USP Specialist - Manufacturing - Biotech
We offer you a new opportunity as USP Specialist for a global biopharmaceutical company.
Our client is a leading European pharmaceutical CDMO focused on healthcare biotechnology, with a focus on process development and cGMP manufacturing of biological products, and cell therapy. They are continuously growing and are looking for a QA Manager with experience in biologics and biotech and with a desire to grow and perform innovative projects.
* +2 years experience in R&D or Manufacturing in USP processes, within the bio pharmaceutical industry or the academic field.
* Knowledge of USP techniques for proteins.
* Knowledge of biochemical and structure of proteins.
* Experience in GMP environment is a nice to have.
* Experience in the preparation and review of documentation (SOPs, Development Reports, Validation Reports, protocol) in English to regulatory standards.
* Fluent English - Spanish is a nice to have.
What is offered:
- Immediate incorporation in a young and growing working environment.
- Growth opportunities.
- Location: North of Spain
Do not hesitate to contact us and send your CV in word format to email@example.com to receive all the information and apply to the offer.
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