I am delighted to support a leading and reputable pharmaceutical company in their search for an experienced CQV engineer for a 12 month contract position.
- Preparation of documents associated with lifecycle of C&Q activities
- Preparation of protocols
- IQ / OQ
- Preparation, execution and follow-up of Design Review (DR) and Design Qualification (DQ) protocol
- Installation Verification execution
- System Startup activities
- Functional Testing of systems
- Change Management activities during project lifecycle
- Summary Report writing
- Contractors and/or Vendors coordination
Skills & Experience
- Minimum 3+ years experience in a CQV role.
- Hands on expertise required within a pharma or med device environment
- Experience with Regulatory and industry standards for GMP
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
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