Site Qa Head Csl Seqirus Amsterdam, Eu Qualified Person & Rp

CSL Ltd

Amsterdam, Netherlands
Not specified; not specified; benefits available
Not specified (assumed to be hybrid or onsite based on the nature of the role).
Eu qualified person eligibility
Responsible person duties execution
Cgmp compliance expertise
CSL Seqirus is seeking a Site Quality Head based in Amsterdam to lead the Quality Assurance and Site Quality teams, ensuring compliance with regulatory standards and fostering a strong quality culture. The ideal candidate will have significant experience in quality assurance, particularly within the pharmaceutical industry, and possess strong leadership and communication skills

Job Summary

  • The role provides strategic direction to the site quality organization while ensuring regulatory compliance of all GMP functions.
  • As a senior Qualified Person and Responsible Person, the incumbent is accountable for executing EU requirements for testing and release facilities.
  • CSL Seqirus is committed to attracting world-class employees with a core mission focused on inclusion, belonging, and pandemic preparedness.

Matching Summary

Match Score: 85

CSL Seqirus is seeking a Site Quality Head based in Amsterdam to lead the Quality Assurance and Site Quality teams, ensuring compliance with regulatory standards and fostering a strong quality culture. The ideal candidate will have significant experience in quality assurance, particularly within the pharmaceutical industry, and possess strong leadership and communication skills.

Salary

Not specified; Not specified; Benefits available

Skills & Requirements

Must-have

  • EU Qualified Person eligibility
  • Responsible Person duties execution
  • cGMP compliance expertise
  • Vaccines and Steriles experience
  • Regulatory inspection leadership
  • Risk-based decision making

Nice-to-have

  • Leadership in cross-functional teams
  • Process automation initiatives
  • Continuous improvement strategies
  • Strong communication skills
  • Inclusion and belonging culture

Key Requirements

  • Degree in life science meeting EU QP eligibility
  • Minimum 2 years management/leadership QA role
  • Minimum 5 years cGMP experience
  • Fluency in English required
  • Substantial industry experience in vaccines or biologicals

Work Rights

Not specified

Tailored Resume

Cover Letter