CQV Engineer
Process Engineering Specialists
Posted
last week
Singapore
Onsite
SGD 6K
Mid Level
Full Time
Sema Summary
Process Engineering Specialists seek a CQV Engineer to manage validation projects in the pharmaceutical sector. The role requires a focus on quality outcomes and strong communication with clients.
About Company
Process Engineering Specialists is an international services company that provides project management and automation services in pharmaceuticals and related sectors. They focus on delivering high-quality results for their clients worldwide.
Core Requirements
- Bachelor's degree in Engineering or related field.
- 4-7 years of experience in validation/CQV.
- Strong understanding of pharmaceutical facilities.
- Experience in protocol development (IQ, OQ, PQ).
- Ability to manage validation projects effectively.
Responsibilities
- Lead commissioning, qualification, and validation of facilities.
- Develop and review validation protocols.
- Interface with clients and vendors.
- Manage all facets of validation projects.
- Maintain strong communication with client representatives.
- Use process automation systems for validation tasks.
- Ensure compliance with industry standards.
Must Have skills
Job Keywords
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