Quality Assurance Manager Job Vacancy in Gunjur, Gambia – Pharmaceutical Manufacturing
Job Description
Position:Quality Assurance Manager
Company:GlaxoSmithKline Gambia
Location:Gunjur, Gambia
Experience:5+ years in pharmaceutical quality assurance
Education:Bachelor’s degree in Pharmacy, Chemistry, or related field
Employment Type:Full-time
Industry:Pharmaceutical Manufacturing
Department:Quality Assurance
Salary:SSP 120,000 – 180,000 per month
Vacancies:1
Company Overview
GlaxoSmithKline (GSK) is a global healthcare leader dedicated to improving the quality of life through innovative medicines, vaccines, and consumer healthcare products. With a strong commitment to the African continent, GSK Gambia operates a state‑of‑the‑art manufacturing facility that adheres to the highest international standards. The company fosters a culture of scientific excellence, ethical conduct, and sustainable practices, offering employees a dynamic environment where career growth aligns with societal impact. As part of GSK’s worldwide network, the Gunjur site plays a pivotal role in delivering high‑quality pharmaceutical products to regional markets, supporting the broader mission of health advancement across West Africa.
Job Overview
The Quality Assurance Manager will lead the QA department to ensure that all products manufactured at the Gunjur facility meet stringent regulatory, safety, and quality standards. This role involves overseeing quality systems, managing audits, and driving continuous improvement initiatives. The successful candidate will collaborate closely with Production, R&D, and Regulatory Affairs to maintain compliance with GMP, WHO, and local health authority requirements. This position offers a unique opportunity to influence product integrity, safeguard public health, and contribute to GSK’s reputation for excellence.
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Key Responsibilities
- Develop, implement, and maintain the Quality Management System (QMS) in alignment with GMP, ISO 9001, and GSK global standards.
- Lead internal and external audits, including regulatory inspections, and ensure timely corrective and preventive actions (CAPA).
- Supervise the release of batches, ensuring all documentation, testing, and release criteria are met before product distribution.
- Coordinate with Production and R&D to resolve quality deviations, investigate root causes, and implement effective solutions.
- Manage the validation and qualification of equipment, processes, and analytical methods.
- Oversee training programs for QA staff and cross‑functional teams on quality principles and regulatory requirements.
- Prepare and present quality performance metrics and reports to senior management.
- Maintain liaison with national regulatory bodies, ensuring all submissions and communications are accurate and timely.
Required Skills
- In‑depth knowledge of GMP, WHO, and local pharmaceutical regulations.
- Strong leadership and team‑management capabilities.
- Excellent analytical and problem‑solving skills with a data‑driven mindset.
- Proficiency in quality risk management tools such as FMEA and HACCP.
- Effective communication skills, both written and verbal, for interfacing with internal and external stakeholders.
- Ability to manage multiple projects simultaneously while meeting strict deadlines.
Education
A minimum of a Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related scientific discipline is required. Advanced certifications such as Certified Quality Auditor (CQA) or a Master’s degree are highly desirable.
Experience
At least five years of progressive experience in pharmaceutical quality assurance, with a minimum of two years in a supervisory or managerial role. Prior experience in a GMP‑regulated manufacturing environment is essential.
Salary
The compensation package ranges from SSP 120,000 to SSP 180,000 per month, commensurate with experience and qualifications. The package includes performance‑based incentives and statutory benefits.
Benefits
- Comprehensive health insurance covering employee and dependents.
- Retirement savings plan with employer contributions.
- Paid annual leave and public holidays in accordance with Gambian labor law.
- Professional development allowance for certifications and conferences.
- Employee assistance program and wellness initiatives.
Training
- Onboarding program covering GSK’s global quality standards and local regulatory expectations.
- Continuous training on latest GMP updates, risk management, and quality tools.
- Leadership development workshops to enhance managerial competencies.
Working Environment
The role is based at GSK’s modern manufacturing campus in Gunjur, featuring advanced laboratory facilities, controlled production zones, and collaborative workspaces. Employees benefit from a safe, inclusive, and environmentally conscious workplace that encourages innovation and teamwork.
Application Process
Interested candidates should submit their updated CV and a cover letter outlining relevant experience through the online portal on the GSK Careers page. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for interviews.
Equal Opportunity Statement
GlaxoSmithKline Gambia is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, irrespective of gender, race, religion, disability, or any other protected characteristic.
