Qc Analyst

Il y a 2 mois

Gent, Belgique Eurofins Belgium BioPharma Services Temps plein

**Company Description**
Eurofins CDMO is a leading international Contract Development and Manufacturing Organization (CDMO) based in Europe. Our company focuses on drug product development and manufacturing for chemical/biological entities and drug substance development and manufacturing for biological entities. We support small and major biopharmaceutical companies in an innovative way to help them achieving their (pre)clinical milestones timely. Our facilities are perfectly designed for clinical and/or small scale commercial batches either for non-sterile or sterile dosage forms. With approximatively 350 staff, we operate out of 8 sites in France, Belgium and Italy.

Eurofins Amatsigroup wishes to expand its team with a **QC Analyst**. We are looking for a person that reports to the QC Manager of the Drug Product Business Unit.

**His/her main responsibilities are**:

- You follow up the quality of a variety of Drug Products used in clinical trials (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 assist in the validation of analytical methods to support the quality control testing of Drug Products.
- You accurately calculate, report, and review the analytical test results.
- You support preparation of the applicable protocols and reports.
- You support/coordinate the maintenance and calibration of the analytical equipment.

**Qualifications**
- You hold a professional bachelor degree with scientific orientation (biomedical laboratory technology, chemistry or pharmaceutical sciences) or other related education/experience.
- You have 3 years of relevant experience with our core analytical techniques such as chromatography (HPLC/UPLC - Empower CDS), dissolution and Karl Fischer.
- Bonus: you are familiar with functioning in a regulated environment (GLP/GMP).
- Recent graduates will also be considered
- You are punctual, well organized and 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 English (written and spoken), Dutch is an advantage.

**Additional Information**
- Day to day variety in projects and analyses;
- A wide range of new, state of the art, analytical techniques for you to master;
- Personal development through learning on the job from experienced team members and additional external trainings;
- A position with responsibility within a young and dynamic international pharmaceutical company, with room to grow;
- A market oriented compensation, including laptop, lunch vouchers, commuting fee, hospitalization insurance, pension fund;
- 32 holidays, with additional loyalty days;
- Regular team activities organized by our EuroFun team.

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