Manager Quality – International & Distribution Quality (idq)

Amgen

Breda, Netherlands
Competitive salary; bonus structure included; fixe...
Good distribution practice (gdp) knowledge
Good manufacturing practice (gmp) expertise
European pharmaceutical legislation understanding
The role provides Quality leadership and oversight across IDQ operations to ensure compliant distribution of pharmaceutical products in line with Good Distribution Practices across the EMEA region

Job Summary

  • The role provides Quality leadership and oversight across IDQ operations to ensure compliant distribution of pharmaceutical products in line with Good Distribution Practices across the EMEA region.
  • As a key team member, you will act as the Responsible Person or backup, maintaining full regulatory compliance and reporting quality matters to senior management.
  • Amgen offers a diverse and inclusive community where teammates are empowered to bring ideas to the table, along with competitive rewards including a fixed 13th month and collective health insurance.

Matching Summary

The role provides Quality leadership and oversight across IDQ operations to ensure compliant distribution of pharmaceutical products in line with Good Distribution Practices across the EMEA region.

Salary

Competitive salary; Bonus structure included; Fixed 13th month, holiday allowance, and collective health insurance

Skills & Requirements

Must-have

  • Good Distribution Practice (GDP) knowledge
  • Good Manufacturing Practice (GMP) expertise
  • European Pharmaceutical legislation understanding
  • Quality Management System (QMS) experience
  • Responsible Person (RP) or backup capability
  • Supply Chain Quality record management

Nice-to-have

  • Experience in complex matrixed environments
  • Strong cross-functional collaboration skills
  • Ability to drive continuous improvement programs
  • Fluency in English language
  • High attention to detail and accuracy

Key Requirements

  • Life Sciences degree or related discipline
  • Relevant experience in Quality and/or Supply Chain within regulated pharmaceutical environment
  • In-depth knowledge of Falsified Medicines Directive
  • Experience working with ERP systems and Microsoft Office

Work Rights

Not specified

Tailored Resume

Cover Letter