Quality Management Specialist for Active Ingredients | QM Spezialist Wirkstoffe Vollzeit, befristet auf 24 (m/w/d)
Nordmark Pharma GmbH
Job Summary
As a Quality Management Specialist at Nordmark Pharma, you will play a critical role in ensuring 'Quality on the Floor' for biological and biotechnological active ingredients. Your day-to-day responsibilities include creating and maintaining standard operating procedures, defining key performance indicators (KPIs), and providing expert GMP coaching to production teams. You will maintain a strong presence on the shop floor, participating in shift handovers, conducting GMP walkthroughs, and reviewing batch documentation. Additionally, you will support the management of deviations, CAPAs, and change controls while assisting with audits and inspections. This position is ideal for a proactive professional who enjoys a mix of administrative oversight and hands-on process observation. Nordmark offers a highly attractive package including a salary based on the TV ChemieNord collective agreement, 30+ days of vacation, and a flexible 38.5-hour work week, all within an innovative, medium-sized company recognized as a top employer in the German pharmaceutical industry.
Required Skills
Education
Completed University degree (Diploma/Master/PhD) in Pharmacy, Biotechnology, or a related Natural Science field.
Experience
- Several years of professional experience in pharmaceutical manufacturing or quality control
- Proven experience in the application of risk management and root cause analysis methods
- Extensive experience working within a GMP-regulated environment
- Experience in creating, maintaining, and training on quality documentation
Languages
Additional
- This is a full-time position (38.5 hours/week) with a fixed-term contract of 24 months. The role is based in Uetersen, Germany and requires presence on the shop floor for process monitoring and shift handovers.
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