
Senior Validation Engineer
1 week ago
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PM Group is looking to expand the CQV team. This role will be supporting one of our pharmaceutical clients in the field of commissioning, qualification and validation work.
:
- Generation and execution of validation protocols and reports (including IQs, OQs, PQs, QAPs, etc.).
- Working as a seconded PM Group resource in a client-led team.
- To lead and/or support validation projects and activities on site, as directed and as appropriate.
- To prepare validation plans in line with the strategic goals of the client and to manage timely and compliant delivery of the plan.
- Commissioning and validation of various new technologies and new equipment.
- To develop and execute Commissioning & Qualification lifecycle protocols as per the specific project requirements.
- Leading and supporting SATs.
- Supporting and representing the technical quality team in meetings, visits, troubleshooting exercises, and audits.
- Ensuring manufacturing equipment is qualified in line with production schedule requirements.
- Developing and writing validation procedures according to cGMP and regulatory requirements.
- Generating and executing validation documentation.
- Providing continuous improvement for existing validation procedures.
- Data collation and analysis via sophisticated computer software.
:
**Qualifications & Requirements**
- Applicants will have experience of equipment validation on multiple projects in the pharmaceutical and/or biopharmaceutical sectors.
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