- Bukit Merah Central Region (Singapore) Singapore
Full Time Senior QA Specialist (Pharmaceutical) Jobs, Salary up to SGD 8,500 in Kingsforce Management Services Pte. Ltd. Central Region (Singapore) - Maukerja
Senior QA Specialist (Pharmaceutical)
Kingsforce Management Services Pte. Ltd.
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Job Description
Responsibilities
About our client
: Our client is a leading global pharmaceutical company.
About the role
:
Support Singapore Operations facility start-up during commissioning, qualification, and validation of facilities for subsequent clinical and commercial manufacturing.
Support validation business processes across the campus, including process, facility, aseptic, and cleaning validation.
Work cross-functionally with Manufacturing, Engineering, QC, MS&T, and IT teams.
Guide execution and provide QA oversight during commissioning, qualification, and validation of manufacturing equipment, utilities, QC instruments, computerized systems, and facilities.
Support execution of core quality processes, ensuring timely and accurate documentation and data integrity.
Provide direct, on-the-floor QA oversight to ensure activities align with cGMP, approved procedures, and the site pharmaceutical quality system.
Review and approve qualification and validation deliverables, changes within the change management framework, deviation records, reports, and related documentation.
Advise on GxP expectations and actively participate in audits, inspections, and health authority interactions.
Identify, assess, and communicate quality risks, and ensure risks are appropriately managed.
Conduct independent analysis and provide insights on quality metrics and KPIs, translating trends into actions that improve compliance and reliability.
Deliver quality training and coach early-career team members on processes, systems, digital tools, and compliance.
About you:
Bachelor's or Master's degree in a science or technical field such as Biotechnology, Pharmaceutical Sciences, Engineering, Biology, or Chemistry.
Minimum 10 years of validation experience working in a sizeable QA function within pharmaceutical or biopharmaceutical highly regulated manufacturing environments.
Strong understanding of cGMP requirements, regulatory trends, and Pharmaceutical Quality Systems.
Experience providing quality oversight within manufacturing/QC, validation, and related operations.
Excellent oral and written communication, collaboration, and stakeholder management skills, with proactive leadership and a strong quality mindset.
Ability to make sound, risk-based decisions in a fast-paced operational environment.
Strong negotiating and influencing skills, analytical and problem-solving skills, with the ability to manage complex quality issues.
Experience supporting investigations, deviation management, CAPAs, and risk assessments.
Ability to interpret regulatory requirements and apply them within operational settings.
Strong organizational skills with the ability to manage multiple priorities and changing business needs, with a desire to support manufacturing operations.
Experience across several areas, including biological, synthetic active pharmaceutical ingredients, sterile/aseptic, and biopharmaceutical manufacturing environments.
Experience with significant validation programs, including greenfield or brownfield projects.
Experience and knowledge of using digital pharmaceutical systems, data visualization platforms, or analytics solutions to improve quality outcomes.
Experience supporting digital, automation, or AI-enabled transformation initiatives within a GxP environment, with strong knowledge of the testing lifecycle.
Familiarity with process improvement methodologies such as Lean, Six Sigma, or operational excellence frameworks.
Other:
Employment Type: Project-based contract role
Work Schedule: 5 days per week
Location: Tuas, Singapore
Employment Agency Licence No: 94C3545
EA Personnel: Kimberly Wong
EA Personnel Reg. No.: R1984508
A specialized recruitment firm with more than30 years of track records recruiting in the Construction, Oil & Gas, and Pharma industries. We work with Fortune 500 companies and state-owned companies for Singapore & overseas hiring demands.
Kingsforce Management Services Pte. Ltd. | EA Licence: 94C3545
: Our client is a leading global pharmaceutical company.
About the role
:
Support Singapore Operations facility start-up during commissioning, qualification, and validation of facilities for subsequent clinical and commercial manufacturing.
Support validation business processes across the campus, including process, facility, aseptic, and cleaning validation.
Work cross-functionally with Manufacturing, Engineering, QC, MS&T, and IT teams.
Guide execution and provide QA oversight during commissioning, qualification, and validation of manufacturing equipment, utilities, QC instruments, computerized systems, and facilities.
Support execution of core quality processes, ensuring timely and accurate documentation and data integrity.
Provide direct, on-the-floor QA oversight to ensure activities align with cGMP, approved procedures, and the site pharmaceutical quality system.
Review and approve qualification and validation deliverables, changes within the change management framework, deviation records, reports, and related documentation.
Advise on GxP expectations and actively participate in audits, inspections, and health authority interactions.
Identify, assess, and communicate quality risks, and ensure risks are appropriately managed.
Conduct independent analysis and provide insights on quality metrics and KPIs, translating trends into actions that improve compliance and reliability.
Deliver quality training and coach early-career team members on processes, systems, digital tools, and compliance.
About you:
Bachelor's or Master's degree in a science or technical field such as Biotechnology, Pharmaceutical Sciences, Engineering, Biology, or Chemistry.
Minimum 10 years of validation experience working in a sizeable QA function within pharmaceutical or biopharmaceutical highly regulated manufacturing environments.
Strong understanding of cGMP requirements, regulatory trends, and Pharmaceutical Quality Systems.
Experience providing quality oversight within manufacturing/QC, validation, and related operations.
Excellent oral and written communication, collaboration, and stakeholder management skills, with proactive leadership and a strong quality mindset.
Ability to make sound, risk-based decisions in a fast-paced operational environment.
Strong negotiating and influencing skills, analytical and problem-solving skills, with the ability to manage complex quality issues.
Experience supporting investigations, deviation management, CAPAs, and risk assessments.
Ability to interpret regulatory requirements and apply them within operational settings.
Strong organizational skills with the ability to manage multiple priorities and changing business needs, with a desire to support manufacturing operations.
Experience across several areas, including biological, synthetic active pharmaceutical ingredients, sterile/aseptic, and biopharmaceutical manufacturing environments.
Experience with significant validation programs, including greenfield or brownfield projects.
Experience and knowledge of using digital pharmaceutical systems, data visualization platforms, or analytics solutions to improve quality outcomes.
Experience supporting digital, automation, or AI-enabled transformation initiatives within a GxP environment, with strong knowledge of the testing lifecycle.
Familiarity with process improvement methodologies such as Lean, Six Sigma, or operational excellence frameworks.
Other:
Employment Type: Project-based contract role
Work Schedule: 5 days per week
Location: Tuas, Singapore
- Please note that only shortlisted candidates will be contacted.*
Employment Agency Licence No: 94C3545
EA Personnel: Kimberly Wong
EA Personnel Reg. No.: R1984508
A specialized recruitment firm with more than30 years of track records recruiting in the Construction, Oil & Gas, and Pharma industries. We work with Fortune 500 companies and state-owned companies for Singapore & overseas hiring demands.
Kingsforce Management Services Pte. Ltd. | EA Licence: 94C3545
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