QC Lab Validation

We are looking for a QC Engineer to support **validation of analytical laboratory instruments and computerized systems**in a GMP-regulated environment. The role focuses on ensuring compliance with 21 CFR Part 11, Annex 11, ALCOA+ principles, and data integrity requirements. **Key Responsibilities**: - Plan, execute, and document qualification/validation of...

Full Job DescriptionWe are seeking an experienced Senior QC Lab Supervisor to lead and oversee laboratory operations for a leading multinational chemical manufacturer based in Jurong Island.You will be responsible for ensuring that all analytical and quality control processes meet company and international standards. The ideal candidate is a hands-on leader...

ES 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...

More than 380! That’s the number of associates in our Singapore Large Molecules division to support the making of medicines for our patients worldwide. - The job is responsible to provides ancillary support services in the QC Laboratory for the routine operations including documentation archiving, dispatching of samples to support all pre and validation...

Overview QC Associate - System Support (Equipment Qualification/ Validation/Pharma)Location : Gul Circle Salary Up to $4,500 depending on experience Completion Bonus 1 Month Our client delivers vital healthcare solutions worldwide, powered by the precision and dedication of its Manufacturing & Supply teams. With your talent, they can expand their...

**Responsibilities**: - Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory equipment (lab bench and CSV system) - Responsible for overseeing execution of but not limited to IQ, OQ, PQ and ERES Test Scripts of QC laboratory equipment (lab...

PES 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...

The Senior Validation Engineer is responsible for the qualification or requalification of laboratory equipment within the targeted schedule. **Responsibilities**: - Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory equipment (lab bench and...

No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services. We strongly uphold our core...

Conduct biochemical analyses under supervision, including cell counts, flow cytometry, ELISA, and PCR analysis, plus basic compendial testing (pH, conductivity, appearance) in line with USP, JP, and EP standards. Assist with documentation and review of results to ensure alignment with current Good Manufacturing Practices (cGMP). Provide general lab support:...