Description
Validation EngineerOur global pharmaceutical client is currently undergoing a site-wide substantial transformation program, changing from production of chemicals to production of a range of biopharmaceutical products.
They are currently preparing to receive the new products and start production, and they have reached validation stages.
To support the engineering team the client is looking for a number of experienced Validation Engineers with a strong biopharmaceutical background.
Location: Paris
Duration: 4 months
Role :
- Support the site in its transition to biopharmaceutical manufacturing by providing technical expertise on validation of new biopharmaceutical equipment.
- Completion of validation documentation including IQ/OQ/PQ.
- Equipment will include (upstream and downstream): reactors, fermenters, homogenizers, filtration units, chromatography columns and centrifuges.
Requirements:
- Engineering degree or equivalent experience in an engineering function in a regulated environment.
- Biopharmaceutical upstream and downstream equipment validation experience.
- Previous experience of writing and executing validation documentation.
- Knowledge of GMP and FDA requirements.
- Experience working to tight project schedules and deadlines.
- Both a strong team player and able to work independently.
- French language capabilities must be fluent.