cqv

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...

CQV, Validation & Quality Consultant (Hybride Profile) | Singapore We are seeking a highly versatile CQV, Validation & Quality Consultant (Hybrid Profile) to join our team in Singapore. As a key member, you will deliver end-to-end support for commissioning, qualification, validation, and quality assurance activities across pharma, biotech, and medical device...

Job Description: Contribute to Life Science projects for Antaes Asia clients Act as a core reviewer for CQV documentation and processes, ensuring all qualification activities are thoroughly evaluated and approved. Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and...

The CQV Manager is a senior leadership role responsible for directing commissioning, qualification, and validation (CQV) activities across capital projects, facility expansions, equipment installations, and process improvement initiatives in a GMP-regulated manufacturing environment. The role leads CQV strategy, planning, and execution so that facilities,...

Contribute to Life Science projects for Antaes Asia clients Act as a core reviewer for CQV documentation and processes, ensuring all qualification activities are thoroughly evaluated and approved. Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices. Support...

The CQV Manager is a senior leadership role responsible for directing commissioning, qualification, and validation (CQV) activities across capital projects, facility expansions, equipment installations, and process improvement initiatives in a GMP-regulated manufacturing environment. The role leads CQV strategy, planning, and execution so that facilities,...

CQV, Validation & Quality Consultant (Hybride Profile) | SingaporeWe are seeking a highly versatile CQV, Validation & Quality Consultant (Hybrid Profile) to join our team in Singapore. As a key member, you will deliver end-to-end support for commissioning, qualification, validation, and quality assurance activities across pharma, biotech, and medical device...

CQV / COMMISSIONING ENGINEERProcess Equipment & SkidsProject / Client Site: GSK Plant, Tuas, SingaporeIndustry: Pharmaceutical / Biopharmaceutical ManufacturingFunction: Commissioning, Qualification & Validation (CQV)Employment Type: Project / Contract AssignmentROLE PURPOSEWe are seeking experienced CQV / Commissioning Engineers to support the commissioning...

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...

CQV / COMMISSIONING ENGINEER Process Equipment & Skids Project / Client Site: GSK Plant, Tuas, SingaporeIndustry: Pharmaceutical / Biopharmaceutical ManufacturingFunction: Commissioning, Qualification & Validation (CQV)Employment Type: Project / Contract Assignment ROLE PURPOSE We are seeking experienced CQV / Commissioning Engineers to support the...

About No Deviation At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful...

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...

CQV Manager - Pharmaceutical Manufacturing Full-time Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries. Working with our clients across real estate, infrastructure, energy and natural resources, we transform together delivering outcomes that improve people’s lives. Working in partnership...

CQV Manager - Pharmaceutical Manufacturing Full-time Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries. Working with our clients across real estate, infrastructure, energy and natural resources, we transform together delivering outcomes that improve people’s lives. Working in partnership makes...

WuXi Biologics is a premier provider of biologics services (from discovery to commercialization) with global customers in the biopharmaceutical and healthcare industries. We´re one of the world's top three contract development and manufacturing companies for biopharmaceuticals, we provide our clients with a world-leading open access technology platform. We...

Esco Aster Pte Ltd, part of Esco Lifesciences Group in Singapore, invites a proactive Project Coordinator to join our CQV-focused team. You will plan, coordinate and monitor validation activities across CQV lifecycle in a fast-paced regulated environment. You will partner with Engineering, Facilities, Manufacturing and Quality to ensure on-time delivery,...

Department Description GENG is responsible for capital and expansion construction projects per the Company's business strategic plan, and carry out all-round and whole-process project construction management, including due diligence report, design, civil, MEP and CQV, until delivering the biopharmaceutical R & D and GMP facilities to meet different needs;...

Esco Aster Pte Ltd is seeking a dedicated MSAT CQV professional to lead commissioning, qualification and validation for biopharma equipment, utilities and processes in a GxP setting. You will prepare validation protocols, write reports and coordinate with multiple teams to ensure compliance. The role requires a degree in engineering or science, strong CQV...

NO DEVIATION PTE. LTD. in Singapore seeks a CQV, Validation & Quality Consultant with a hybrid profile to support end-to-end commissioning, qualification, validation and quality assurance across pharma, biotech and medical device projects. You will lead CQV activities, develop validation protocols, prepare QA documents, support regulatory compliance and...

Process Engineering Specialists is seeking experienced Validation Engineers to join our Life Sciences team in Singapore on permanent roles. Strong CQV experience across filling lines, benchtop equipment, utilities, and HVAC/clean air devices is preferred. PES operates globally and values compliant, high-quality validation delivery. You will review and...