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 Qualifications 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 Benefits 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 #J-18808-Ljbffr Intavis Peptide Services