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Thermo Fisher Scientific in Groningen produces biopharmaceuticals for clinical trials and commercial use in a GMP environment. The role works in the USP department, within a cleanroom, handling thawing to 1000L/2000L bioreactors and collaborating with multiple teams to ensure compliant production.
The position emphasizes precision, safety, and cGMP/EH&S compliance, with opportunities to work cross-functionally across DSP, MBP, MSAT, and QA teams.
Make biopharmaceutical products following international quality standards set by the FDA, EMEA and ICH and other regulatory organizations. We follow strict rules to make sure everything is done safely adhering to the GMP-compliance regulations set by the regulatory organizations. Our work must be precise and efficient to protect the quality and value of our products.
On the Groningen site we produce medicines for clinical trials (phases I, II, and III) and commercial use using mammalian cell lines. This position is for the USP (Upstream Processing) department. In this department, you will be working in the cleanroom with cells and follow the process from thawing to bioreactors of 1000L/2000L.
At Thermo Fisher’s Groningen site, we manufacture a diverse range of products for both clinical trials and commercial use. This diversity means production tasks can vary from first-time production runs to routine commercial batch manufacturing. Given the variety of customers and products, processing steps also differ significantly. Due to the high value of our products and intermediates, accuracy, reliability, and compliance with cGMP and EH&S regulations are crucial. This job requires flexibility and teamwork. You’ll mostly work with the USP team, but sometimes you’ll collaborate with other departments such as the Down Stream (DSP), Media Buffer Preparation (MBP), Manufacturing Science and Technology (MSAT) and Quality Assurance (QA) teams.