Aufgaben

  • Part of the Primary Packaging and Raw Material QC team, responsible for incoming goods control of raw materials to support drug product manufacturing
  • Review and report external lab results, assess against specifications and historical data
  • Evaluate testing requirements for raw materials per compendial and internal standards
  • Support lab investigations with external testing labs
  • Author and revise specification sheets and change management documentation
  • Compile, interpret, and present data
  • Write and approve reports and SOPs
  • Contribute to process improvements

Qualifikationen

  • Technician with 5+ years in the pharmaceutical industry (ideally raw materials) or Bachelor’s degree in Chemistry or related field with 2–3 years of industry experience
  • Understanding of cGMP, prior GMP experience preferred
  • Experience in analytical testing of raw materials desirable
  • Strong problem-solving, analytical, and communication skills
  • Proactive mindset