CQV Engineer

Visp  ‐ Onsite

Keywords

Auditing Biology Good Manufacturing Practices Regulatory Compliance Databases Engineering Quality Management

Description

We are seeking an experienced CQV Engineer to join our team on a contract basis, supporting a leading pharmaceutical manufacturing facility. The role will focus on clean utilities, HVAC, black utilities, and primarily performance qualification activities.

Key Responsibilities:
  • Execute CQV activities for clean utilities, HVAC, black utilities.
  • Develop and review validation documentation, including protocols (IQ/OQ/PQ).
  • Ensure compliance with cGMP, FDA, and EU regulations.
  • Perform risk assessments and troubleshoot validation issues.
  • Work closely with cross-functional teams to ensure project deliverables are met.
  • Support regulatory audits and inspections related to CQV.


Key Requirements:
  • Proven experience in CQV within pharmaceutical manufacturing.
  • Strong knowledge of clean utilities, HVAC, and black utilities.
  • Familiarity with GMP, FDA, and EU regulatory requirements.
  • Ability to write and execute IQ, OQ, and PQ protocols.
  • Strong problem-solving and communication skills.


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
3.2025
From
Darwin Recruitment
Published at
19.02.2025
Contact person:
Greg King
Project ID:
2850339
Industry
Medicine and Pharmaceuticals
Contract type
Freelance
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