Quality Management Associate; M​/F​/D

Responsibilities

• Processing and evaluating incoming change requests (change control), as well as coordinating and tracking approved actions
• Processing incoming deviation reports and conducting or coordinating root cause analyses
• Defining and monitoring CAPA measures in collaboration with the relevant departments
• Supporting the relevant departments in preparing risk analyses, as well as tracking and verifying the effectiveness of risk‑mitigation measures
• Assisting in the qualification of suppliers, service providers, and materials to be used
• Supporting the preparation, execution, and follow‑up of regulatory and customer audits
• Compliance with regulatory and customer‑specific requirements in a GMP‑regulated environment
• Handling general departmental tasks in the area of quality management/quality assurance
• Planning and conducting employee training sessions

• Degree in a science or technical field (e.g., chemistry, pharmaceuticals, biology) with experience in a quality‑related environment
• Professional experience in quality management and/or quality assurance, ideally in the pharmaceutical, biotech, or related industries
• Proficiency in handling nonconformities, CAPA, and change control
• Desirable:
  Experience in supplier qualification, as well as audit preparation and execution
• Basic knowledge of peptide chemistry
• Good knowledge of GMP regulations (e.g., EU‑GMP, ICH) is an advantage
• Experience in risk management
• Very good German and English language skills
• Structured, meticulous, and independent work style
• Strong analytical thinking, problem‑solving skills, communication skills, and the ability to work in a team
• High reliability, sense of responsibility, and clear focus on quality

• A permanent position
• A pleasant work environment in a dynamic team
• A challenging role with a high degree of autonomy
• Professional development opportunities
• Regular company events
• A family‑friendly and growing company