CQV Engineer

France  ‐ Onsite

Keywords

Good Manufacturing Practices Cell Cultures Biotechnology Customer Relationship Management Filtration Regulatory Compliance Databases Consulting Project Planning French Recruitment Iq/oq/pq IT Recruitment Pharmaceutical Production

Description

We are working with a leading biopharmaceutical company who are seeking experienced CQV Engineers to support their expanding projects in upstream and downstream processes.

Key Responsibilities:
  • Lead IQ, OQ, and PQ activities for upstream (e.g., fermentation, cell culture) and downstream (e.g., filtration, purification) processes.
  • Prepare and review CQV documentation (protocols, reports, SOPs).
  • Ensure compliance with cGMP, FDA, and EMA regulations.
  • Collaborate with cross-functional teams and manage project timelines.


Requirements:
  • Bachelor's degree in Engineering, Biotechnology, or related field.
  • 3-5 years' experience in CQV within biopharma or pharmaceutical manufacturing.
  • Expertise in upstream and downstream processes and IQ/OQ/PQ protocols.
  • Strong understanding of cGMP, FDA, and EMA standards.
  • French speaking is considered a plus.


Darwin Recruitment AG is a Zurich based, SECO licensed, privately owned subsidiary of Darwin Professional Staffing Group Ltd (a Global IT Recruitment Consultancy).

Darwin Recruitment AG manages client relationships whilst also utilising Darwin Professional Staffing Group databases and networks to source Candidates and fulfil client requests.

We do not ask for a placement fee from Candidates/Employees.

If you wish to contact a specialist regarding this role, or your job search in general, please contact
Start date
10.2024
Duration
6 months
(extension possible)
From
Darwin Recruitment
Published at
17.09.2024
Contact person:
Greg King
Project ID:
2796784
Industry
Medicine and Pharmaceuticals
Contract type
Freelance
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