cqv manager

The CQV Manager oversees the full validation lifecycle for equipment, facilities, and utilities—from initial requirements and product development through to commercial manufacturing. This role is pivotal in ensuring that all systems are compliant, operational, and maintained to the highest regulatory standards. Key Responsibilities 1. Site SME &...

The CQV Manager oversees the full validation lifecycle for equipment, facilities, and utilities—from initial requirements and product development through to commercial manufacturing. This role is pivotal in ensuring that all systems are compliant, operational, and maintained to the highest regulatory standards. Key Responsibilities 1. Site SME &...

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,...

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,...

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...

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,...

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...

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...

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...

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,...

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...

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: 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...

CQV Engineer – HVAC – Singapore – 24-Month Contract – Life Sciences How would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you! How would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then...

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. ...

Contribute to Life Science projects for Antaes Asia clientsDevelop 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,...

CQV EngineerProcess Equipment | Kaye Validator | Thermal MappingRole OverviewThe CQV Engineer will plan, execute, and document commissioning and qualification activities for pharmaceutical process equipment, temperature-controlled units, and storage areas within a GMP-regulated environment.The role combines hands-on equipment CQV with Kaye-based thermal...

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...

Roles & Responsibilities 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...