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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.

Apply to join our team.

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.

Are you interested in this project?

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Einer unserer Medizintechnik-Kunden in Baden-Württemberg sucht aktuell freiberufliche Beratung als: 
&nbsp; 
Experte im Bereich Ertragsteuern (M/W/D) 
&nbsp; 
Aufgaben: 
&nbsp;

<ul>
	<li style="margin-left:32px;list-style-position:inside">Projekt- und Beratungsleistung bei der Vorbereitung der Ertragsteuererklärungen</li>
	<li style="margin-left:32px;list-style-position:inside">Projekt- und Beratungsleistung im Bereich Quellensteuern / § 50a Anmeldungen</li>
	<li style="margin-left:32px;list-style-position:inside">Beratungsleistung bei der Beantwortung laufender Anfragen (z.B. zu Sachzuwendungen, Spenden, etc.)</li>
	<li style="margin-left:32px;list-style-position:inside">Beratungsleistung bei der Beantwortung von Anfragen der laufenden Betriebsprüfung</li>
	<li style="margin-left:32px;list-style-position:inside">Beratungsleistung bei der Prüfung von Bescheiden (z.B. Körperschaftsteuer-, Gewerbesteuer- und Zinsbescheide)</li>
</ul>

<div>&nbsp;&nbsp; 
Qualifikation: 
&nbsp;

<ul>
	<li style="margin-left:31px;list-style-position:inside">Mehrjährige Erfahrung im Bereich Ertragsteuer, z.B. aus der Tätigkeit in einer Steuerkanzlei bzw. Steuerabteilung</li>
	<li style="margin-left:31px;list-style-position:inside">Erfahrung im Industriekundenumfeld</li>
	<li style="margin-left:31px;list-style-position:inside">Gute Englischkenntnisse wünschenswert</li>
</ul>
</div>

 
Rahmendaten: 
Start: ASAP 
Dauer: ca. 4 Monate 
Auslastung: ca. 4-5 Tage / Woche 
Einsatzort: Hauptsächlich Remote</div>

Experte im Bereich Ertragsteuer (m/w/d)

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Graduate Trainee Oncology (M/W/D)

&nbsp;

Tasks:

&nbsp;

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Co-develops and realizes marketing materials to support the sales team, starting from its conceptualization or based on materials developed by the global team or other countries, including the integration of the local team’s feedbacks and the interaction with graphic agencies. </li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Timely reviews promotional materials within the review process to ensure marketing materials and projects are cleared for promotional use and secures final production</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Co-develops and executes multichannel customer engagement projects and digital brand strategies </li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Collaborates proactively to the strategy and tactical plan development</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">In order to develop and implement projects, collaborates and liaises with Medical, Regulatory, Market Access, Commercial Operations, Legal, Public Affairs and Finance </li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Supports the Senior Product Manager and Business Unit Director in preparation of trainings, meetings, market research, sales analysis, etc.</li>
</ul>

&nbsp;

Qualification:

&nbsp;

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Scientific background (master in science, PhD, etc.) </li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Familiarity with marketing fundamentals, strategy, sales and commercial policies and practices</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Therapeutic Area knowledge (oncology) would be an asset</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Young professionals are welcomed</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Fluent in German and English (both orally and written), French an asset</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Project management skills in a matrix/cross-functional work environment </li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Strong interpersonal skills with ability to listen, implement various feedbacks and learn fast</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Strong organizational skills, with ability to follow assignments through to completion </li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Strong analytical &amp; strategic skills </li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Advanced multichannel and digital project management skills </li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Strong communications skills with an ability to efficiently and productively communicate both orally and in writing </li>
</ul>

&nbsp;

&nbsp;

Requirements:&nbsp;

Start: 01.04.2023

Duration: 6 months + extension for another 6 months

Capacity: 5 days per week

Location: Zug

&nbsp;</div>

Graduate Trainee Marketing Oncology

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">Project Manager API CDMO (M/F/D)
&nbsp;
Tasks:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="margin-left:8px;list-style-position:inside">Consulting in the pharmaceutical industry with the goal of establishing a Contract Development and Manufacturing Organization</li><li style="list-style-position:inside">Consulting in project management for individual CDMO processes</li><li style="list-style-position:inside">Establish SOP landscape for CDMO business and advise on CDMO requirements</li><li style="list-style-position:inside">Establish communication strategies (between internal interfaces and externally)</li><li style="list-style-position:inside">Technical details, consulting on quality assurance processes and process optimization</li></ul>
&nbsp;
Qualification:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="margin-left:8px;list-style-position:inside">Master’s degree or PhD in chemistry, biochemistry, pharmaceutical science or similar</li><li style="margin-left:8px;list-style-position:inside">Good understanding of small molecule API manufacturing incl. applicable quality and regulatory standards for drug substance (cGMP, ICH, CMC)</li><li style="margin-left:8px;list-style-position:inside">5+ years of project management experience in the pharmaceutical industry in the area of drug substance / drug product development and manufacturing</li><li style="margin-left:8px;list-style-position:inside">Experience working with clients on customer projects or in management of CMOs</li><li style="margin-left:8px;list-style-position:inside">Project management certification (PMI or similar) preferred</li><li style="margin-left:8px;list-style-position:inside">Excellent organization, communication and decision-making skills, knows how to motivate other and&nbsp;drive toward desired results&nbsp;</li><li style="margin-left:8px;list-style-position:inside">Must have: English business fluent, Nice to have: German</li></ul>
&nbsp;
Requirements:&nbsp;
Start: asap, latest 30.01.2023
Duration: 6 months
Capacity: 5 days per week,&nbsp;remote and onsite
Location: Greater Area of Frankfurt am Main
&nbsp;</div>

Project Manager  CDMO

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Kunden in Bayern sucht aktuell freiberufliche Beratung als: 
&nbsp; 
Interim Finanzbuchhalter (M/W/D) 
&nbsp; 
Aufgaben: 
&nbsp;

<ul>
	<li style="margin-bottom:3px;list-style-position:inside">Projekt- und Beratungsleistung im Bereich Debitoren- / Kreditorenbuchhaltung</li>
	<li style="margin-bottom:3px;list-style-position:inside">Projekt- und Beratungsleistung bei der Kontenabstimmung</li>
	<li style="margin-bottom:3px;list-style-position:inside">Projekt- und Beratungsleistung bei der Rechnungsstellung und -prüfung</li>
	<li style="margin-bottom:3px;list-style-position:inside">Projekt- und Beratungsleistung bei der Überwachung von Zahlungsverkehr und Mahnwesen</li>
</ul>

<div> 
Qualifikation: 
&nbsp;

<ul>
	<li style="margin-left:8px;list-style-position:inside">Berufserfahrung als Finanzbuchhalter*in</li>
	<li style="margin-left:8px;list-style-position:inside">Kenntnisse in einer SAP-Umgebung (Business by Design)</li>
</ul>
</div>

 
Rahmendaten: 
Start: ASAP 
Dauer: ca. 6 Monate 
Auslastung: mind. 3-4 Tage / Woche &nbsp; 
Einsatzort: Vor Ort &amp; Remote 
</div>

Interim Finanzbuchhalter (M/W/D)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Kunden in Bayern sucht aktuell freiberufliche Beratung als: 
&nbsp; 
Interim Excel Expert (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li style="list-style-position:inside;margin-left:8px;">Projekt- und Beratungsleistung beim Datenexport aus SAP-Umgebung</li>
	<li style="margin-left:8px;list-style-position:inside">Projekt- und Beratungsleistung bei der Verwaltung von Excel Reports</li>
	<li style="margin-left:8px;list-style-position:inside">Projekt- und Beratungsleistung beim Erstellen von Excel Tabellen</li>
	<li style="margin-left:8px;list-style-position:inside">Schnittstellenmanagement mit den Abteilungen Finance &amp; Legal</li>
</ul>

<div>&nbsp;&nbsp; 
Qualifikation:

<ul>
	<li style="list-style-position:inside;margin-left:8px;">Fundierte Excel Kenntnisse (Pivot-Tabellen, S-Verweise etc.)</li>
	<li style="margin-left:8px;list-style-position:inside">Erfahrung in SAP-Umgebung (Business by Design) </li>
</ul>
</div>

 
Rahmendaten: 
Start: ASAP 
Dauer: 1-2 Monate 
Auslastung: mind. 3 Tage / Woche 
Einsatzort: Remote 
</div>

Interim Excel Expert (M/W/D)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">Safety Project Manager (M/F/D) &nbsp; Tasks: Key responsibilities of the Safety Project Manager include but not limited to:
<ul><li style="list-style-position:inside">Project Management of all Pharmacovigilance activities include but not limited to: 
<ul style="list-style-type:circle"><li style="list-style-position:inside">Activity Planning, Defining Scope, Developing Schedules and Time Estimations</li><li style="list-style-position:inside">Managing Risks and Issues, Risk Analysis</li></ul></li><li style="list-style-position:inside">Provide input in Global PSR and Risk Management planning for designated products in partnership with the GPS and other stakeholders, e.g. Global Regulatory Affairs, as appropriate.</li><li style="list-style-position:inside">Tracking and oversight of safety commitments and quality issues from preliminary and final health authority assessments reports, as well as commitments to Marketing Authorization, if applicable</li><li style="list-style-position:inside">Operational support for various PV activities, as needed, include but not limited to:<ul style="list-style-type:circle"><li style="list-style-position:inside">Signal Management</li><li style="list-style-position:inside">Management of Risk Management Plans</li><li style="list-style-position:inside">Assistance to Benefit-Risk Management</li></ul></li><li style="list-style-position:inside">Prepare and coordinate safety activities throughout the process lifecycle for various periodic safety reports (PSR):<ul style="list-style-type:circle"><li style="list-style-position:inside">Periodic Benefit Risk Evaluation Report (PBRER), including local forms and addenda</li><li style="list-style-position:inside">Periodic Safety Update Report (PSUR)</li><li style="list-style-position:inside">Addendum for Clinical Overview for Renewal (ACO)</li><li style="list-style-position:inside">Periodic Adverse Drug Experience Report (PADER)</li><li style="list-style-position:inside">Periodic SUSAR Report and Line Listings (pSUSAR)</li><li style="list-style-position:inside">Development Update Safety Report (DSUR)</li></ul></li><li style="list-style-position:inside">Supports the maintenance of the PSR and RMP data and modules within the PV IT Tool (Orbit)</li><li style="list-style-position:inside">Prepare distribution of safety reports to the recipients as per processes, timelines, and regulatory requirements</li></ul>
<div> Qualification:
<ul><li style="list-style-position:inside">Medical or science degree</li><li style="list-style-position:inside">Fluent in written and spoken English</li><li style="list-style-position:inside">Minimum 3 years relevant drug safety and/or pharmacovigilance experience</li><li style="list-style-position:inside">Minimum 3 years of experience in Project Management / Safety Project Management</li><li style="list-style-position:inside">Good knowledge of product development process</li><li style="list-style-position:inside">Proven experience with post-marketing safety reports (PBRER, PSUR, PADER, Line Listings, ACO for Renewal). Specifies personal skills and competencies required</li></ul></div>
&nbsp; Requirements:&nbsp; Start: 20.02.2023, latest 06.03.2023 Duration: until 29.03.02024 Capacity: 5 days per week Location: remote (occasionally onsite in Darmstadt)</div>

Safety Project Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Medical Research Operations (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">The Manager, MRO provides operational expertise in and oversight of the execution of post-drug approval research.&nbsp; This position supports the generation of post-approval data and medical evidence in the disease areas that Biogen addresses. The role is part of the Worldwide Medical Operations &amp; Effectiveness function within Worldwide Medical Affairs</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">The work is collaborative and is performed in conjunction with medical teams in both the global headquarters and at local affiliates</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">In this role, the successful candidate will act as an operational partner in driving data generation program execution. Working across late-stage development and marketed products, the incumbent will manage the operations for Phase 4 studies, patient registries, outcomes research, and real-world evidence programs</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Activities include study planning, start-up, vendor management, site management, tracking and reporting</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Support all project management activities for data generation projects as assigned</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Operationalize data generation projects in close collaboration with the Program Lead: &nbsp;Review committee coordination, contracting, study management team formation, publication support, filing, milestones and budget</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Provide regular updates to internal clinical trial management system for departmental projects, and compile reports from the system </li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Support the Associate Director Medical Research Operations Study Management with tracking and update of the medical dashboard </li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Act as a key point of contact between Medical Research Operations group and the external research stakeholders and partners</li>
</ul>

<div style="font-family:&quot;Open Sans&quot;,sans-serif; font-size:15px; line-height:normal; margin-bottom:0cm; margin-left:0cm; margin-right:0cm; margin-top:0cm">&nbsp;</div>

<div style="font-family:&quot;Open Sans&quot;,sans-serif; font-size:15px; line-height:normal; margin-bottom:0cm; margin-left:0cm; margin-right:0cm; margin-top:0cm">&nbsp;</div>

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Minimum of a Bachelor’s degree in a health-related field with clinical research experience</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Minimum of 7+ years of clinical research experience with minimum of 5+ years of CRO/Sponsor Project Management. </li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Strong Project Management skills including risk assessment and contingency planning</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">High level of customer orientation, awareness and focus</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Strong team leadership skills</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Preference for experience with late phase, post-market, and observational clinical research</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Neuroscience or rare disease experience preferred</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Must have: Business fluent English + Strong written and verbal communication skills.</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: February 2023

Duration: until 16.06.2023

Capacity: 5 days per week

Location: Solothurn, Switzerland

&nbsp;
</div>

Medical Research Operations

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Interim Teamlead Kongresse (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Fachliche Beratung als Interim Teamleitung im Bereich Kongresse</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Planung, Durchführung und Nachbereitung von nationalen und internationalen Kongressen</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Abstimmung mit internen und externen Partnern unter Beachtung der Compliance Vorschriften</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Koordination aller Prozesse in enger Abstimmung mit dem Team</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Management von externen Dienstleistern</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Erstellung von Reports und Präsentation</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Weiterentwicklung des Teams</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal;">Klare Spezialisierung im Bereich Eventmanagement, sowie Projekterfahrung im Bereich Kongress</li>
	<li style="margin: 0cm; line-height: normal;">Fachliche Führungserfahrung&nbsp;</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Freude an der Gestaltung von Veranstaltungen (national und international)</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Durchsetzungsfähig, Kommunikationsstark und Verhandlungsstärke</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Sehr gute Deutsch und Englischkenntnisse</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: Asap

Dauer: 6 Monate

Auslastung: 5 Tage die Woche

Einsatzort: Remote &amp; vor Ort (Bayern)</div>

Interim Teamlead Kongresse

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Business Project Manager (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="box-sizing: border-box;">Implementation and roll-out of modular content systems (and tehir related trainings)</li>
	<li style="box-sizing: border-box;">Independent project co-management (business-side) of roll-out of modular content systems and trainings</li>
	<li style="box-sizing: border-box;">Autonomous full project management of pan-European market research project</li>
	<li style="box-sizing: border-box;">Liaising with external parties and vendors</li>
	<li style="box-sizing: border-box;">Managing meeting schedule, agendas and keeping records of actions and deliverables</li>
	<li style="box-sizing: border-box;">Backward planning and overall project plan</li>
	<li style="box-sizing: border-box;">Delivering updates to senior leadership on a regular basis and stakeholder management</li>
	<li style="box-sizing: border-box;">Independent keeping track and organizing project documentation, deliverables, requirements, and business needs</li>
	<li style="box-sizing: border-box;">Developing and delivering user trainings with relevant third parties as part of the implementation plan</li>
	<li style="box-sizing: border-box;">Autonomous monitoring performance and quality delivery through user acceptance testing, feedback collection, and surveys</li>
	<li style="box-sizing: border-box;">Working alongside an agile coach to implement agile working methodology into projects</li>
	<li style="box-sizing: border-box;">Independent managing activity backlog and escalating issues for decision-making</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="box-sizing: border-box;">Proven experience as a project manager in the pharmaceutical industry</li>
	<li style="box-sizing: border-box;">Strong project management skills, including experience with agile methodologies</li>
	<li style="box-sizing: border-box;">Strong knowledge of project management tools and software&nbsp;</li>
	<li style="box-sizing: border-box;">Project experience working with external vendors and partners</li>
	<li style="box-sizing: border-box;">Project experience in developing and delivering user trainings</li>
	<li style="box-sizing: border-box;">English spoken and written necessary</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: 20.02.2023, latest 06.03.2023

Duration: until 20.08.2023

Capacity: 3 days per week,&nbsp;<strong style="-webkit-text-stroke-width:0px; background-color:#ffffff; box-sizing:border-box; color:#333333; font-family:&quot;Open Sans&quot;,sans-serif; font-size:14px; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:700; 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">Remote work&nbsp;<span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#333333; 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">possible, onsite would be preferred

Location: remote &amp; Munich

&nbsp;
</div>

Business Project Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
SAP Customer Services Expert (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="list-style-position:inside">Projekt im SAP Modul Customer Service (CS) zur Lösung von Incidents und Erarbeitung von Prozessverbesserungen</li>
	<li style="list-style-position:inside">Einführung eines Field Service Management Tools sowie &nbsp;Integration von Field Service Management Prozessen via SAP CS</li>
	<li style="list-style-position:inside">Projektmethodiken und -module: ABAP, SAP CS Modul, S/4Hana Service, SAP FSM und ServiceMaxx</li>
</ul>

&nbsp;

&nbsp;

Rahmendaten:&nbsp;

Start: 01.03.2023, spät 20.03.2023

Dauer: bis 31.12.2023

Auslastung: Durchschnittlich 5-10 Projekttage pro Monat 

Einsatzort: 95% remote
</div>

SAP Customer Services Expert

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">Experte Bioanalytik (M/W/D)
&nbsp;
Aufgaben:
<ul><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Selbstständige Planung und Durchführung von bioanalytischen Methoden, u.a., aber nicht ausschließlich, im Rahmen der LC-MS/MS-Methodiken zur (semi-)quantitativen Bestimmung der Konzentration von Proteinen und kleinen Molekülen aus Zellversuchen</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Präklinische und klinische Studien mittels LC-MS/MS Geräten</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Planung, Durchführung und Dokumentation der Probenvorbereitung an automatisierten Systemen</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Planung und Dokumentation der Experimente im LIMS, sowie in einem elektronischen Notebook gemäß den Grundsätzen der Guten Wissenschaftlichen Laborpraxis</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Zusammentragen der Ergebnisse sowie Auswertung und Interpretation der entsprechenden Daten u.a. mittels LIMS oder Excel</li></ul>
&nbsp;
Qualifikation:​​​​​​​
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Kenntnisse LC-MS/MS&nbsp;und&nbsp;UPLC-MS/MS</li><li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Erfahrung mit LIMS Systemen und Excel</li><li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Profunde Erfahrung im pharmazeutischen Umfeld</li></ul>
&nbsp;
Rahmendaten:&nbsp;
Start: ab sofort&nbsp;
Dauer: 11 Monate
Auslastung: 4-5 Tage die Woche&nbsp;
Einsatzort: Rheinland-Pfalz&nbsp;
&nbsp;
&nbsp;
&nbsp;
&nbsp;</div>

Experte Bioanalytik

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Regulatory Affairs Manager REACH (M/W/D) 
 
Aufgaben:

<ul>
	<li style="margin-left:8px;list-style-position:inside">Erstellung und Betreuung von REACH-Registrierungen</li>
	<li style="margin-left:8px;list-style-position:inside">Unterstützung von weiteren europäischen Standorten bei Registrierungsaktivitäten</li>
	<li style="margin-left:8px;list-style-position:inside">Kommunikation mit zuständigen Behörden</li>
	<li style="margin-left:8px;list-style-position:inside">Beratung über chemikalienrechtliche Entwicklungen</li>
</ul>

<div> 
Qualifikation:

<ul>
	<li style="margin-left:8px;list-style-position:inside">Erfahrung im Bereich Regulatory Affairs / Registrierungen für chemische Produkte/Stoffe</li>
	<li style="margin-left:8px;list-style-position:inside">Erfahrung im chemikalienrechtlichen Bereich (REACH)</li>
	<li style="margin-left:8px;list-style-position:inside">Profunde Kenntnisse in IUCLID</li>
	<li style="margin-left:8px;list-style-position:inside">Must-Have: Deutsch und Englisch fließend</li>
	<li style="margin-left:8px;list-style-position:inside">Hands-On Arbeitsweise</li>
</ul>
</div>

