Qualified Person

539

Haarlem, , Netherlands
Base: competitive salary; bonus/equity: incentive ...
Not specified
Batch documentation review
Quality oversight of supply chains
Compliance with gmp requirements
The company 539 is seeking a Qualified Person for their Haarlem location, responsible for overseeing quality throughout the supply chain and ensuring compliance with regulations for pharmaceutical products. The role offers opportunities for growth and emphasizes the importance of quality management in a collaborative international environment

Job Summary

  • The Qualified Person is responsible for quality oversight of the entire supply chain including batch certification for pharmaceutical products produced internally and by international CMOs.
  • The role involves leading batch documentation review, advising on compliance improvements, and approving production-related investigations within a multidisciplinary team.
  • The company offers a competitive salary, 35.5 vacation days, various bonuses, excellent pension, training modules, sport facilities, mental wellbeing support, and a high-quality onsite restaurant.

Matching Summary

Match Score: 85

The company 539 is seeking a Qualified Person for their Haarlem location, responsible for overseeing quality throughout the supply chain and ensuring compliance with regulations for pharmaceutical products. The role offers opportunities for growth and emphasizes the importance of quality management in a collaborative international environment.

Salary

Base: Competitive salary; Bonus/Equity: Incentive Plan, 8% vacation allowance, 3% year-end bonus; Benefits: Pension, training modules, sport facilities, mental wellbeing support

Skills & Requirements

Must-have

  • Batch documentation review
  • Quality oversight of supply chains
  • Compliance with GMP requirements
  • Quality release and product certification
  • Deviation investigations
  • Quality assurance processes
  • Manufacturing quality control

Nice-to-have

  • Proactive and decisive mindset
  • Strong communication skills in Dutch and English
  • Leading international investigations
  • Building cross-functional relationships
  • Quality policy development
  • Stress resistant personality

Key Requirements

  • WO degree in Biotechnology, (Micro-)Biology, Pharmacy with pharmacist diploma or equivalent
  • Several years experience as Qualified Person in pharmaceutical industry
  • Experience with EU and international regulations including EMEA, FDA, Anvisa
  • Experience with complex supply chain quality oversight
  • Excellent Dutch and English communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter