USP Specialist - Manufacturing - Biotech

Oct 12, 2020
Nov 11, 2020
Irene Segura
Organization Type
Contract Type
Full Time

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 to receive all the information and apply to the offer.

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