 
Rahmendaten: 
Start: Mitte Februar, spätestens Mitte März 23 
Dauer: 6 Monate 
Auslastung: 3-5 Tage 
Einsatzort: Vor Ort + Remote
</div>

Regulatory Affairs Manager REACH

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Galenik-Berater (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Beratung im Bereich Business Development</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Erstellen von Entwicklungsplänen, Forschungsberichte,&nbsp;Reportings</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Beratung in der Formulierungsherstellung</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Monitoring von Projekten</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">SOP-Management</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Studium im Bereich Pharmazie, Biotechnologie oder vergleichbare Disziplin</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Kenntnisse In den Bereichen GMP, ICH, CTD</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Fließend Deutsch und Englisch in Wort und Schrift</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Kenntnisse mit den gängigen Technologien zur Herstellung von Solida, Semisolida und flüssigen Arzneimitteln</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Nice-to-have: Erfahrung im Bereich 2D+3D-Druck&nbsp;</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: asap

Dauer: 3 Monate

Auslastung: 3-5 Tage die Woche

Einsatzort: Onsite (Großraum München) + Remote

&nbsp;

&nbsp;</div>

Galenik-Berater

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Veeva PromoMats Process Expert (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Consulting with the approval system of the promotional material in Veeva Vault</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Advising within change management, End-User request management and User access request in the day to day business operations&nbsp;</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Acting as a business SME of Vault PromoMats as well as an interface with the IT-departement</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Writing and designing of operational SOPs and dashboards</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Bachelor's degree in a scientific/engineering discipline</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Extensive Veeva Vault PromoMats platform experience (plus: Business administrator certification)</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">In-depth understanding of Veeva Vault System requirements and specifications</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Global Commercial background and profound IT understanding</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Must-have: Business fluent in English</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: asap

Duration: 6 months

Capacity: 25-40 hours per week

Location: remote with&nbsp;occasional trips&nbsp;

&nbsp;
</div>

Veeva PromoMats Process Expert

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">IT License Management Expert (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="list-style-position:inside">Screening and reduction of the backlog of software orders</li>
	<li style="list-style-position:inside">Preparation of Purchase Order Requisition for management approval</li>
	<li style="list-style-position:inside">Harmonization of the data stock in the Software Asset Management System</li>
	<li style="list-style-position:inside">Clarification of the possibilities of automation for license assignment processes</li>
	<li style="list-style-position:inside">Coordination and documentation of IT license management (Maintenance of license inventories)</li>
</ul>

&nbsp;&nbsp;

Requirements:&nbsp;

Start: 13.02.2023, latest 01.03.2023

Duration: until 30.10.2023

Capacity: 4 hours per day, 5 days a week

Location: 100% remote

&nbsp;</div>

IT License Management Expert

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Baustellenleiter/Construction Manager TGA (M/W/D)
&nbsp;
Aufgaben:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="box-sizing: border-box;">Schwerpunkt ist die Steuerung, Bauüberwachung und Koordination im Rahmen eines Neubauprojektes auf Bauherrenseite (LPH8); teilweise auch Bauen im Bestand</li><li style="box-sizing: border-box;">Erste/r Ansprechpartner/in auf der Baustelle für TGA-Themen und Schnittstelle zwischen Nutzer, externen Firmen, Generalplaner ggf. Generalunternehmer</li><li style="box-sizing: border-box;">Eigenständige Organisation und Durchführung von Begehungen, Abnahmen, Bau- und Planungsbesprechungen</li><li style="box-sizing: border-box;">Selbständige Planung, Steuerung und Überwachung von Terminen sowie die Zuarbeit zu Kosten- und Nachtragsmanagement</li><li style="box-sizing: border-box;">Eigenständige projektbezogene Qualitätskontrolle und -sicherung sowie Kontrolle und Freigabe von Aufmaßen in Abstimmung mit dem Kunden</li><li style="box-sizing: border-box;">Sicherstellung der Einhaltung der Baustellenordnung in Absprache mit dem SiGeKo und Übernahme der Baustellenkorrespondenz (z.B. bei Bedenkenanzeigen)</li></ul>
&nbsp;
Qualifikation:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="box-sizing: border-box;">Meister in einem technischen Beruf bzw. ein abgeschlossenes technisches Studium oder eine vergleichbare Qualifikation im&nbsp;TGA&nbsp;oder Anlagenbau</li><li style="box-sizing: border-box;">Ausgeprägte Kenntnisse auf dem Gebiet der Technischen Gebäudeausrüstung (HLKS)</li><li style="box-sizing: border-box;">Langjährige Projekterfahrung in der Abwicklung von komplexen Bauprojekten, bevorzugt in der Pharma-, Medizintechnik- oder Lebensmittelindustrie</li><li style="box-sizing: border-box;">Umfassendes Know-how in der Überwachung von Baustellen gemäß LPh 8</li><li style="box-sizing: border-box;">GMP-Kenntnisse sind wünschenswert</li><li style="box-sizing: border-box;">Sehr gute Deutschkenntnisse in Wort und Schrift</li></ul>
&nbsp;
Rahmendaten:&nbsp;
Start: 27.02.2023, spät. 13.03.2023
Dauer: 12 Monate
Auslastung: 5 Tage die Woche
Einsatzort: Pfaffenhofen</div>

Baustellenleiter/Construction Manager TGA

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">Senior Pharmaceutical Engineer (M/F/D)
&nbsp;
Tasks:
<ul><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Management of engineering equipment projects (GMP and non-GMP) </li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Ownership on continuous improvement in pharmaceutical production including troubleshooting, optimization and of equipment and processes</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Support / take over all kinds of additional technical tasks within the Campus Engineering department</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Close interaction with other department and leadership board </li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Provide consultancy to the local engineering teams at the manufacturing sites</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Strategical support in optimizing tech transfer projects and global engineering standards</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">LEAN Management </li></ul>
&nbsp;
Qualification:
&nbsp;
<ul style="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: 0cm;">Degree in pharmaceutical engineering or similar </li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Track Record in pharmaceutical engineering, ideally in manufacturing environment</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Knowledge of TPM, WCM environment, LEAN and SIX SIGMA and GMP</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Project management in pharmaceutical projects</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Fluency in business German and English, other languages are beneficial</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Nice to have: experience in digital transformation</li></ul>
&nbsp;
Requirements:&nbsp;
Start: asap
Duration: 6 months
Capacity: 4-5 days per week
Location: onsite &amp; remote
&nbsp;</div>

Senior Pharmaceutical Engineer

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Scientific Expert&nbsp;(M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="box-sizing: border-box;">Review scientific slide decks, corporate communications, PR and marketing materials, and other relevant documents for scientific accuracy.</li>
	<li style="box-sizing: border-box;">Review includes evaluating if reference used is appropriate and the material text is accurately describing the message of the original material. Review also includes evaluating if appropriate scientific language is used in the content and if product label is correctly referenced in the material and if material is deviating from the company product label it should be either clearly indicated in disclaimer or remover in the case of commercial material. Also materials going to public distribution for nonprescribers, nonpromotional and nonbranding approach should be used.</li>
	<li style="box-sizing: border-box;">When appropriate, reviewer can also point out inconsistencies in content compared to earlier materials in terms of wording used or references used.</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="box-sizing: border-box;">MSc or similar decree in life sciences, PhD or MD training would be necessary</li>
	<li style="box-sizing: border-box;">Project experience in reviewing and understating scientific material</li>
	<li style="box-sizing: border-box;">Experience with Veeva Promomats review system would be beneficial, but not mandatory</li>
	<li style="box-sizing: border-box;">English spoken and written necessary</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: 01.02.2023

Duration: 31.07.2023

Capacity: 2 days per week, remote

&nbsp;

&nbsp;</div>

Scientific Expert

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Projektmanager Entwicklung (M/W/D)

<div>&nbsp;</div>

<div>Aufgaben:</div>

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Optimierung von Projektmanagementtools</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Risikomanagements, inkl. Identifikation, Bewertung und Reduzierung von Risiken</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Erstellung von Projektplänen und -kalkulationen</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Controlling, Dokumentation und Änderungsmanagement</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">teilweise mehrere kleinere Projekte gleichzeitig koordinieren</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Schnittstellenmanagment mit Fertigung, Konstruktion und Entwicklung&nbsp;</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Reporting an Stakeholder</li>
</ul>

<div>&nbsp;&nbsp;&nbsp;</div>

<div>Qualifikation:</div>

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">profunde Kenntnisse im Projektmanagement des B2B-Bereichs, idealerweise im regulierten Umfeld oder des Sondermaschinenbaus</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Deutsch und Englisch fließend</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">gute Kenntnisse in MS Office</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">agile Hands-On Mentalität und Kommunikationsstärke</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Nice-to-have: Studium im Bereich Engineering</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Nice-to-have: Erfahrung mit der Entwicklung von Geräten der optischen Messtechnik</li>
</ul>

<div>&nbsp;</div>

<div>Rahmendaten:&nbsp;</div>

<div>Start: asap</div>

<div>Dauer: 6 Monate</div>

<div>Auslastung: 4-5 Tage die Woche</div>

<div>Einsatzort: Großraum Hamburg und remote</div>

<div>&nbsp;

&nbsp;

&nbsp;&nbsp;

