, OPUS::L, OSM, MCS Promed.open, MELOS, Swisslab, LX, Labsolution, Medat</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Schnelle&nbsp;Auffassungsgabe,&nbsp;Lernbereitschaft&nbsp;und&nbsp;Serviceorientierung</li><li style="margin-bottom:0;margin-top:0;vertical-align:middle;">Bereitschaft zu&nbsp;gelegentlichen Dienstreisen&nbsp;innerhalb Süd-Deutschlands</li></ul>&nbsp;&nbsp;Rahmendaten:&nbsp;Start:&nbsp; Ab SofortDauer: 18 MonateAuslastung: 3-5 TageEinsatzort: Onsite/Remote</div>

LIS-Applikationsspezialist (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;"><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>

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