QC Analyst

  • Full-time

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, 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 biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 50,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.

In 2021, Eurofins generated total revenues of EUR € 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins CDMO is a leading international Contract Development and Manufacturing Organization (CDMO) based in Europe. Our company focuses on drug product development for chemical/biological entities and drug substance development for biologics. We support small and major biopharmaceutical companies in an innovative way to help them achieving their (pre)clinical milestones timely. Our solid track record in developing and manufacturing New Biological Entities (NBE)/New Chemical Entities (NCE) is one of our strongest asset. Our facilities are perfectly designed for small clinical and/or commercial batches either for sterile or non-sterile dosage forms. With approximatively 400 staff, we operate out of 10 sites either in France or Belgium.

Job Description

  • You follow up the quality of a variety of Drug Products during Release and ICH stability studies (capsules, tablets, solutions, suspensions, injectables, biologics).
  • You perform Quality Control analyses using validated methods and pharmacopoeial procedures, in compliance with the GMP principles and the Quality Management System.
  • You accurately calculate, report, and review the analytical test results.
  • You support preparation of the applicable protocols and reports.
  • You support the set-up of deviations and investigations
  • You support the maintenance, calibration and qualification of the analytical equipment.
  • You support in the validation of analytical methods needed for the quality control and release of Drug Products.


  • You hold a professional Bachelor degree in biomedical laboratory technology, chemistry or pharmaceutical sciences.
  • You have 2 years of relevant professional experience with core analytical techniques such as chromatography (HPLC/UPLC - Empower CDS), dissolution and Karl Fischer.
  • You have experience in a regulated quality control environment (GMP).
  • You are punctual, well organized and are able to work independently after a training in matters entrusted to you.
  • You have a pro-active analytical, problem-solving mindset.
  • You are fluent in Dutch and English (written and spoken).

Additional Information

  • Work in a fast growing organization.
  • A position with responsibility within a dynamic company.
  • Personal development through learning on the job and additional external trainings.
  • A market oriented compensation.
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