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Commissioning, Qualification and Validation
2 weeks ago
**Process Engineering Specialists** **is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.
With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our multinational clients.
This focus, and our people's experience in delivering consistent quality results for our clients over the past 20 years has been key to our success to date.
We are currently looking for **Commissioning, Qualification and Validation [CQV] Lead **to join us on a permanent basis to help us deliver various projects in the Life Sciences Industry.
**What we’re looking for**:
- Develop the overall project C&Q plan/schedule, estimate the resources required, identify key roles and responsibilities and plan for C&Q staff on-boarding.
- Lead the generation of C&Q SOPs and validation documentation which include Validation Master Plan (VMP), System Level Impact Assessment (SLIA), User Requirement Specification (URS), Qualification Protocols (DQ, IQ and OQ) and traceability matrix for the project.
- Use Process Automation System for the commissioning and validation of process equipment.
- Interface with client personnel and outside vendors when necessary.
- Manage the overall CQ&V of facilities, utilities and equipment.
- Manage all facets of assigned validation projects while maintaining strong communication with client representatives on project status and assistance needed.
- Knowledge on Kneat/E-Val is preferred.
- German language proficiency is preferred.
