- North Bridge Road Downtown Core Central Region (Singapore) Singapore
Kerja Sepenuh Masa CQV (Commissioning, Qualification - Validation) Engineer, Gaji tinggi SGD 7,500 di JDA WMS PTE. LTD. Central Region (Singapore) - Maukerja
CQV (Commissioning, Qualification - Validation) Engineer
JDA WMS PTE. LTD.
Kongsi
Simpan
Lokasi Kerja
Penerangan Kerja
Tanggungjawab
Position Overview
We are seeking a qualified CQV Engineer to join our project team in driving commissioning, qualification, and validation initiatives for advanced pharmaceutical and biotech manufacturing facilities. Working collaboratively across engineering, project, and quality functions, you will ensure facility systems, clean utilities, and process equipment satisfy strict regulatory standards and operational readiness goals.
Key Responsibilities
CQV Lifecycle Management: Plan, prepare, and execute commissioning, qualification, and validation activities across pharmaceutical utilities, process equipment, and facility systems.
Protocol & Documentation: Author and review IQ/OQ/PQ protocols and execution reports in strict alignment with GMP, GAMP 5, and organizational guidelines.
Testing & Inspection: Support Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), and risk management activities for new or modified equipment.
Regulatory Governance: Ensure full compliance with international regulatory frameworks (FDA, EMA, PIC/S) and local health authority standards.
Cross-Functional Collaboration: Partner with engineering, quality, and construction teams to resolve technical deviations, provide design inputs, and support operational startup.
Requirements
Education: Bachelor’s Degree in Engineering, Life Sciences, or a related discipline.
Experience: 2 to 5 years of hands-on CQV experience within the biopharmaceutical or life sciences sector.
Technical Standards: Solid familiarity with GMP, GAMP 5, ISPE Baseline Guides, and international regulatory expectations.
Utility & Equipment Expertise: Hands-on background with pharmaceutical utilities (WFI, Clean Steam, HVAC), process machinery, or cleanroom environments.
Core Competencies: Strong technical problem-solving capabilities alongside effective cross-team coordination skills.
If interested, please submit your application to ************* with your expected salary and resume.
We regret that only short-listed candidates will be contacted shortly. By submitting your application or resume, you agree to the collection, use, retention, and sharing of your personal information with potential employers for their assessment.
JDA WMS Pte Ltd | EA Personnel: Pham Thi Tuyet Mai
EA License No: 23S1595 | EA Registration No: R25127838
JDA WMS is a global leader in the world of recruitment and matching systems. Leveraging cutting-edge technologies, we bridge the gap between candidates' aspirations and organizations' needs. Our unparalleled expertise lies in delivering bespoke solutions, ensuring impeccable candidate job alignment.
With a strong emphasis on diversity, quality, and innovation, JDA WMS stands at the forefront of transforming recruitment landscapes worldwide, making every match count.
Website: *************
Phone: +************* 6568
If interested, please submit your application to ************* with your expected salary and resume.
We are seeking a qualified CQV Engineer to join our project team in driving commissioning, qualification, and validation initiatives for advanced pharmaceutical and biotech manufacturing facilities. Working collaboratively across engineering, project, and quality functions, you will ensure facility systems, clean utilities, and process equipment satisfy strict regulatory standards and operational readiness goals.
Key Responsibilities
CQV Lifecycle Management: Plan, prepare, and execute commissioning, qualification, and validation activities across pharmaceutical utilities, process equipment, and facility systems.
Protocol & Documentation: Author and review IQ/OQ/PQ protocols and execution reports in strict alignment with GMP, GAMP 5, and organizational guidelines.
Testing & Inspection: Support Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), and risk management activities for new or modified equipment.
Regulatory Governance: Ensure full compliance with international regulatory frameworks (FDA, EMA, PIC/S) and local health authority standards.
Cross-Functional Collaboration: Partner with engineering, quality, and construction teams to resolve technical deviations, provide design inputs, and support operational startup.
Requirements
Education: Bachelor’s Degree in Engineering, Life Sciences, or a related discipline.
Experience: 2 to 5 years of hands-on CQV experience within the biopharmaceutical or life sciences sector.
Technical Standards: Solid familiarity with GMP, GAMP 5, ISPE Baseline Guides, and international regulatory expectations.
Utility & Equipment Expertise: Hands-on background with pharmaceutical utilities (WFI, Clean Steam, HVAC), process machinery, or cleanroom environments.
Core Competencies: Strong technical problem-solving capabilities alongside effective cross-team coordination skills.
If interested, please submit your application to ************* with your expected salary and resume.
We regret that only short-listed candidates will be contacted shortly. By submitting your application or resume, you agree to the collection, use, retention, and sharing of your personal information with potential employers for their assessment.
JDA WMS Pte Ltd | EA Personnel: Pham Thi Tuyet Mai
EA License No: 23S1595 | EA Registration No: R25127838
JDA WMS is a global leader in the world of recruitment and matching systems. Leveraging cutting-edge technologies, we bridge the gap between candidates' aspirations and organizations' needs. Our unparalleled expertise lies in delivering bespoke solutions, ensuring impeccable candidate job alignment.
With a strong emphasis on diversity, quality, and innovation, JDA WMS stands at the forefront of transforming recruitment landscapes worldwide, making every match count.
Website: *************
Phone: +************* 6568
If interested, please submit your application to ************* with your expected salary and resume.
Peringatan Penting
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