&nbsp;
</div></div>

Projektmanager Entwicklung

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Project Engineer (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Projekt für Investitions-, Erweiterungs-, Sanierungs-, Umbau- und Instandhaltungsvorhaben</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Erstellung von Leistungsbeschreibungen sowie Bau- und Ausstattungsbeschreibungen</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Einschätzung der Einhaltung vertraglicher, technischer und rechtlicher Rahmenbedingungen sowie Arbeits- und Umweltschutzvorschriften</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Auswahl, Koordination und Betreuung sämtlicher externer Dienstleister im Verantwortungsbereich</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Erstellung von Bauanträgen ggf. unter Einbeziehung externer Ressourcen</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Organisation und Kontrolle der Bauaufsicht sowie Sicherstellung der Qualitätsanforderungen auf der Baustelle (vom Verbau bis zum Innenausbau)</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Erstellen von Projekt- bzw. Baufortschrittsberichten sowie Erstellung von Kennzahlen zur Beurteilung des Projektverlaufs</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Compliance-Überwachung der technischen, vertraglichen und rechtlichen Rahmenbedingungen sowie Gesundheits-, Sicherheits- und Umweltvorgaben</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Auswahl, Koordination und Überwachung von externen Unternehmen im Verantwortungsbereich</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">5 Jahre erfolgreiche Berufspraxis im Bereich des Baus von komplexen Gebäuden sowie in der Leitung von Projekten&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Sicherer Gebrauch von Methoden des Projektmanagements und deren Kontrollinstrumente</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Sicherer Gebrauch von üblichen Regularien, wie HOAI oder VOB</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">MS Office applications, MS Project, Primavera or similar as well as CAD/CAE</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: asap

Dauer: 12 Monate

Auslastung: 5 Tage die Woche

Einsatzort: onsite (Hessen) &amp; remote

&nbsp;

&nbsp;

&nbsp;

&nbsp;
</div>

Project Engineer

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Data Scientist - Machine Learning PIE (M/F/D)

&nbsp;&nbsp;

Tasks:

<div style="font-family:&quot;Open Sans&quot;,sans-serif; font-size:16px; line-height:normal; margin-bottom:0cm; margin-left:0cm; margin-right:0cm; margin-top:0cm">The goal is to extend and unify two versions of PIE into one consolidated data science product. The extensions are focused on two areas: scaling the two versions and implementing analyses for a new indication.</div>

<div style="font-family:&quot;Open Sans&quot;,sans-serif; font-size:16px; line-height:normal; margin-bottom:0cm; margin-left:0cm; margin-right:0cm; margin-top:0cm">&nbsp;The tasks include, among others:</div>

<ul>
	<li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 16px; line-height: normal; margin: 0cm;">Consult on tech stack decision and scale the current locally developed product to AWS</li>
	<li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 16px; line-height: normal; margin: 0cm;">Compare, optimize, and test existing Python code</li>
	<li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 16px; line-height: normal; margin: 0cm;">Unify existing code of two repositories to one with indication-specific modules</li>
	<li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 16px; line-height: normal; margin: 0cm;">Scale PIE to a new indication</li>
</ul>

&nbsp;&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">The freelancer should have multiple years of experience of professional code development in python and practical experience with the cloud service AWS</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Additionally,&nbsp;&nbsp;knowledge of unit testing and tools to work collaboratively on data science projects are mandatory</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">In particular, the &nbsp;candidate should be familiar with text processing, scaling existing prototypes and professionalize &amp; optimize existing code</li>
</ul>

<div>&nbsp;&nbsp;</div>

Requirements:&nbsp;&nbsp;&nbsp;&nbsp;

Start: 01.03.2023

Duration: 9&nbsp;months

Capacity: 5 days per week&nbsp;(20-50% onsite)&nbsp;&nbsp;

Location: Munich, Germany &amp; remote

&nbsp;</div>

Data Scientist - Machine Learning PIE

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Cyber Security Solution Architect (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Realization of Cyber Security Architecture reviews</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Analysing of security controls in the context of ISO27001</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Cyber Security Architecture certification such as SABSA</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">2-3 years experience as a Cyber Security Solution Architect</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Understanding of complex system architecture in on-perm or cloud context</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Know-how in: Threat Modelling, Business Impact Analysis, Business Context Analysis</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Must-have: Business fluent in English</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: asap

Duration: 6 months

Capacity: 4-5 days per week

Location: remote

&nbsp;
</div>

Cyber Security Architect

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Qualified Person (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; 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">Bearbeitung von Chargenfreigaben von ESO Produkten <span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#333333; 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:start; 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">(External Supplier Operations):&nbsp;<span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; 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">Fertigwaren, Halbfertigwaren und Bulk</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; 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">Produktunterlagen werden chargenweise übergeben (Print/elektronisch) zur unabhängigen, eigenständigen Überprüfung und Bewertung zur Freigabeentscheidung.</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; 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">Verwendungsentscheid / Rückgabe</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; 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">Die Statusänderung der Chargen wird im System (SAP) umgesetzt und auf den Unterlagen (Print/elektronisch) dokumentiert. Rückgabe der Unterlagen (Print/elektronisch) nach Umsetzung des Freigabeentscheids mit Freigabevermerk. Falls keine Freigabe erfolgen kann, Rückgabe der Unterlagen (Print/elektronisch) mit Vermerk zum Ergebnis der Chargenüberprüfung, des getroffenen Verwendungsentscheids und Kommunikation zum Ergebnis der Chargenbewertung sowie Handlungsempfehlung an den SPOC / Single Point of Contact (elektronisch)</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; 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">Verantwortlich für die eigenverantwortliche, eigenständige, GMP konforme und termingerechte Bearbeitung der Chargenbewertungen und Chargenfreigaben in Übereinstimmung mit allen allgemeinen gesetzlichen Vorgaben sowie Novartis-internen SOPs (Standard Operating Procedure) und Qualitätsstandards</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; color:#000000; 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:start; 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">Sachkundige Person/Qualified Person gem. AMG §15&nbsp;und Anerkennung als Sachkundige Person durch die örtliche Behörde.</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; color:#000000; 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:start; 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">Erfahrung im Bereich&nbsp;<span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; 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">ESO Produkten (Fertigwaren, Halbfertigwaren und Bulk), idealerweise:&nbsp;Tabletten, Filmtabletten und Kapseln zur oralen Einnahme, vorallem&nbsp; hochwirksame Arzneimittel zur Krebstherapie.&nbsp;</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; color:#000000; 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:start; 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">Tiefgehende GMP Kenntnisse</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; color:#000000; 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:start; 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">Must have: Fließend Deutsch &amp; Englisch</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: asap

Dauer: bis 30.06.2023

Auslastung: 2-3 Tage die Woche

Einsatzort: Barleben, Sachsen-Anhalt
</div>

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div>Einer unserer Pharma-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
 
Clinical Research Associate&nbsp;(M/F/D) 
 
Aufgaben:
<ul>
	<li style="list-style-position:inside">Klinisches Monitoring bei aktuellen Studien (Phase 2-3)</li>
	<li style="list-style-position:inside">Studien Vorbereitung / Study Start up </li>
	<li style="list-style-position:inside">Qualification &amp; Initiation Visits</li>
	<li style="list-style-position:inside">Einreichungsprozesse (Vorbereitung Ethikeinreichungen)</li>
	<li style="list-style-position:inside">Betreuung der Studien</li>
	<li style="list-style-position:inside">Erstellung von Studiendokumenten</li>
</ul>
 
Qualifikation:

<ul>
	<li style="list-style-position:inside">Erfolgreich abgeschlossenes Naturwissenschaftliches Studium</li>
	<li style="list-style-position:inside">Mehrjährige CRA Erfahrung </li>
	<li style="list-style-position:inside">Erfahrung mit Risk- based Monitoring (RBM)</li>
	<li style="list-style-position:inside">Erfahrung im Bereich Vakzine / Kardiologie / Onkologie&nbsp;</li>
	<li style="list-style-position:inside">Hands-on Mentalität, Lösungsorientiert</li>
	<li style="list-style-position:inside">Reisebereitschaft DE</li>
	<li style="list-style-position:inside">Verhandlungssicher in Deutsch &amp; Englisch</li>
</ul>
 
Rahmendaten: 

<ul>
	<li style="list-style-position:inside">Start: ab sofort &nbsp;</li>
	<li style="list-style-position:inside">Dauer: 12 Monate plus</li>
	<li style="list-style-position: inside;">Auslastung: 20-25 Stunden pro Woche remote </li>
</ul>
</div>
</div>

<div data-wrapper="true" style="font-family:Arial; font-size:10pt">
QA Expert (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="list-style-position:inside">Approval of&nbsp; APIs&nbsp;</li>
	<li style="list-style-position:inside">Creation, processing and approval of: Deviations, Complaints, Change requests manufacturing process and technology -and Process validations&nbsp;</li>
	<li style="list-style-position:inside">Approval of stability plans and assessment of stability deviations</li>
	<li style="list-style-position:inside">Execution of self-inspections</li>
	<li style="list-style-position:inside">Creation and harmonization of SOPs, including process flows according to GMP</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="list-style-position:inside">Systems: SAP, TrackWise</li>
	<li style="list-style-position:inside">Deep knowledge within GMP&nbsp;</li>
	<li style="list-style-position:inside">Business English &amp; German</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: 03.04.2023

Duration: until 29.09.2023

Capacity: 5 days per week

Location: remote

&nbsp;&nbsp;
</div>

QA Expert

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Project Engineer Process Equipment (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Develop Design in alignment with global and local in collaboration with project team members, EPCM company and local Engineering</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Support EPCM company for bid packages and participate of vendors selection to guarantee design and project requirements </li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Follow-up equipment construction and participate to FAT execution</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Secures optimal flow of technical information with project teams and local Engineering as well as any other relevant stakeholders.&nbsp; Promotes &amp; ensures global standard adherence and that necessary deviations are highlighted, discussed, well justified and documented</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Support CQV team to develop qualifications strategy and CQV documents. Be part of the CQV execution to identify corrective actions and close punch list according to initial design requirements </li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Support project control team for schedule and cost control</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Ensuring compliance with all pertinent safety policies, rules and regulations</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Bachelors or master’s degree in engineering or long time and in-depth project technical management or operational experience in international environments</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">5+ years experience in project engineering, project management and/or operations for chemical, biochemical, pharmaceutical industries, facility layout and optimization or equivalent</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Experience in the field of process equipment, Utilities and clean rooms design, layout and construction</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Excellent knowledge of current and proposed future technology in the field of process, associated automation, CQV, operation and maintenance</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Experience with cGMP regulatory requirements&nbsp;</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Knowledge of digital platform like Kneat, unifier, Trackwise </li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Language skills:&nbsp;English fluent / German advantageous </li>
</ul>

<div style="font-family:&quot;Open Sans&quot;,sans-serif; font-size:16px; line-height:normal; margin-bottom:0cm; margin-left:0cm; margin-right:0cm; margin-top:0cm">&nbsp;</div>

