Technical Services & Validation Specialist (m/f)

pfizer.de

Savski Marof, ,
Base: not specified; bonus/equity: christmas, east...
Hybrid
Technology transfer activities
Process validation for sterile injectables
Gmp and regulatory compliance
In this role, you will play an integral part in technology transfer, process validation, and lifecycle management of biotechnological drug product processes

Job Summary

  • In this role, you will play an integral part in technology transfer, process validation, and lifecycle management of biotechnological drug product processes.
  • You will work in an environment that encourages ownership, accountability, and continuous learning, balancing independent technical responsibility with strong cross-functional collaboration at site and global level.
  • Benefits include organized transport, strong education programs, bonuses, affordable meals, professional development, free psychotherapy and coaching sessions, and opportunities to work on projects with other Pfizer sites.

Matching Summary

In this role, you will play an integral part in technology transfer, process validation, and lifecycle management of biotechnological drug product processes.

Salary

Base: Not specified; Bonus/Equity: Christmas, Easter and holiday bonus; Benefits: Yearly pay increase, affordable meals, free psychotherapy and coaching sessions

Skills & Requirements

Must-have

  • Technology transfer activities
  • Process validation for sterile injectables
  • GMP and regulatory compliance
  • Cross-functional collaboration
  • Technical support to manufacturing
  • Process optimization initiatives

Nice-to-have

  • Hands-on drug product technology transfer
  • Experience with statistical tools
  • Digital quality systems experience
  • Strong digital skills
  • Analytical thinking and problem solving
  • Ownership and accountability mindset

Key Requirements

  • University degree in Pharmacy, Biotechnology, Chemical Engineering or related
  • 3 years experience in pharmaceutical technical services or process validation
  • Working knowledge of GMP and regulatory expectations
  • Proficiency in English and Croatian

Work Rights

Not specified

Tailored Resume

Cover Letter