
CQV Engineer
4 days ago
Overview Join to apply for the CQV Engineer (Utilities)role at No deviation 3 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. This range is provided by No deviation. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range 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 projects and drive innovation. We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That\'s why we foster a culture of collaboration, inclusion, and continuous development empowering our team members to grow personally and professionally. Position Overview The CQV Engineer (Utilities Qualification) is responsible for the commissioning, qualification, and validation of critical utility systems such as Water for Injection (WFI), Purified Water, Clean Steam, Compressed Dry Air (CDA), HVAC, and other facility support systems. The role ensures that all systems are installed, tested, and qualified in compliance with cGMP, regulatory requirements, and project-specific standards. Key Responsibilities Lead and execute commissioning and qualification activities for utilities (WFI, Purified Water, Clean Steam, CDA, HVAC, and related systems). Develop and execute lifecycle documents including URS, DQ, FAT, SAT, IQ, OQ, PQ protocols and reports. Perform risk assessments, system impact assessments, and component classifications in accordance with ASTM E2500 and USP. Coordinate with vendors, contractors, and internal stakeholders during commissioning and qualification activities. Conduct and document sampling, testing, and verification of utility systems (e.g., TOC, conductivity, microbial testing for water systems). Support troubleshooting, deviation management, and implementation of corrective and preventive actions (CAPAs). Ensure all activities comply with GMP, GDP, safety, and environmental standards. Assist in audits, regulatory inspections, and client reviews by providing documentation and technical expertise. Contribute to continuous improvement initiatives and knowledge sharing across project teams. Required Qualifications Bachelors Degree in Engineering, Life Sciences, or related discipline 10 years experience in CQV for utilities systems in the pharmaceutical / biotech industry. Strong knowledge of GMP guidelines, USP/EP, ISPE Baseline Guides, ASTM E2500, and Annex 15. Hands-on experience with water systems, clean steam, compressed gases, and HVAC qualification. Familiarity with laboratory testing and monitoring equipment (TOC analyzers, conductivity meters, microbial sampling). Strong problem-solving, documentation, and stakeholder communication skills. Ability to work independently and as part of a cross-functional project team. Why join us?Generous Leave Policy including 3 days to care for aging family members, reflecting our commitment to family wellbeing. Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs. Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company. Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated. Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career. How To Apply Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you\'re passionate about making an impact, we want you on our teamPlease submit your resume, outlining your qualifications and experience relevant to the role, here. Seniority level Mid-Senior level Employment type Full-time Job function Engineering and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at No deviation by 2x Get notified about new Utilities Engineer jobs in Singapore, Singapore . #J-18808-Ljbffr
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CQV Engineer
23 hours ago
Singapore MORIMATSU PHARMADULE (SINGAPORE) PTE. LTD. Full time $90,000 - $120,000 per yearAbout 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...
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CQV Engineer
2 weeks ago
Singapore LANYOU TECH PTE. LTD. Full time $90,000 - $120,000 per yearJob DescriptionThe CQV Engineer is responsible for the commissioning, qualification, and validation of CU/Cleanroom/Temperature Controlled Unit/Process systems. The role ensures that all systems are installed, tested, and qualified in compliance with cGMP, regulatory requirements, and project-specific standards.RequirementsBachelors Degree in Engineering,...
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Cqv Engineer
2 days ago
Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time**PharmEng Technology**has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their...
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Junior Project Manager
4 days ago
Singapore PHARMENG TECHNOLOGY PTE. LTD. Full timeCommissioning / Qualification and Verification (CQV) Engineer (Singapore) PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure...
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CQV Engineer
23 hours ago
Singapore Unison Group Full time $90,000 - $120,000 per yearRole OverviewWe are seeking a CQV Engineer with specialized experience in temperature mapping of controlled temperature chambers in GMP/GDP environments. The role requires strong knowledge of GDP principles, ALCOA data integrity standards, and experience authoring protocols and reports in Kneat. Key Responsibilities· Plan and execute temperature mapping...
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CQV Engineer
5 days ago
Singapore Unison Group Full time $60,000 - $180,000 per yearRole OverviewWe are seeking a CQV Engineer with specialized experience in temperature mapping of controlled temperature chambers in GMP/GDP environments. The role requires strong knowledge of GDP principles, ALCOA data integrity standards, and experience authoring protocols and reports in Kneat. Key ResponsibilitiesPlan and execute temperature mapping...
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CQV Engineer
23 hours ago
Singapore Unison Group Full time $90,000 - $120,000 per yearRole OverviewWe are seeking a CQV Engineer with specialized experience in temperature mapping of controlled temperature chambers in GMP/GDP environments. The role requires strong knowledge of GDP principles, ALCOA data integrity standards, and experience authoring protocols and reports in Kneat. Key Responsibilities· Plan and execute temperature mapping...
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Senior CQV Engineer
22 hours ago
Singapore Coalesce Management Consulting Full time $90,000 - $120,000 per yearPosition: Senior CQV EngineerJob DescriptionWe are currently expanding our team and are looking for a Senior CQV Engineer for our project on site with our client.You will be responsible for planning, writing, implementing and reviewing Validation protocols in place within highly regulated environments. Your expertise will lend a hand in tactical...
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Senior CQV Engineer
1 week ago
Singapore NUSANTARA PRIME CONSULTING PTE. LTD. Full time $90,000 - $120,000 per yearResponsibilities:The incumbent will lead commissioning, qualification, and validation (CQV) activities for Lab Equipment.About You:Diploma/Degree in Engineering or Science Disciplines with at least 5 years' experience in lab equipment CSV (computer system validation).Preferably 5 – 10 years experience in analytical instrument CSV.Knowledge towards...
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CQV Engineer
2 weeks ago
Singapore GOOD JOB CREATIONS (SINGAPORE) PTE. LTD. Full timeResponsibilities: Plan, execute, and manage commissioning, qualification, and validation (CQV) activities for pharmaceutical/biotech manufacturing facilities, utilities, and process equipment. Develop and review CQV protocols (IQ/OQ/PQ) and reports in compliance with GMP, GAMP 5, and company procedures. Coordinate with engineering, project, and quality...