QA Manager GMP (m/w/d)

Eurofins is an international life science company that offers customers from various industries a unique range of analytics services to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the largest companies in the world to ensure that the delivered products are safe, their ingredients are authentic and the labelling is correct. The company is a leading global provider of analytics for food, environment, pharmaceutical and cosmetic products as well as agricultural research services (CRO). In addition, Eurofins is one of the world's independent market leaders for testing and laboratory services in the fields of genomics, pharmacology, forensics, CDMO (contracting and development), material sciences and support for clinical studies. In just 30 years, Eurofins has grown from a laboratory in Nantes, France, to approximately 61,000 employees in a network of more than 1000 independent companies in 62 countries with more than 900 laboratories. Eurofins offers a portfolio of more than 200,000 analytical methods to assess the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products as well as innovative services in the field of clinical diagnostics as one of the world's leading, emerging providers of specialized clinical diagnostic tests. In 2024, Eurofins achieved a total turnover of 6.515 billion euros and has been one of the shares with the best value development in Europe over the past 20 years. For the Eurofins BioPharma Product Testing Hamburg GmbH we are looking for a QA Manager GMP (m/w/d) for the Hamburg location at the next time in full time.

Maintaining and optimizing the GMP QA system and active cooperation in further development (e.g. processes, documents) Testing of the GMP Preparation, implementation and follow-up of internal and external audits/inspections Technical advice of the operational departments in all GMP matters Processing of deviations, changes, CAPA, OOS, complaints Planning, implementation and coordination of qualifications

Completed studies in the field of pharmacy, biology, chemistry or comparable completed vocational training (Chemie-/Biologielaborant/CTA/BTA/PTA or comparable) with several years of professional experience 1-2 years GMP professional experience in pharmaceutical industry (QA or QC) desirable Good understanding of the national and international GMP regulations regarding the implementation of GMP requirements in QC routine analysis Very good knowledge of German and English in word and writing Knowledge of project management is desirable Good MS Office and EDV knowledge Communication and team skills Fun at work, a high level of commitment and motivation

We offer Flat hierarchies with short decision paths

Varied activities in an attractive team

Development opportunities in an international company JOBV1_EN