<div>Requirements:&nbsp;</div>

Start: 01.02.2023

Duration: 12 months

Capacity: 5 days per week

Location: Switzerland&nbsp;

&nbsp;</div>

Project Engineer Process Equipment

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Automation Engineer&nbsp;(M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Erstellung &amp; Review von Lastenheften</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Überprüfung von Detaildesign und technischen Dokumenten</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Überprüfung von FAT-Plänen</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Abschluss von FAT-Aktivitäten</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Vorbereitung der FAT-Dokumentation&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Überprüfung der SAT-Pläne</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Überwachung der Implementierung der Ausrüstung</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Beratungstätigkeiten hinsichtlich bei der Inbetriebnahme</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Begleitete Durchführung FAT/SAT</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Überwachung von relevanten Korrekturmaßnahmen</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Überprüfung der Abschlussdokumentation</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Validierungstätigkeiten (Funktionstests,…)</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Koordinationstätigkeiten mit Lieferanten &amp; internen Abteilungen (IT, Produktion, Electrical Engineering)</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Dokumentationstätigkeiten&nbsp;</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Profunde Erfahrung im Bereich Automation Engineering</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Must have:&nbsp;PCS7 Erfahrung</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Sprachkenntnisse: Deutsch &amp; Englisch&nbsp;</li>
</ul>

<div style="font-family:&quot;Open Sans&quot;,sans-serif; font-size:16px; line-height:normal; margin-bottom:0cm; margin-left:0cm; margin-right:0cm; margin-top:0cm">&nbsp;</div>

Rahmendaten:&nbsp;

Start: 01.02.2023

Dauer: 12 Monate

Auslastung: 5 Tage die Woche

Einsatzort: Österreich &amp; remote

&nbsp;</div>

Automation Engineer

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Migration of MS Project Server Expert (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="list-style-position:inside">Teilarbeitspaket im Rahmen eines M&amp;A Integrationsprojekts</li>
	<li style="list-style-position:inside">Durchführung einer Migration von MS Project Servern aus einer externen Domain in die Sartorius Domain</li>
	<li style="list-style-position:inside">Integration von 42 Nutzern von MS Project Servern </li>
</ul>

&nbsp;

&nbsp;

Rahmendaten:&nbsp;

Start: asap, spät. 02.01.2023

Dauer: bis 06.02.2023

Auslastung: 5 Tage die Woche

Einsatzort: remote</div>

Migration of MS Project Server Expert

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Marketing Quality Manager (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Advising the Global Marketing Team in the field of quality management</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Providing processes and tools for quality document and record management, trainings and CAPA management</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Performing of quality planning and quality reviews</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Consulting on process analysis, process design and quality improvement</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Cross-functional working to drive Marketing quality initiatives forward and to resolute quality issues</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Advising in how to improve and standardize processes in the Global Marketing Team&nbsp;&nbsp;</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Several years of experience in marketing at a pharmaceutical company</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Broad experience in setting up quality processes in marketing in a global company</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Business fluency in English</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Experience working ex-Europe is a plus</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: asap

Duration: 6 months

Capacity: 4-5 days per week

Location: remote

&nbsp;
</div>

Marketing Quality Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Interim Head Quality (M/W/D) 
 
Aufgaben:

<ul>
	<li style="margin-left:8px;list-style-position:inside">Beratende Unterstützung als QP nach AMG und zu allgemeinen Themen rund um das Betäubungsmittelgesetz </li>
	<li style="margin-left:8px;list-style-position:inside">Capa- , Abweichung- und Reklamations- Management</li>
	<li style="margin-left:8px;list-style-position:inside">Qualitative Überprüfung der Dokumentation in Verpackung sowie in der Fertigung </li>
	<li style="margin-left:8px;list-style-position:inside">Einführung und Pflege einer effizienten Aufbau- und Ablauforganisation im Verantwortungsbereich, Zusammenarbeit mit anderen Funktionen zur Optimierung der Schnittstellen</li>
	<li style="margin-left:8px;list-style-position:inside">Beratung und fachliche Anweisung der Mitarbeiter in der Produktion </li>
	<li style="margin-left:8px;list-style-position:inside">Nachhaltige Entwicklung und Optimierung der Prozesse und Beseitigung von Prozessoptimierungen oder Produktverlagerungen</li>
	<li style="margin-left:8px;list-style-position:inside">Zusammenarbeit mit anderen Abteilungen und Stakeholdern zur Beschaffung von Informationen, und zur Erfüllung von gesetzlichen Anforderungen, Stand der Technik und Sicherheitstechnik sowie Verfahrensentwicklung</li>
</ul>

<div> 
 
Qualifikation:

<ul>
	<li style="margin-left:8px;list-style-position:inside">Qualified Person nach §15 AMG</li>
	<li style="margin-left:8px;list-style-position:inside">Langjährige Führungserfahrung im GMP-Umfeld, idealerweise in der Quality oder Production-Umfeld </li>
	<li style="margin-left:8px;list-style-position:inside">Erfahren in der Umsetzung von Projekten </li>
	<li style="margin-left:8px;list-style-position:inside">Idealerweise Btm-Verantwortlicher nach § BtMG 3</li>
	<li style="margin-left:8px;list-style-position:inside">Fließende Deutsch und Englisch-Kenntnisse</li>
</ul>
</div>

 
Rahmendaten: 
Start: Ab sofort, spätestens Anfang Februar 
Dauer: 6 Monate 
Auslastung: mind. 4 Tage / Woche 
Einsatzort: NRW &amp; remote
</div>

Interim Head Quality (M/W/D)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Interim Head of Quality (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Interimistische Leitung Quality </li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Interimistische Funktion als fachlicher Ansprechpartner für die Abteilung QA/QC</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Ausbau des standortübergreifenden QM-System</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">CAPA- und Abweichungsmanagement</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Durchführung von PQRs&nbsp;</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Change Control&nbsp;</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Review von SOPs</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Vorbereitung und Begleitung von Audits und Inspektionen</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Naturwissenschaftliches Studium oder vergleichbare Qualifikation</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Langjährige Erfahrung im pharmazeutisch-regulierten Umfeld</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Profunde Kenntnisse gängiger Regularien (GMP)&nbsp;</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Erfahrung als Leitung Quality</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Sprachkenntnisse: Deutsch &amp; Englisch&nbsp;</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: 01.02 spätestens 01.04

Dauer: 3 - 6 Monate

Auslastung: 3 - 4 Tage die Woche

Einsatzort: Nordrhein-Westfalen&nbsp;
</div>

Interim Head of Quality

<div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Junior Project Manager (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Plan and schedule project timelines and milestones</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Develop, maintain and effectively execute project plans throughout the project life. Ensure timely revision of project plan to meet changing needs and requirements</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Define, communicate, implement and monitor quality standards on all project deliverables</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Manage day-to-day operational aspects of the project</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Plan and manage internal and external project communications, ensuring effective exchange of project information and deliverables</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Assists in the ongoing development of the Project Management Office. Recommend improvements to project management policies/procedures where needed</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Identify, analyze, prioritize, mitigate and communicate project risks</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Serve as liaison between company and client for the overall project and support activities.</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">3+years of Project Management Experience</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Business fluent in English<span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Proficient understanding of MS Office</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Project Management Professional Certification</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Experience with specific project management methodologies such as Scrum and Agile</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Broad understanding of typical enterprise applications, IT infrastructures, public and on-premises cloud, including but not limited to CRM technologies</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: 23.01.23, latest 06.02.23

Duration: until 22.07.23

Capacity: 5 days per week

Location: Zug, Switzerland

&nbsp;
</div>

Junior Project Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
One of our Medical Device Clients in Germany is currently seeking a:&nbsp;

&nbsp;

Medical Consultant Urology (M/W/D) 
&nbsp;

Tasks:

<ul>
	<li style="list-style-position:inside">Preparation of medical documents</li>
	<li style="list-style-position:inside">Documentation of Risk Management Plans</li>
	<li style="list-style-position:inside">Medical evaluation and assessments</li>
	<li style="list-style-position:inside">Support in post-market surveillance (PMS)</li>
	<li style="list-style-position:inside">Contact person for medical questions</li>
	<li style="list-style-position:inside">Crossfunctional cooperation with various departments (Development / Regulatory / Quality)</li>
</ul>

<div>&nbsp; 
Qualifications:

<ul>
	<li style="list-style-position:inside">Medical degree in urology&nbsp;(min. 5 years of experience)</li>
	<li style="list-style-position:inside">Experience in Medical Device Regulation (MDR)</li>
	<li style="list-style-position:inside">Familiar with Extracorporeal shockwave therapy (ESWT) and Extracorporeal shockwave lithotripsy (ESWL)</li>
	<li style="list-style-position:inside">Experienced in Medical Writing</li>
	<li style="list-style-position:inside">Fluent in English</li>
</ul>
</div>

&nbsp; 
Requirements: 
Start: January 2023 
Duration: 18 months++ 
Capacity: tbd 
Location: remote
</div>

Medical Consultant Urology (M/W/D)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Digital Marketing Manager&nbsp;(M/F/D)

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Responsible&nbsp;for planning, monitoring and controlling of campaigns based on KPIs, benchmarks and insights</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Responsibile&nbsp;for the implementation of CANVAS and agency onboarding</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Advising the brand teams with regard to channels and platforms that are available and can be used nationwide Product brand-specific cross-media national and international campaigns</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Broad experience in the application of cross-media communication tools (with a focus on digital media)&nbsp;&nbsp;</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Exprience in the pharmaceutical industy with prescription products, ideally in the area of rare diseases</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Fluent German and very good English skills</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: 01.01.2023

Duration: 6-12 months

Capacity: 5 days per week

Location: Remote
</div>

Digital Marketing Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Medizintechnik-Kunden in NRW&nbsp;sucht aktuell freiberufliche Unterstützung als:

&nbsp;

Senior Manager RA/QA (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Regulatory Affairs

