Job Description
Position: Pharmaceutical Manufacturing Quality Engineer
Company: GlaxoSmithKline Tanzania
Location: Arusha, Tanzania
Experience: 5+ years in pharmaceutical quality engineering
Education: Bachelor’s degree in Chemical Engineering, Pharmacy, or related field
Employment Type: Full-time
Industry: Pharmaceutical Manufacturing
Department: Quality Assurance
Salary: SSP 2,500,000 – 4,000,000 per month
Vacancies:1
Company Overview
GlaxoSmithKline Tanzania (GSK Tanzania) is a leading global healthcare company dedicated to improving the quality of life through innovative medicines, vaccines, and consumer health products. With a strong presence across East Africa, GSK Tanzania operates state‑of‑the‑art manufacturing facilities in Arusha, adhering to the highest international standards of Good Manufacturing Practice (GMP). The company invests heavily in research, development, and sustainable manufacturing, creating a dynamic environment for professionals who are passionate about health, science, and quality. As part of GSK’s global network, employees in Tanzania benefit from continuous learning, cross‑border collaboration, and a culture that values integrity, transparency, and patient‑centricity. This role offers a unique opportunity to contribute to life‑saving products while advancing your career in a reputable multinational organization.
Job Overview
The Pharmaceutical Manufacturing Quality Engineer will be responsible for ensuring that all manufacturing processes, equipment, and facilities meet stringent quality standards and regulatory requirements. Reporting to the Quality Assurance Manager, you will lead risk‑based assessments, drive continuous improvement initiatives, and collaborate closely with production, validation, and regulatory teams. This position plays a critical role in safeguarding product integrity, supporting GSK’s commitment to delivering safe and effective medicines to patients across Tanzania and the broader region. The role also supports GSK’s strategic objectives of expanding its product portfolio and enhancing operational excellence, making it a pivotal part of the company’s growth trajectory.
For more information, visit our main website https://tanzaniajobsearch.com.
Key Responsibilities
- Develop, implement, and maintain quality engineering procedures aligned with GMP, WHO, and local regulatory guidelines.
- Conduct risk assessments, failure mode and effects analysis (FMEA), and root‑cause investigations for manufacturing deviations.
- Lead validation activities for equipment, processes, and cleaning procedures, ensuring documentation is complete and audit‑ready.
- Collaborate with production teams to optimize process parameters, reduce variability, and improve yield without compromising quality.
- Monitor and analyze key quality metrics, generate trend reports, and recommend corrective and preventive actions (CAPA).
- Support internal and external audits, including FDA, WHO, and Tanzania Food and Drugs Authority (TFDA) inspections.
- Provide technical guidance and training to manufacturing staff on quality standards and best practices.
- Participate in cross‑functional project teams for new product introductions and technology transfers.
Required Skills
- Strong knowledge of GMP, ISO 9001, and pharmaceutical quality systems.
- Proficiency in statistical analysis tools (Minitab, JMP) and quality improvement methodologies (Six Sigma, Lean).
- Excellent problem‑solving abilities with a data‑driven approach.
- Effective communication skills for interfacing with multidisciplinary teams and regulatory bodies.
- Ability to manage multiple projects simultaneously while meeting strict deadlines.
- Familiarity with validation protocols, equipment qualification, and process analytical technology (PAT).
Education
A Bachelor’s degree in Chemical Engineering, Pharmacy, Pharmaceutical Sciences, or a related discipline is required. A Master’s degree or professional certifications such as CQE, Six Sigma Green Belt, or PMP are highly desirable and will be considered an advantage during the selection process.
Experience
Applicants must have a minimum of five years of hands‑on experience in quality engineering within a pharmaceutical manufacturing environment. Experience with GMP compliance, equipment qualification, and leading CAPA investigations is essential. Prior exposure to multinational pharmaceutical companies or contract manufacturing organizations (CMOs) will be viewed favorably.
Salary
The competitive salary range for this position is SSP 2,500,000 to SSP 4,000,000 per month, commensurate with experience and qualifications. In addition to the base salary, GSK Tanzania offers performance‑based bonuses, health insurance, pension contributions, and a comprehensive benefits package.
Benefits
- Comprehensive medical, dental, and vision coverage for employee and dependents.
- Retirement savings plan with employer matching contributions.
- Generous paid time off, including annual leave, sick leave, and public holidays.
- Employee assistance program and wellness initiatives.
- Transportation allowance or company‑provided shuttle service.
- Access to GSK’s global learning platforms and career development resources.
Training
- On‑boarding program covering GSK’s quality culture, GMP fundamentals, and safety protocols.
- Continuous professional development through workshops, webinars, and certifications.
- Mentorship opportunities with senior quality leaders across GSK’s global network.
- Leadership development tracks for high‑potential employees.
Working Environment
GSK Tanzania offers a modern, collaborative workplace equipped with cutting‑edge manufacturing technology and robust quality systems. The Arusha facility emphasizes safety, sustainability, and employee well‑being, fostering an inclusive culture where diverse perspectives are valued. Employees enjoy a supportive atmosphere that encourages innovation, knowledge sharing, and career progression.
Application Process
Interested candidates should submit their updated CV and a cover letter outlining their relevant experience through the online portal on our careers page. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for a virtual interview followed by an on‑site assessment. For additional regional opportunities, explore https://www.southsudanjobsearch.com/.
Equal Opportunity Statement
GlaxoSmithKline Tanzania is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or veteran status.