レベル: Entry level

ジョブタイプ: Full-time

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仕事内容

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 47,000 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 CDMOis one of the leading CDMOs in Europe providing high-quality, customized drug development solutions for specialty and biopharma clients. Our focus is to support clients on the earliest phases of their development pathway (from API to the clinical packaging).

Its Belgian subsidiary, Eurofins Amatsigroup NV, is based in Ghent, offering a complete drug development package for new drug entities (biological and chemical) up to early clinical phases to third parties to help them in speeding up the development and manufacturing of their drugs.

Job Description

He/She will support and collaborate with the upstream and downstream teams by preparing the buffers needed in their processes, and this for development and for cGMP purposes. Volumes ranging from some liters to up to 200 L.

He/She will also prepare the buffers needed for clients.

Preparations of buffers will be the main task. He/She will also be involved in the monitoring program (for air and water) and will be the back-up person for the monitoring activities.

His/her Main Responsibilities Are
  • Prepare buffers in a cGMP and non-GMP environment according to the applicable requirements as described in the companies quality procedures
  • Document the work performed in the applicable records
  • Play an active role in the housekeeping of the equipment and labs used
  • Play an active role in the tracking of stock of critical raw materials and disposables
  • Play an active role in the preparation of the tools needed for the productions of buffers (eg sterilisation of tubing, preparation of filters, ….)
  • Participate in activities to support the functioning of the team
His/her Back-up Activities Are
  • Perform the monitoring activities (HVAC, PW and MQ) according the applicable requirements as described in the companies quality procedures
  • Provide the monitoring data on time
  • Perform the housekeeping of the warehouse
  • Take samples of raw materials for incoming QC
Qualifications
  • A technical degree (A2 or Bachelor), preferably in life sciences or chemistry or pharmacy or other related degree
  • Possess knowledge of buffer preparations
  • Ability to work very accurate
  • Be flexible and communicative
  • Ability to evaluate performed activities and be able to think about and suggest changes/improvements in the manipulations
  • Ability to work independently as well as a member of a team in a dynamic environment
  • Having a technical feeling to work with more complex equipment
  • English (at least reading) and Dutch
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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締切: 10-01-2026

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