	<ul>
		<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Durchführung von Produktregistrierungen&nbsp;</li>
		<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Kommunikation mit zuständigen Behörden und Zertifizierungsstellen&nbsp;</li>
		<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Durchsetzung der Einhaltung notwendiger Vorschriften (IVDR)</li>
		<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Beratungstätigkeiten zur Erlangung und Aufrechterhaltung des Marktzugangs für alle Produkte&nbsp;</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Koordinierung und Durchführung der Post Market Surveillance</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Beratungstätigkeiten zur Vorbereitung auf die Einhaltung der neuen IVDR</li>
	</ul>
	</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Quality&nbsp;
	<ul>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Weiterentwicklung des Qualitätsmanagementsystems sowie der Qualitätsziele</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Durchführung des Management-Review-Prozesses</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Tätigkeiten im Rahmen der Qualitätsaufsicht des Produktionsbereiches</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Vorbereitung und Koordination von internen und externen Audits</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Lieferkettenmanagement </li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Management von Qualitätssicherungsvereinbarungen</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Dokumentation des Änderungsprozesses im Rahmen der Qualitätsmanagementprozesse</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">CAPA-Management</li>
	</ul>
	</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">R&amp;D&nbsp;
	<ul>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Koordinierung von Produktentwicklungsprojekten, Designänderungen und Änderungsaufträgen</li>
	</ul>
	</li>
</ul>

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Technisches Studium oder vergleichbare Qualifikation</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Min. 5 Jahre Erfahrung im RA/QA Bereich in einem IVD-, Medizinprodukte- oder Pharmaunternehmen</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Erfahrung in Funktionen als QMR und/oder Sicherheitsbeauftragter</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Erfahrung in der In-vitro-Diagnostik &amp; IVRD&nbsp;sowie&nbsp;Bereich der IVD- oder Assay-Entwicklung</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Kenntnisse molekularbiologischer Methoden&nbsp;</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Management-Fähigkeiten: Wünschenswert</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Erfahrung in RT-PC</li>
</ul>

Rahmendaten:&nbsp;

Start: 16.01.23 spät. 01.03.23

Dauer: 16 Monate

Auslastung: 3 - 5 Tage die Woche

Einsatzort: NRW &amp; remote&nbsp;

&nbsp;
</div>

Senior Manager RA/QA (M/W/D)

<div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Senior CRA (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Manage clinical study - Phase 1</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Monitoring activities, such as review of study protocols</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Clinical Project Management</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Manage Central Labs&nbsp;</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Profound experience as Senior CRA, Clinical Project Manager, Clinical Monitoring</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Experience with Phase 1 Studies</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Keen in writing and reviewing clinical protocols</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Nice to have: Experience within Oncology</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Detail-oriented, precise, high-quality standards</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: asap, latest beginning of 2023

Duration: 12-18 months

Capacity: 3-4 days per week

Location: California, but 100% Remote

&nbsp;
</div>

Senior CRA

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Beratungsleistung im Bereich Accounting (M/W/D)

&nbsp;

Aufgaben:

<ul style="unicode-bidi:embed" type="disc">
	<li style="vertical-align:middle">Eigenständige Durchführung von Projekten zur Optimierung der Accounting-Prozesse sowie zur Transformation der EU Finance Shared Services, insbesondere im Hinblick auf Leistungsportfolio, Aufbauorganisation, Prozesse und Systeme. Folgende Projektinhalte sind hierbei relevant:</li>
	<li style="vertical-align:middle">Beratungsleistung bei der qualitäts- und zeitgerechten Erstellung der Monats-, Quartals- und Jahresabschlüsse für ausgewählte Tochtergesellschaften nach IFRS, lokalem Handelsrecht und lokalem Steuerrecht durch das Shared Services Team</li>
	<li style="vertical-align:middle">Beratungsleistung hinsichtlich des Monitorings der SAP-Nebenbücher Bank-, Anlagen-, Debitoren- und Kreditorenbuchhaltung in SAP ECC, Intercompany-Buchungen und Kontenabstimmungen etc. gemäß IFRS, lokaler Rechnungslegung und Steuerrecht im Rahmen des o.g. Projektes</li>
	<li style="vertical-align:middle">Beratungsleistung bei der Sicherstellung der effizienten und zeitgerechten Bearbeitung von Lieferantenrechnungen über den elektronischen Rechnungsworkflow</li>
	<li style="vertical-align:middle">Beratung der EU Finance Shared Services sowie der internen Fachbereiche in der Europa-Zentrale und den lokalen Finance Teams in allen Accounting-bezogenen Fragen</li>
	<li style="vertical-align:middle">Fachlicher Ansprechpartner/-in für Betriebsprüfer, Steuerberater und Wirtschaftsprüfer</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="box-sizing: border-box;">Wirtschaftswissenschaftliches Studium und/oder vergleichbare kaufmännische Ausbildung</li>
	<li style="box-sizing: border-box;">Langjährige Projekterfahrung im&nbsp;Accounting/ Rechnungswesen eines mittelgroßen oder großen Unternehmens, idealerweise im Pharma-Umfeld und/oder in der Wirtschaftsprüfung</li>
	<li style="box-sizing: border-box;">Berufstitel als Wirtschaftsprüfer und/oder Bilanzbuchhalter/in international von Vorteil</li>
	<li style="box-sizing: border-box;">Langjährige und sehr fundierte Projekterfahrung in der Erstellung von Monats-, Quartals- und Jahresabschlüssen sowie in der Buchung von Intercompany-Geschäftsvorfällen, in der elektronischen Rechnungsverarbeitung und im Asset Accounting</li>
	<li style="box-sizing: border-box;">Langjährige und sehr fundierte Projekterfahrung als Interim Manager mit der Fähigkeit</li>
	<li style="box-sizing: border-box;">Umfangreiche Projekterfahrung in der Projektleitung im Finance-Bereich, idealerweise im Kontext von Transformationen oder der Planung und Implementierung von Shared-Service-Strukturen</li>
	<li style="box-sizing: border-box;">Sehr gute Kenntnisse nach&nbsp;IFRS, HGB und relevantem Steuerrecht erforderlich</li>
	<li style="box-sizing: border-box;">Sehr gute Kenntnisse in&nbsp;SAP R/3 bzw. SAP ERP (MM, FI), sehr gute MS-Office-Kenntnisse erforderlich</li>
	<li style="box-sizing: border-box;">Verhandlungssichere&nbsp;Deutsch- und Englischkenntnisse&nbsp;in Wort und Schrift erforderlich</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: 05.12.2022, spät. 12.12.2022

Dauer: 30.11.2023

Auslastung: 5 Tage die Woche, min. 2 Tage/Woche vor Ort

Einsatzort: München &amp; remote
</div>

Beratungsleistung im Bereich Accounting

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Interim Leiter der Fertigung Sondermaschinenbau (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Fachliche Führung von 100 Mitarbeitern</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Effektivitätssteigerung der aktuellen Fertigung im Bereich Sondermaschinenbau</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Begleitung der Einführung eines neuen ERP-Systems</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Erfahrung mit GMP-Regularien</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Must-have: Erfahrung im Bereich Kleinserienfertigung oder Sondermaschinenbau</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: ab sofort, spät. Februar 2023

Dauer: 18 Monate

Auslastung: Vollzeit, vor Ort

Einsatzort: Sachsen</div>

Interim Leiter der Fertigung

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
CAD-Konstrukteur (M/W/D)

 
Aufgaben:

<ul>
	<li style="margin-bottom:11px;list-style-position:inside">Annahme von Aufträgen für Sonderteilen, Klärung von Auftragsdetails mit Kunden und techn. Innendienst</li>
	<li style="margin-bottom:11px;list-style-position:inside">Erstellen von CAD-Zeichnungen (SolidWorks)</li>
	<li style="margin-bottom:11px;list-style-position:inside">Erteilen des Auftrages an unsere Lieferanten im In- und Ausland und der Dienstleister, Überwachung des Auftrages, Prüfen bei Fertigstellung</li>
	<li style="margin-bottom:11px;list-style-position:inside">Verwaltung von Teilen (Ein- und Ausbuchung der Teile im ERP)</li>
	<li style="margin-bottom:11px;list-style-position:inside">Koordination mit der Werkstatt sowie Machbarkeitsprüfung</li>
	<li style="margin-bottom:11px;list-style-position:inside">Sicherung und Einhaltung der Abbauprozesse und des QM</li>
	<li style="margin-bottom:11px;list-style-position:inside">Suche nach Ersatzlieferanten und Ersatzdienstleistern</li>
	<li style="margin-bottom:11px;list-style-position:inside">Vorschau und Lagerbestandssicherung von Teilen und Fertigprodukten</li>
	<li style="margin-bottom:11px;list-style-position:inside">Mitwirkung bei der Entwicklung neuer Produkte</li>
</ul>

<div>Qualifikation: 
&nbsp;
<ul>
	<li style="list-style-position:inside">Qualifikation als Konstrukteur / Techniker / Verfahrenstechniker</li>
	<li style="list-style-position:inside">Erfahrungen im Behälterbau / Anlagenbau / Rohrleitungsbau im Bereich Life Science (zwingend erforderlich)</li>
	<li style="list-style-position:inside">Fliessend Deutsch und Grundkenntnisse in Englisch</li>
</ul>
</div>

&nbsp; 
Rahmendaten:&nbsp; 
Start: ab sofort 
Dauer: 12 Monate (+Übernahme) 
Auslastung: 5 Tage die Woche vor Ort 
Einsatzort: nähe Zürich 
&nbsp; 
&nbsp;
</div>

CAD-Konstrukteur

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer&nbsp;Pharma-Kunden in Deutschland&nbsp;sucht aktuell freiberufliche Unterstützung als: 
 
Qualified Person (M/W/D) 
 
Aufgaben:

<ul>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Chargenfreigabe</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Auswertung der Chargenprotokolle</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Batch Records </li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">CAPA-Management</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Abteilungsübergreifende GMP-Beratung</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Risikobewertungen für alle Marktprodukte im Verantwortungsbereich</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Prozessoptimierung in der Produktion</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Troubleshouting</li>
</ul>

<div>Qualifikation:

<ul>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Sachkundige Personen gemäß § 15 AMG</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Solide Berufserfahrung im Produktionsumfeld</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Erfahrung im Bereich Orale Arzneimitteln (Brausetabletten, Suspension)</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Langjährige Erfahrung im Pharma Bereich</li>
</ul>
</div>

Must have: Deutsch, idealerweise auch gute Englischkenntnisse

&nbsp;

&nbsp;

<div style="list-style-position:inside; margin-bottom:11px; margin-left:16px">Rahmendaten: 
Start: asap, spätestens zum 01.01.2023 
Dauer: 6 Monate 
Auslastung1-2 FTE 
Einsatzort: Onsite</div>
</div>

Qualified Person (M/W/D)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Systemingenieur (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Realisierung und Justierung von optischen Aufbauten</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Messung elektrischer Signale mit Oszilloskop</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Verfassen und Review von komplexen Dokumentationen</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Lesen von Schaltplänen</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Aufnahme und Auswertung von Messdaten</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Verfassung und Prüfung von FMEAs, Unterstützung Risikomanagement</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Analyse und (Weiter-)Entwicklung der Systemarchitektur</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Planung und Durchführung von Verifikationstests- und Messungen</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Studium im Bereich Mechatronik, Engineering oder vergleichbar</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Profunde, praktische Erfahrung in der Spezifikation und Konzeptentwicklung komplexer Systeme (Hard- und Software)</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Erfahrung in der Entwicklung von Geräten in der Medizintechnik</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Deutsch und Englisch fließend</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Lösungsorientiert, holistischer Blick</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: ab sofort, spätestens 01.12.2022

Dauer: 6 Monate +

Auslastung: bestenfalls Vollzeit, mindestens 3 Tage / Woche

Einsatzort: Thüringen &amp; Remote&nbsp;
</div>

Systemingenieur

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Lifecycle Projektmanager / Change Manager (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li class="paragraph" style="list-style-position:inside;">Koordination, Überwachung und Umsetzung der Projekt- Ressourcen- und Maßnahmenplanung im Lifecycle-Management </li>
	<li class="paragraph" style="list-style-position:inside;">Pflege der Ticket-Übersicht (Abwicklung, Bündelung, Bewertung, Koordination)&nbsp; </li>
	<li class="paragraph" style="list-style-position:inside;">Interdisziplinäre Zusammenarbeit mit dem Lifecycle-Team, Moderation der Meetings </li>
	<li class="paragraph" style="list-style-position:inside;">Erstellung und Pflege der Dokumentationen im Änderungsmanagement</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li class="paragraph" style="list-style-position:inside">Studium im Bereich Ingenieurswissenschaft, Physik oder einer vergleichbar</li>
	<li class="paragraph" style="list-style-position:inside">Erfahrung in der Leitung von Entwicklungsprojekten&nbsp;</li>
	<li class="paragraph" style="list-style-position:inside">Erfahrung in der Entwicklung sicherheitskritischer medizintechnischer Systeme, idealerweise im Lifecycle-Management medizinischer Geräte&nbsp;</li>
	<li class="paragraph" style="list-style-position:inside">Kenntnisse ISO 13485, 60601</li>
	<li class="paragraph" style="list-style-position:inside">Deutsch fließend</li>
	<li class="paragraph" style="list-style-position:inside">Kommunikationsstärke, sehr gute Projektmanagementkenntnisse</li>
</ul>

Rahmendaten: 
Start: ab sofort, spätestens 01.12.22 
Dauer: 6 Monate + 
Auslastung: 4-5 Tage die Woche 
Einsatzort: Thüringen &amp; Remote (nach Einarbeitung flexibel)
</div>

Lifecycle Projektmanager / Change Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Pharma-Kunden in NRW&nbsp;sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Experte Category Management&nbsp;(M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Implementierung / Optimierung eines Category Managements</li>
	<li>Beratung hinsichtlich der Strategieentwicklung einzelner Warengruppen&nbsp;&nbsp;</li>
	<li>Purchase Order Management innerhalb verschiedener Warengruppen&nbsp;</li>
	<li>Optimierung von Einkaufsprozessen&nbsp;</li>
</ul>

Qualifikation:

<ul>
	<li lang="de" style="vertical-align: middle;">Weitreichende Expertise im Bereich Category Management&nbsp;</li>
	<li lang="de" style="vertical-align: middle;">Strategische Expertise sowie Kenntnisse im operativen Beschaffungsmanagement </li>
	<li lang="de" style="vertical-align: middle;">Erfahrung im Bereich des Konzerneinkaufs sowie ein hohes Gesamtprozessverständnis&nbsp;</li>
	<li>Erfahrung im SAP-ERP System</li>
	<li>Sehr gute Englischkenntnisse</li>
</ul>

Rahmendaten: 
Start: Ab sofort / Spätestens 01.01.23 
Dauer: 6 Monate 
Auslastung: 3-5 Tage die Woche 
Einsatzort: Vor Ort &amp; remote&nbsp;

&nbsp;

&nbsp;
</div>

Experte Category Management (m/w/d)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Experte Hardwareentwicklung (m/w/d) 
&nbsp; 
Aufgaben:

<ul>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie ent­wick­eln ana­lo­ge und di­gi­ta­le Schal­tun­gen</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie er­stel­len elek­tri­sche Schalt­plä­ne/Lay­outs für hoch­in­te­grier­te Sys­te­me</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie haben Er­fah­rung in der Elek­tro­nik HW-Ent­wick­lung in den Be­rei­chen Schal­tungs­ent­wurf, Si­mu­la­ti­on und Lei­ter­plat­ten­lay­out</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie steuern die Nach­hal­ti­ge Do­ku­men­ta­ti­on der Ent­wick­lungs­er­geb­nis­se</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie steuern die Durch­füh­rung und Be­glei­tung von Va­li­die­rungs- und Qua­li­fi­zie­rungs­prü­fun­gen (in­tern und ex­tern)</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie ver­fü­gen über ein mit gutem Er­folg ab­ge­schlos­se­nes (Fach-) Hoch­schul­stu­di­um im Be­reich Elek­tro­tech­nik, Nach­rich­ten­tech­nik (oder ver­gleich­ba­rer Stu­di­en­gang)</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie haben über 3 Jahre Er­fah­rung in der Ent­wick­lung von Mi­xed-Si­gnal-Elek­tro­nik­ge­rä­ten oder vergleichbares&nbsp;</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Er­fah­rung im Um­gang mit La­bor­ge­rä­ten und Mess­in­stru­men­ten</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Er­fah­rung im De­bug­ging von Lei­ter­plat­ten-Bau­grup­pen, ein­schlie­ß­lich Löten von SMD-Bau­tei­len</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Er­fah­rung in der Er­stel­lung von Lay­outs be­züg­lich High-Speed-In­ter­faces, Mi­kro­con­trol­ler und Pro­zes­so­ren</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie haben einen si­che­ren Um­gang mit min­des­tens einem E-CAD-Pro­gramm</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie ken­nen sich in ent­wick­lungs­be­glei­ten­den The­men­fel­dern wie EMV- und Um­welt­an­for­de­run­gen gut aus</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Gute Sprach­kennt­nis­se in Deutsch und wer­den vor­aus­ge­setzt sowie sehr gute Eng­lisch­kennt­nis­se in Wort und Schrift</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Team­fä­hig­keit, Um­set­zungs­stär­ke und Ziel­ori­en­tie­rung, ef­fi­zi­en­tes Selbst­ma­nage­ment und ein hohes Maß an Zu­ver­läs­sig­keit</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Nice to have: Er­fah­rung mit Ge­rä­ten der Leis­tungs­elek­tro­nik</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Nice to have: Er­fah­rung mit dem Pro­gramm Al­ti­um De­si­gner</li>
	<li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">&nbsp;</li>
</ul>

Rahmendaten: 
Start: sofort&nbsp; 
Dauer: 6 Monate 
Auslastung: 5 Tage die Woche vor Ort&nbsp; 
Einsatzort: Baden-Württemberg

&nbsp;

&nbsp;

&nbsp;

&nbsp;
</div>

Ingenieur in der Hardwareentwicklung (m/w/d)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div>Clinical Site Manager (M/F/*) 
&nbsp; 
Special emphasis lies on: 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience with study-start-up activities 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Patient Recruitment 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Site oversight and proactive/forward-looking issue management 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Capability to liaison with CRAs, KOLs, PIs (relationship management) 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Document &amp; track monitoring 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Support site audit preparations 
&nbsp; 
Qualifications&nbsp;: 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Extensive experience with site management &amp; oversight, monitoring processes 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Being able to act as trouble-shooter and create high-performance environment 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; History of ensuring GCP adherence and applying risk management 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience with highly complex studies 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 5+ years of PM and 3+ years of monitoring 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Very good communication &amp; organizational skills 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Business fluency in Turkish &amp; English 
&nbsp; 
Requirements: 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Start: asap, there is some flexibility 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; FTE: full-time would be ideal 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Duration: 6 – 12 months 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Location: remote + travel as far as possible within Turkey, most sites are in Istanbul 
&nbsp;</div>
</div>

Clinical Site Manager // Study Project Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Kunden aus dem Bereich Biotech/Medical Device in Deutschland sucht derzeit freiberufliche Unterstützung als:

2-3x Sales Agent Germany Surgery (D/M/W) 
Regionen: Bayern, Nord-Ost (vielleicht Baden-Württemberg)&nbsp; 
 
 
Aufgaben:

<ul>
	<li style="list-style-position: inside;">Aktive und enthusiastische Entwicklung des deutschen Marktes</li>
	<li style="list-style-position: inside;">Erreichen von Vertriebszielen</li>
	<li style="list-style-position: inside;">Betreuung aktiver und potenzieller Kunden auf produkt- und prozessualer / administrativer Ebene</li>
	<li style="list-style-position: inside;">Identifizierung von Wachstumschancen</li>
	<li style="list-style-position: inside;">Kontinuierliches Reporting und Auswertung der Ergebnisse</li>
</ul>

Qualifikation:

<ul>
	<li style="list-style-position: inside;">Qualifizierung als "Pharmareferent)</li>
	<li style="list-style-position: inside;">Hohe Affinität/Begeisterung für die Vermarktung hochwissenschaftlicher und technologisch fortschrittlicher medizinischer Produkte</li>
	<li style="list-style-position: inside;">Fähigkeit zu Gesprächen auf Augenhöhe mit Chirurgen (Hand, Trauma, Orthopädie) Verkaufserfahrung</li>
	<li style="list-style-position: inside;">Gutes Verständnis von Operationssälen und der Arbeitsumgebung von Chirurgen</li>
	<li style="list-style-position: inside;">Fähigkeit, komplexe klinische Studien zu verstehen und als Verkaufsinstrument zu nutzen</li>
	<li style="list-style-position: inside;">Fließende Beherrschung der deutschen und englischen Sprache</li>
	<li style="list-style-position: inside;">Bereitschaft zu Reisen nach Bedarf</li>
	<li style="list-style-position: inside;">Verständnis NUB Verfahren / Einzelfallantrag ist von Vorteil</li>
</ul>

