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CHCHEPLAPHARM Arzneimittel GmbH

Head of MSAT(m/w/x)

Greifswald, Berlin, Binningen
Vollzeitmit HomeofficeSenior
Jetzt bewerben

Leading global MSAT operations for specialty pharmaceuticals, driving operational excellence and site alignment. Master's degree and 10+ years in pharma manufacturing or process development 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 10 years of professional experience in pharmaceutical industry (MSAT, manufacturing, technology transfer, process development, or related technical functions)
  • More than 10 years of successful team leadership experience
  • Strong ability to motivate, develop, and empower employees
  • Thorough understanding of global pharmaceutical regulations
  • Thorough understanding of GMP requirements
  • Thorough understanding of industry best practices
  • Excellent relationship building skills with stakeholders
  • Confident influencing and collaborating across functions, sites, and cultures
  • Skilled in evaluating complex business and technical challenges
  • Skilled in assessing alternative solutions
  • Skilled in identifying effective paths forward
  • Strong decision-making capabilities
  • Ability to balance strategic priorities with operational needs
  • Enjoyment of working in a global environment
  • Comfortable collaborating with international teams and stakeholders

Aufgaben

  • Lead global MSAT operations
  • Drive operational excellence
  • Ensure project and site alignment
  • Provide disciplinary and functional leadership
  • Foster a collaborative environment
  • Support team growth and performance
  • Execute technology transfer projects
  • Guide initial planning to commercial readiness
  • Conduct on-site technical compliance assessments
  • Ensure internal and regulatory compliance
  • Review and approve technical documentation
  • Authorize product and process transfer documents
  • Serve as a trusted technical advisor
  • Support pharmaceutical and technological questions
  • Manage technical RFQ components
  • Provide expert assessments for business decisions
  • Coordinate with external service providers
  • Ensure high-quality collaboration and delivery

Berufserfahrung

  • 10 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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