GSK
Pharmaceutical
QAManager(PharmaceuticalPracticeCertificaterequired)-18-monthcontract
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“QA Manager (Pharmaceutical Practice Certificate required) - 18-month contract at GSK. Skills: Quality Assurance, Pharmaceutical Oversight, Quality Management System (QMS), Compliance, Risk and Impact Assessments, Batch Release, Stock Disposition, Root Cause Analysis, Risk Assessment, Continuous Improvement. Lead quality assurance and pharmaceutical oversight for Vietnam operations. Partnering with manufacturing, supply, regulatory and external providers to deploy and maintain a robust Quality Ma”
What You'll Achieve.
Deploy and maintain a robust Quality Management System (QMS); Drive compliance; Meet local regulations and GSK QMS requirements; Meet GSK standards, GDP, GSP and local regulatory requirements; Ensuring product quality and regulatory compliance
Industry & Context.
Resolve quality issues with clear practical actions; Root cause analysis; Risk assessment
On-site role requiring regular presence at the local operating site, 18-month contract
What They're Looking For.
Must Have
Bachelor’s degree in Pharmacy or Pharmaceutical Sciences, Pharmaceutical Practice Certificate for vaccines and general medicine (mandatory), Minimum 5 years’ QA experience in pharmaceutical, vaccines or healthcare industry, Practical knowledge of GDP, GSP and GMP aspects relevant to secondary packaging, warehousing and distribution, Demonstrable experience managing deviations, investigations, CAPA and change control, Experience reviewing and approving batch release documentation and performing stock disposition, Fluent in Vietnamese and good working knowledge of English for cross‑functional communication
Nice to Have
Master’s degree or professional accreditation in pharmacy or quality management, Experience in multinational companies and working with third‑party manufacturers or distributors, Familiarity with electronic QMS (eQMS) or SAP, Experience leading audits, regulatory inspections, or preparing regulatory responses, root cause analysis, risk assessment and continuous improvement skills, Proven ability to coach, influence and build effective cross‑functional relationships
What You'll Do.
Lead quality assurance and pharmaceutical oversight for Vietnam operations
Partnering with manufacturing
regulatory and external providers to deploy and maintain a robust Quality Management System (QMS)
Coach cross-functional teams
Resolve quality issues with clear practical actions
Establish and implement processes
systems and GxP documentation
Maintain and continuously improve the local QMS
approve and close quality records including change controls
and validation documentation
Perform risk and impact assessments for operational changes and manage change control decisions
Lead self-inspections and audits of local operations and third‑party service support regulatory inspection readiness
Oversee batch release
stock disposition and final release activities
Coach cross‑functional teams on good documentation practices
incident response and continuous improvement
How You'll Work.
Team & Collaboration
Partnering with manufacturing, supply, regulatory and external providers; Coach cross-functional teams; Build effective cross-functional relationships
Communication Scope
Fluent in Vietnamese; Good working knowledge of English for cross‑functional communication
Process & Methodology
Change Control, CAPA
Full Job Description
## Position summary You will lead quality assurance and pharmaceutical oversight for our Vietnam operations, partnering with manufacturing, supply, regulatory and external providers to deploy and maintain a robust Quality Management System (QMS). You will drive compliance, coach cross-functional teams, resolve quality issues with clear practical actions, and contribute to GSK’s mission of uniting science, technology and talent to get ahead of disease together. This is an on-site role requiring regular presence at the local operating site. **Location:** Ho Chi Minh city. ## Key responsibilities * Establish and implement processes, SOPs, systems and GxP documentation to meet local regulations and GSK QMS requirements. * Maintain and continuously improve the local QMS to meet GSK standards, GDP, GSP and local regulatory requirements. * Review, approve and close quality records including change controls, deviations, investigations, CAPA, and validation documentation for warehouse, equipment and systems. * Perform risk and impact assessments for operational changes and manage change control decisions. * Lead self-inspections and audits of local operations and third‑party service providers; support regulatory inspection readiness. * Oversee batch release, stock disposition and final release activities as required, ensuring product quality and regulatory compliance. * Coach cross‑functional teams on good documentation practices, incident response and continuous improvement. ## Basic qualifications (required) * Bachelor’s degree in Pharmacy or Pharmaceutical Sciences. * Pharmaceutical Practice Certificate for vaccines and general medicine (mandatory). * Minimum 5 years’ QA experience in pharmaceutical, vaccines or healthcare industry. * Practical knowledge of GDP, GSP and GMP aspects relevant to secondary packaging, warehousing and distribution. * Demonstrable experience managing deviations, investigations, CAPA and change control. * Experience reviewing and approving batch
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