Senior CQV Validation Engineer for Pharma

A leading company in temperature mapping solutions in Singapore is seeking a qualified professional to plan and execute temperature mapping studies and ensure validation compliance within GMP environments. Key responsibilities include performing CQV and supporting documentation for regulatory compliance. The ideal candidate holds a degree in Engineering or...

A leading life sciences firm in Singapore seeks a member for its MSAT team to ensure efficient execution of commissioning, qualification, and validation (CQV) activities. The ideal candidate will hold a degree in Engineering or Science and possess 1-3 years of relevant experience in the pharmaceutical sector. Strong knowledge of GxP regulations and excellent...

**Responsibilities**: - Lead a team of engineers in the delivery of commissioning activities/ qualification activities/automation I/O checks on all associated equipment to ensure CQV execution phases progress as per schedule. - Review of Commissioning, Qualification Verification (CQV) documentation Loops packs for all associated equipment - Field execution...

A leading engineering consultancy in pharmaceuticals is seeking a CQ Manager Utilities in Singapore. The role involves overseeing commissioning and qualification of critical utility systems, including WFI/PW, HVAC, and boiler systems, to ensure compliance with operational and regulatory standards. The ideal candidate will have over 10 years of experience in...

Responsibilities Plan and execute temperature mapping studies for cold rooms, warehouses, freezers, incubators, and stability chambers. Perform Commissioning, Qualification, and Validation (CQV) for equipment and facilities. Prepare and review validation protocols (IQ/OQ/PQ), reports, and related GMP documentation. Ensure mapping equipment is properly...

**Location**:Beijing, China **Contract**:Annual, extendable (2-3 year project) We are hiring a **CQV Manager**to lead commissioning, qualification, and validation (CQV) activities for a multinational GMP facility in Beijing. This is a high-impact role in a major pharmaceutical capital project. **What You’ll Do** - Lead CQV strategy, execution, and...

**Responsibilities**: - Develop and execute Commissioning, Qualification, and Validation (CQV) protocols (IQ/OQ/PQ) for **pharmaceutical manufacturing **facilities, equipment, and systems. - Collaborate with project teams to ensure compliance with regulatory standards (e.g., FDA, EMA, GMP). - Perform risk assessments, gap analysis, and prepare validation...

: We are hiring for a number of CQV roles across the Singapore area. We have both short and long term contracts and all are with biotech client project (site based). We are looking for Intermediate to Senior Engineers who will bring their expertise with them and drive our projects to completion. All roles are with Biotech clients. : - Field execution of...

**About the Role**: We invite highly motivated individuals to join our team in providing support to our clients’ biomanufacturing facilities. In this role, you will be tasked with performing pre-commissioning checks and detailed testing, troubleshooting process/equipment issues, preparing comprehensive reports, collaborating with cross-functional teams,...

**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...