Job Description

Quality Manager – Pharma / Process Validation (m/f/d) – Contract until July 2026 with option to extendStart: Immediately or by agreementAn international pharmaceutical company is looking to strengthen its quality team with a motivated professional for a strategically important Quality Manager position (PPQ Drug Substance & Drug Product). This is a contract role until July 2026, with the possibility of extension.Your ResponsibilitiesTake full quality responsibility for the PPQ phase of drug substances and drug productsReview and approve all PPQ documentation and evaluate executed batch records and deviationsParticipate in FMEA and other risk-based analysesCollaborate closely with global CMC, Regulatory, MSAT, and QA teamsProvide regular status updates and manage escalations effectivelyYour ProfileMinimum 5 years of experience in Quality Management / Process Validation, ideally in pharmaStrong knowledge of GMP requirements for small molecule drug substances and drug productsAbility to oversee complex processes, manage priorities confidently, and take ownership of cross-functional interfacesIndependent, structured, and solution-oriented working styleIf you enjoy actively shaping quality, we look forward to your application!

Job Application Tips

  • Tailor your resume to highlight relevant experience for this position
  • Write a compelling cover letter that addresses the specific requirements
  • Research the company culture and values before applying
  • Prepare examples of your work that demonstrate your skills
  • Follow up on your application after a reasonable time period