cqv

Role Overview The C&Q Lead will provide validation oversight and hands-on support for a 5kL manufacturing project within a GMP-regulated pharmaceutical environment. The role will lead and coordinate commissioning and qualification activities, support cleaning validation where required, and provide validation assistance for other ad hoc site projects. ...

Job Description You'll have the opportunity to work within our Life Sciences team, supporting commissioning, qualification, and validation activities in a pharmaceutical environment. This role is ideal for junior professionals interested in developing their careers in CQV, equipment qualification, and computerized system validation. About The Job ...

Job Description: Contribute to Life Science projects for Antaes Asia clients Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices. Support end-to-end CQV lifecycle for process, utility, and support systems - e.g. bioreactors, chromatography skids,...

We are Coalesce Management Consulting! A community of people with strong Passion for Excellence We deliver bespoke project solutions within Life Science and Technology sectors by Consultative through our community of High Calibre Industry specialists. Our approach is Simple but meaningful – We Grow by Helping Others Grow, We pride ourselves on providing...

About the Role Join our team as a CQV (Commissioning, Qualification & Validation) Engineer , supporting the start-up and validation of state-of-the-art pharmaceutical/biotech manufacturing facilities. You will work closely with project, engineering, and quality teams to ensure all systems meet GMP compliance and are ready for commercial production. Job...

Job Description: Contribute to Life Science projects for Antaes Asia clients Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices. Support end-to-end CQV lifecycle for process, utility, and support systems - e.g. bioreactors, chromatography skids,...

Contribute to Life Science projects for Antaes Asia clients Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices. Support end-to-end CQV lifecycle for process, utility, and support systems — e.g. bioreactors, chromatography skids, filtration units, CIP/SIP,...

Overview AMTSOL is supporting a pharmaceutical manufacturing project in Singapore and is seeking an HVAC CQV Engineer to execute commissioning, qualification, and validation of HVAC systems and Grade C/D cleanrooms in line with EU GMP Annex 1, ISO 14644, and site quality requirements.Key Responsibilities Develop, review, and execute HVAC and cleanroom...

Position Overview The CQV Engineer is responsible for the commissioning, qualification, validation, and lifecycle management of GMP equipment, utilities, and controlled temperature storage systems. The role involves planning and executing temperature mapping studies, developing User Requirement Specifications (URS), generating qualification protocols and...

ALL JOBS LISTED ARE BASED IN SINGAPORE ONLY.FOR SINGAPOREAN ONLY. Job description:• Lead Commissioning, Qualification & Validation (CQV) activities• Lead a team and execute all field work such as Commissioning, Installation & Operational Qualification (IQ/OQ), Validation for downstream process equipment, CIP & Clean utilities to complete assigned...

Responsibilities Execute full-lifecycle qualification (DQ, IQ,OQ, PQ) for a wide range of analytical laboratory instruments, including but not limited to: HPLC/UPLC, GC, Mass Spectrometers, UV-Vis Spectrophotometers, FTIR, Particle Size Analyzers, Dissolution Testers, and Osmometers. Draft and execute validation protocols, risk assessments (FMEA), user...

You’ll have the opportunity to work within our Life Sciences team, supporting commissioning, qualification, and validation activities in a pharmaceutical environment. This role is ideal for junior professionals interested in developing their careers in CQV, equipment qualification, and computerized system validation. ABOUT THE JOB Support commissioning,...

Role Overview The C&Q Lead will provide validation oversight and hands‑on support for a 5kL manufacturing project within a GMP-regulated pharmaceutical environment. The role will lead and coordinate commissioning and qualification activities, support cleaning validation where required, and provide validation assistance for other ad hoc site projects. This...

About the RoleJoin our team as a CQV (Commissioning, Qualification & Validation) Engineer, supporting the start-up and validation of state-of-the-art pharmaceutical/biotech manufacturing facilities. You will work closely with project, engineering, and quality teams to ensure all systems meet GMP compliance and are ready for commercial production.Job...

ALL JOBS LISTED ARE BASED IN SINGAPORE ONLY. FOR SINGAPOREAN ONLY. Job description: ALL JOBS LISTED ARE BASED IN SINGAPORE ONLY. FOR SINGAPOREAN ONLY. Job description: ALL JOBS LISTED ARE BASED IN SINGAPORE ONLY. FOR SINGAPOREAN ONLY. Job description: Lead Commissioning, Qualification & Validation (CQV) activities Lead a team and execute all field work...

Role Overview The C&Q Lead will provide validation oversight and hands‑on support for a 5kL manufacturing project within a GMP‑regulated pharmaceutical environment. The role will lead and coordinate commissioning and qualification activities, support cleaning validation where required, and provide validation assistance for other ad hoc site projects....

CQV Engineer – HVAC – Singapore – 24-Month Contract – Life Sciences How would you like the opportunity to support one of the largest biopharmaceutical projects in the country If yes, then this is the assignment for you! Our client is currently seeking the skills of a CQV Engineer to support their team. Our client develops and delivers life...

Location: SingaporeEmployment Type: ContractExperience Level: Junior to SeniorMinimum Experience: 2 years Role Overview We are looking for Validation Engineers with Commissioning & Qualification (CQV) experience to support a major pharmaceutical manufacturing project in Singapore. The successful candidates will support and execute commissioning,...

Job Description: Contribute to Life Science projects for Antaes Asia clients Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices. Support end-to-end CQV lifecycle for process, utility, and support systems - e.g. bioreactors, chromatography skids,...

Responsibilities Execute full-lifecycle qualification (DQ, IQ,OQ, PQ) for a wide range of analytical laboratory instruments, including but not limited to: HPLC/UPLC, GC, Mass Spectrometers, UV-Vis Spectrophotometers, FTIR, Particle Size Analyzers, Dissolution Testers, and Osmometers. Draft and execute validation protocols, risk assessments (FMEA), user...