Senior Qa Associate Commercial

J&J FAMILY OF COMPANIES

Geel, Antwerp, Belgium
Not specified; not specified; competitive compensa...
Not specified (assumed to be hybrid based on the nature of the role and industry practices).
Master scientific degree in chemistry or pharmaceutical sciences
In-depth knowledge of cgmp and ich guidelines
Fluent in dutch and english spoken and written
Johnson & Johnson is seeking a Senior QA Associate Commercial in Geel, Belgium, to oversee the quality assurance of commercial Active Pharmaceutical Ingredients (APIs) within their Innovative Medicine Supply Chain. The role emphasizes compliance with regulations, collaboration with stakeholders, and fostering a quality culture within the organization

Job Summary

  • This role involves overseeing the quality assurance and timely release of commercial Active Pharmaceutical Ingredients (APIs) at the Geel site.
  • The successful candidate will act as a spokesperson during Health Authority inspections and customer audits while ensuring strict regulatory compliance.
  • Johnson & Johnson offers a competitive compensation package, tailored benefits, and an inclusive environment that empowers professionals to drive their careers.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior QA Associate Commercial in Geel, Belgium, to oversee the quality assurance of commercial Active Pharmaceutical Ingredients (APIs) within their Innovative Medicine Supply Chain. The role emphasizes compliance with regulations, collaboration with stakeholders, and fostering a quality culture within the organization.

Salary

Not specified; Not specified; Competitive compensation and benefits package mentioned

Skills & Requirements

Must-have

  • Master Scientific degree in chemistry or pharmaceutical sciences
  • In-depth knowledge of cGMP and ICH guidelines
  • Fluent in Dutch and English spoken and written
  • Experience with Quality Systems and regulatory inspections
  • Ability to work independently under time pressure

Nice-to-have

  • Experience as a release responsible in chemical supply chain
  • Strong coaching and training skills on cGMP requirements
  • Demonstrated ability to influence across organizational boundaries
  • Experience driving innovation and continuous improvement initiatives
  • Subject Matter Expertise in assigned quality processes

Key Requirements

  • Master Scientific degree (chemistry, pharmaceutical sciences, bioengineer)
  • Fluency in Dutch and English required
  • Experience in Chemical/Pharmaceutical Supply Chain or QA
  • Knowledge of regulatory inspections and preparedness

Work Rights

Not specified

Tailored Resume

Cover Letter