CHEPLAPHARM Arzneimittel GmbH
Head of MSAT(m/w/x)
Vollzeitmit HomeofficeSenior
Greifswald, Berlin, Binningen
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CHCHEPLAPHARM Arzneimittel GmbH
Senior MSAT Manager(m/w/x)
Greifswald, Berlin, Binningen
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Leading technology transfers and on-site compliance assessments for established pharmaceutical brands. Master's degree and 5+ years in pharma/biotech MSAT or tech transfer required. Work from another EU country up to 2 months/year.
Anforderungen
- Master's degree in Pharmacy, Biotechnology, Life Sciences, Chemical Engineering, or related scientific discipline
- More than 5 years of relevant professional experience in pharmaceutical, biotechnology, or healthcare industry
- Experience ideally within MSAT, technology transfer, manufacturing, or technical operations
- Successful management of complex, long-term projects with multiple stakeholders, changing priorities, and cross-functional collaboration
- Strong technical expertise
- Enjoyment of analyzing complex challenges
- Enjoyment of evaluating alternative solutions
- Driving practical, sustainable outcomes
- Thorough understanding of GMP requirements
- Thorough understanding of pharmaceutical regulations
- Thorough understanding of industry best practices in international environment
- Confident engagement with stakeholders at all organizational levels
- Skills in influencing, negotiating, and building strong professional relationships
- Experience leading cross-functional teams and projects in a matrix environment
- Driving results through collaboration, influence, and expertise
- Taking ownership of responsibilities
- Making sound decisions
- Thriving in dynamic environments requiring flexibility and initiative
Aufgaben
- Lead complex technology transfer programs
- Ensure successful technical execution of projects
- Drive projects from planning to implementation
- Maintain highest quality standards
- Perform on-site technical compliance assessments
- Verify activities meet internal and regulatory standards
- Review and approve technical documentation
- Maintain accuracy and consistency in documentation
- Provide expert guidance on pharmaceutical and technological matters
- Support teams in navigating complex technical challenges
- Ensure adherence to international regulations and industry standards
- Contribute to successful delivery of compliant products and processes
- Evaluate and contribute to technical RFQs
- Provide expert input for business development
- Act as primary technical contact for external service providers
- Build strong partnerships with external providers
- Ensure successful project delivery with external providers
- Create and review GMP-relevant documentation
- Continuously improve GMP-relevant documents
- Coordinate cross-functional projects
- Align diverse stakeholders
- Ensure project milestones are achieved on time and in scope
Berufserfahrung
- 5 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Lockere Unternehmenskultur
- Diverse working environment
- Employees from 40 countries
Flexibles Arbeiten
- Flexible working models
- Work-life balance
- Working time account
Workation & Sabbatical
- Work from another EU country (up to 2 months/year)
Mehr Urlaubstage
- Compensatory time off
- 30 days of holiday
Sonstige Zulagen
- Flexible benefits budget
- Subsidies for meal costs
Betriebliche Altersvorsorge
- Company pension provision
Gesundheits- & Fitnessangebote
- Fitness offers
- Health offers
Öffi Tickets
- Subsidies for travel costs
Mitarbeiterrabatte
- Corporate benefits platform access
- Discounts at partner companies
Weiterbildungsangebote
- Internal training courses
- External training courses
Team Events & Ausflüge
- Company events
- Team events
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens CHEPLAPHARM Arzneimittel GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
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CHCHEPLAPHARM Arzneimittel GmbH
Senior MSAT Manager(m/w/x)
Greifswald, Berlin, Binningen
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Leading technology transfers and on-site compliance assessments for established pharmaceutical brands. Master's degree and 5+ years in pharma/biotech MSAT or tech transfer required. Work from another EU country up to 2 months/year.
Anforderungen
- Master's degree in Pharmacy, Biotechnology, Life Sciences, Chemical Engineering, or related scientific discipline
- More than 5 years of relevant professional experience in pharmaceutical, biotechnology, or healthcare industry
- Experience ideally within MSAT, technology transfer, manufacturing, or technical operations
- Successful management of complex, long-term projects with multiple stakeholders, changing priorities, and cross-functional collaboration
- Strong technical expertise
- Enjoyment of analyzing complex challenges
- Enjoyment of evaluating alternative solutions
- Driving practical, sustainable outcomes
- Thorough understanding of GMP requirements
- Thorough understanding of pharmaceutical regulations
- Thorough understanding of industry best practices in international environment
- Confident engagement with stakeholders at all organizational levels
- Skills in influencing, negotiating, and building strong professional relationships
- Experience leading cross-functional teams and projects in a matrix environment
- Driving results through collaboration, influence, and expertise
- Taking ownership of responsibilities
- Making sound decisions
- Thriving in dynamic environments requiring flexibility and initiative
Aufgaben
- Lead complex technology transfer programs
- Ensure successful technical execution of projects
- Drive projects from planning to implementation
- Maintain highest quality standards
- Perform on-site technical compliance assessments
- Verify activities meet internal and regulatory standards
- Review and approve technical documentation
- Maintain accuracy and consistency in documentation
- Provide expert guidance on pharmaceutical and technological matters
- Support teams in navigating complex technical challenges
- Ensure adherence to international regulations and industry standards
- Contribute to successful delivery of compliant products and processes
- Evaluate and contribute to technical RFQs
- Provide expert input for business development
- Act as primary technical contact for external service providers
- Build strong partnerships with external providers
- Ensure successful project delivery with external providers
- Create and review GMP-relevant documentation
- Continuously improve GMP-relevant documents
- Coordinate cross-functional projects
- Align diverse stakeholders
- Ensure project milestones are achieved on time and in scope
Berufserfahrung
- 5 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Lockere Unternehmenskultur
- Diverse working environment
- Employees from 40 countries
Flexibles Arbeiten
- Flexible working models
- Work-life balance
- Working time account
Workation & Sabbatical
- Work from another EU country (up to 2 months/year)
Mehr Urlaubstage
- Compensatory time off
- 30 days of holiday
Sonstige Zulagen
- Flexible benefits budget
- Subsidies for meal costs
Betriebliche Altersvorsorge
- Company pension provision
Gesundheits- & Fitnessangebote
- Fitness offers
- Health offers
Öffi Tickets
- Subsidies for travel costs
Mitarbeiterrabatte
- Corporate benefits platform access
- Discounts at partner companies
Weiterbildungsangebote
- Internal training courses
- External training courses
Team Events & Ausflüge
- Company events
- Team events
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens CHEPLAPHARM Arzneimittel GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
CHEPLAPHARM Arzneimittel GmbH
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen ist ein globales und wachsendes Specialty Pharmaunternehmen mit einem außergewöhnlichen, nachhaltigen Geschäftsmodell.
Noch nicht perfekt?
- CHEPLAPHARM Arzneimittel GmbH
Head of MSAT(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Senior Project Manager Technology Transfer(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin - CHEPLAPHARM Arzneimittel GmbH
(Senior) Specialist Supply Projects(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin - CHEPLAPHARM Arzneimittel GmbH
Senior Project Lead End to End Integration(m/w/x)
VollzeitRemoteSeniorGreifswald, Berlin - CHEPLAPHARM Arzneimittel GmbH
Global Head of Product Operations(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen