Qa Associate - Qa Lab

Johnson & Johnson Johnson & Johnson · Pharma · Geel, Antwerp, Belgium

This role provides quality oversight for Quality Control (QC) laboratories in the pharmaceutical industry, ensuring compliance with cGMP, ICH guidelines, and regulatory expectations for testing of APIs, intermediates, raw materials, and packaging materials. Responsibilities include reviewing GMP documentation, supporting deviation investigations, overseeing analytical method transfers, and acting as a subject matter expert during inspections.

What you'd actually do

  1. Act as QA Point of Contact for QC laboratories, ensuring alignment with global regulations and internal standards
  2. Provide QA review and approval for GMP documentation supporting laboratory operations
  3. Support investigation of laboratory deviations, including:
  4. Provide QA oversight on analytical method transfers and implementation
  5. Ensure timely and compliant handling of quality records (deviations, CAPAs, change controls, method transfer documentation)

Skills

Required

  • Master’s degree in a scientific field (analytics, chemistry, biotechnology or equivalent experience)
  • Minimum 5 years of experience in QC and/or QA within the pharmaceutical, chemical or food industry
  • At least 4 years in an analytical environment
  • Strong knowledge of cGMP, ICH guidelines, and regulatory expectations
  • Proven ability to make risk-based, data-driven decisions
  • Strong analytical thinking and problem-solving skills
  • Experience with analytical troubleshooting and investigation processes
  • Proven ability to work independently, manage multiple priorities, and collaborate cross-functionally
  • Strong communication and stakeholder management skills
  • Fluent in Dutch and English

Nice to have

  • Compliance Management
  • Continuous Improvement
  • Data Analysis
  • Quality Control (QC)
  • Quality Management Systems (QMS)
  • Quality Standards

What the JD emphasized

  • cGMP
  • ICH guidelines
  • regulatory requirements