Technical Services & Validation Specialist (m/f)

pfizer.ca

Savski Marof, Croatia
Hybrid
Technology transfer
Process validation
Lifecycle management
Lead and support technology transfer and process validation activities for biopharmaceutical drug product manufacturing (sterile injectables)

Job Summary

  • Lead and support technology transfer and process validation activities for biopharmaceutical drug product manufacturing (sterile injectables).
  • Prepare and maintain technical, validation, and regulatory documentation in compliance with GMP and regulatory requirements.
  • Work with modern automated systems, receive a strong education program, and have opportunities for career enhancement and development.

Matching Summary

Lead and support technology transfer and process validation activities for biopharmaceutical drug product manufacturing (sterile injectables).

Skills & Requirements

Must-have

  • technology transfer
  • process validation
  • lifecycle management
  • biopharmaceutical drug product manufacturing
  • GMP and regulatory requirements
  • English and Croatian proficiency

Nice-to-have

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

Key Requirements

  • University degree (VSS / 300 ECTS)
  • 3 years of working experience
  • Working knowledge of GMP
  • Proficiency in English and Croatian
  • Strong digital skills

Work Rights

Not specified

Tailored Resume

Cover Letter