Anforderungen: 
Beginn: Januar/Februar 2023 
Dauer: 6 Monate+ 
Kapazität: tbd
</div>

Sales Agent Surgery

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt"><div>One of our pharmaceutical clients in Germany is currently seeking freelance support as: CQV Engineers (M/W/D) Qualification:<ul><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Ideally qualified Chemical/Mechanical/Biochemical/Biopharma Engineer, but this is not mandatory.</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Minimum 3-5 year experience working as&nbsp;C&amp;Q engineer</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Experience in cell culture biotech stainless steel is the basic</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Experience in field commissioning of black Utilities /clean Utilities&nbsp;/ process Equipment&nbsp;USP&nbsp;(e.g. bioreactors, Media Prep, Media Hold, Harvest),&nbsp;DSP&nbsp;(e.g. Buffer Prep, Buffer Hold, Chroma Skids, Process Stations) auxillaries (Autoclaves / part washers, clean benches, etc.)</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Preferred experience in commissioning using&nbsp;Siemens PCS7&nbsp;or similar&nbsp;automation&nbsp;packages.</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Preferred experience working on 2 or more&nbsp;Biopharmaceutical/Biotech/Pharmaceutical&nbsp;Projects (no packaging projects)</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Experience problem solving; Team players; Field knowledge, hands-on approach ( no managerial function) mandatory</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Experience in mentoring team members</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Energetic, positive, and proactive</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Not averse to work in a 6 day week scenario</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">English language mandatory, also German could be an advantage</li></ul> Key data: 
<ul><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Start: 01.02.2023</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">FTE: full-time on site</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Duration: 6-10 months</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Conditions: Daily Rate (+-9h)&nbsp;</li><li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Location: South of Germany</li></ul></div></div>

CQV Experts

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Pharma-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Digital Marketing Manager/Digital Native (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li style="box-sizing: border-box;">Strategische Planung, Umsetzung und Optimierung von Performance Kampagnen</li>
	<li style="box-sizing: border-box;">Mitgestaltung der eCommerce-Strategie in Zusammenarbeit mit externen Partnern&nbsp;</li>
	<li style="box-sizing: border-box;">Steuerung von Social Media Kampagnen(Facebook/Instagram)</li>
	<li style="box-sizing: border-box;">Nutzung von Online-Tools wie Google Ads Editor oder Amazon Seller Central und Beherrschung von Digital Analytics-Themen</li>
	<li style="box-sizing: border-box;">KPI-Überwachung und Erstellung von Reportings via Power BI.</li>
	<li style="box-sizing: border-box;">Konzeption und Umsetzung von Digital Marketing Kampagnen wie Tracking, Influencer-Marketing oder den Aufbau eines TikToK-Accounts.</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li style="box-sizing: border-box;">Mehrjährige Berufserfahrung im Bereich SEA, Paid Social Ads und Amazon PPC.</li>
	<li style="box-sizing: border-box;">Gute Kenntnisse in Web Design und vorhandene Erfahrung im Aufbau eines eCommerce-Shop&nbsp;</li>
	<li style="box-sizing: border-box;">Idealerweise Pharmaerfahrung&nbsp;</li>
	<li style="box-sizing: border-box;">“Growth-Mindset” und die Fähigkeit Dinge voranzutreiben&nbsp;</li>
	<li style="box-sizing: border-box;">Fließende Deutsch-&nbsp; und Englisch-Kenntnisse</li>
</ul>

Rahmendaten: 
Start: asap, spätestens zum 15.10.2022 
Dauer: 6 Monate 
Auslastung: mind. 30 Stunden/Woche, Vollzeit präferiert 
Einsatzort: remote, gelegentlich Vorort&nbsp;

&nbsp;

&nbsp;
</div>

Digital Marketing Manager (m/w/d)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp;

Scrum Master (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li style="vertical-align:middle">Verantwortung für bis zu zwei interdisziplinäre agile Teams </li>
	<li style="vertical-align:middle">Unterstützung der Teams, sich kontinuierlich zu verbessern, um eigenverantwortlich die Erreichung der Unternehmensziele voranzutreiben</li>
	<li style="vertical-align:middle">Nutzung agiler Methoden (beispielsweise Scrum, Lean und Kanban), um Verbesserungen voranzutreiben</li>
	<li style="vertical-align:middle">Enge Zusammenarbeit mit den Product Ownern, anderen internationalen Teams und deren Scrum Mastern sowie dem Release Train Engineer&nbsp;</li>
	<li style="vertical-align:middle">Organisation von Team- und Programmevents wie Sprint / Increment Planning, Review, Retrospective und Backlog Refinement</li>
	<li style="vertical-align:middle">Erkennung von potenziellen Hindernissen in den agilen Teams und deren Lösung unter Einbeziehung aller Stakeholder&nbsp;</li>
	<li style="vertical-align:middle">Ansprechpartner für alle Fragen agiler Softwareentwicklung für die agilen Teams und Impulsgeber für die Weiterentwicklung agiler Prozesse&nbsp;</li>
</ul>

&nbsp;

&nbsp;Qualifikation:

<ul>
	<li style="vertical-align:middle">Studium der Informatik, einer anderen Ingenieurswissenschaft oder vergleichbare Qualifikationen</li>
	<li style="vertical-align:middle">mehrjährige Erfahrung als Scrum Master in der Softwareentwicklung, idealerweise in komplexen Umgebungen mit mehreren agilen Teams und in Kombination mit System- / Hardwareentwicklung.</li>
	<li style="vertical-align:middle">Azure DevOps, Jira oder vergleichbare Tools&nbsp;</li>
	<li style="vertical-align:middle">gute Methodenkenntnisse und entsprechende Zertifizierung z.B. als Certified Scrum Professional, Certified Scrum Master oder Certified Team Coach</li>
	<li style="vertical-align:middle">Gute Deutsch- und Englischkenntnisse</li>
</ul>

&nbsp;

Rahmendaten: 
Start: 01.08.2022 / flexibel 
Dauer: 24 Monate 
Auslastung: 4-5 Tage / Woche 
Einsatzort: vor Ort&nbsp;

&nbsp;
</div>

Scrum Master

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div>Einer unserer Pharma-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
 
Clinical Research Associate Deutschland / Onkologie (M/F/D) 
 
Aufgaben:
<ul>
	<li style="margin-top:20px; margin-left:45px;list-style-position:inside">Klinisches Monitoring bei aktuellen Studien (Phase 2-3) </li>
	<li style="margin-left:45px;list-style-position:inside">Studien Vorbereitung / Study Start up </li>
	<li style="margin-left:45px;list-style-position:inside">Qualification &amp; Initiation Visits </li>
	<li style="margin-left:45px;list-style-position:inside">Einreichungsprozesse (Vorbereitung Ethikeinreichungen) </li>
	<li style="margin-left:45px;list-style-position:inside">Betreuung der Studien </li>
	<li style="margin-bottom:20px; margin-left:45px;list-style-position:inside">Erstellung von Studiendokumenten </li>
</ul>
 
Qualifikation:

<ul>
	<li style="margin-top:20px; margin-left:45px;list-style-position:inside">Erfolgreich abgeschlossenes Naturwissenschaftliches Studium </li>
	<li style="margin-left:45px;list-style-position:inside">Mehrjährige CRA Erfahrung </li>
	<li style="margin-left:45px;list-style-position:inside">Erfahung mit Risk- based Monitoring (RBM) </li>
	<li style="margin-left:45px;list-style-position:inside">Erfahrung im Bereich Onkologie </li>
	<li style="margin-left:45px;list-style-position:inside">Hands-on Mentalität, Lösungsorientiert </li>
	<li style="margin-left:45px;list-style-position:inside">Reisebereitschaft DE </li>
	<li style="margin-bottom:20px; margin-left:45px;list-style-position:inside">Verhandlungssicher in Deutsch &amp; Englisch </li>
</ul>
 
Rahmendaten: 

<ul>
	<li style="margin-top:20px; margin-left:45px;list-style-position:inside">Start: asap, latest October 2022</li>
	<li style="margin-left:45px;list-style-position:inside">Dauer: 12 Monate plus </li>
	<li style="margin-left:45px;list-style-position:inside">Auslastung: 20-25 Stunden pro Woche remote</li>
</ul>
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CRA Onkologie

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Medizintechnik-Kunden im Großraum Aachen&nbsp;sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Prozessingenieur (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Optimierung bestehender Produktionsprozesse hinsichtlich Effizienz&nbsp;und Effektivität</li>
	<li>Prozesskontrolle, Fehleranalyse und Umsetzung von Lösungen</li>
	<li>CAPA Management</li>
	<li>Weiterentwicklung der Fertigungstechnik</li>
	<li>Prototypenbau, Erstmusterung und Dokumentationserstellung</li>
	<li>Erstellung von Change-Anträgen</li>
	<li>Überführung von Baugruppen und Produkten aus der Entwicklung in&nbsp;die Serienfertigung</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li>Erfolgreich abgeschlossenes Studium im Bereich Technik, Naturwissenschaften oder eine vergleichbare Qualifikation</li>
	<li>Mehrjährige Berufserfahrung im industriellen Produktionsumfeld, vorzugsweise in der Medizintechnik</li>
	<li>Sehr gutes analytisches Denkvermögen mit einem starken Willen zur Optimierung von Prozessen und der Fähigkeit, komplexe Sachverhalte einfach darzustellen und zu kommunizieren</li>
	<li>Eigenmotivierte, selbstständige, strukturierte, zielorientierte&nbsp;Arbeitsweise</li>
	<li>Konversationssichere Englischkenntnisse in Wort und Schrift</li>
</ul>

Rahmendaten: 
Start: asap 
Dauer: 6 Monate+ 
Auslastung: 4-5 Tage die Woche 
Einsatzort: Großraum Aachen

&nbsp;

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