Senior Process Validation Specialist

vor 2 Wochen


Wien, Österreich Haybury Vollzeit

Do you have a passion for Biopharmaceutical Manufacturing Processes and Validation?

We are working with a leading global pharmaceutical company with a significant number of first in class and medical breakthrough pipeline projects, to identify a senior level professional who can support the validation of biopharmaceutical manufacturing processes in order to ensure timely market submission of a biopharmaceutical product.

You will be responsible for the following tasks:

- Preparation and creation of independent validation reports in English: Preparation of Process Performance Qualification (PPQ) reports for both upstream and downstream biopharmaceutical manufacturing processes, as well as Lifetime (resin/membrane reuse) and Process Intermediate Hold Time Reports
- Technical assessment of the continued use of chromatography gels and Tangential Flow Filtration (TFF) membranes

You will bring to the role:

- Deep understanding of process validation and experience in managing process engineers
- Fluency in English and Germany

Contact Luke at +44 1273 059 669

Luke is a Senior Consultant at Haybury Search covering Europe, UK, North America and Asia.

pharmaceuticalmanufacturing #ProcessEngineering #ProcessValidation #GMP #RegulatoryAffairs #RegulatorySpecialist #Reg #Upstream #Downstream #Process Development

**Job Type**: Contract
Contract length: 18 months



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