Technical Services & Validation Specialist (m/f)

Pf Health

Savski Marof, Croatia
Hybrid
Technology transfer
Process validation
Biopharmaceutical manufacturing
You will play an integral part in technology transfer, process validation, and lifecycle management of biotechnological drug product processes

Job Summary

  • You will play an integral part in technology transfer, process validation, and lifecycle management of biotechnological drug product processes.
  • Key responsibilities include leading and supporting technology transfer and process validation activities for biopharmaceutical drug product manufacturing, and preparing technical, validation, and regulatory documentation.
  • Pfizer offers a supportive environment with opportunities for career enhancement, professional development, and a strong education program.

Matching Summary

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

Skills & Requirements

Must-have

  • technology transfer
  • process validation
  • biopharmaceutical manufacturing
  • GMP compliance
  • English and Croatian proficiency

Nice-to-have

  • ownership and accountability
  • analytical thinking
  • problem-solving mindset
  • dynamic manufacturing environment
  • cross-functional collaboration

Key Requirements

  • University degree (VSS / 300 ECTS)
  • 3 years of working experience
  • Working knowledge of GMP
  • Scientific understanding of process engineering
  • Strong digital skills

Work Rights

Not specified

Tailored Resume

Cover Letter