Job Description
Position: Pharmaceutical Manufacturing Quality Engineer
Company: GlaxoSmithKline Botswana
Location: Mochudi, Botswana
Experience: 5+ years in pharmaceutical manufacturing quality engineering
Education: Bachelor’s degree in Chemical Engineering, Pharmaceutical Sciences or related field
Employment Type: Full-time
Industry: Pharmaceutical Manufacturing
Department: Quality Assurance
Salary: SSP 120,000 – 180,000 per annum
Vacancies:1
Company Overview
GlaxoSmithKline Botswana is a leading global healthcare company dedicated to improving the health and well‑being of people worldwide. With a strong presence in Botswana, GSK operates state‑of‑the‑art manufacturing facilities that produce high‑quality medicines, vaccines, and consumer health products. The company’s commitment to innovation, compliance, and sustainable practices makes it an employer of choice for professionals seeking a dynamic and purpose‑driven career.
GSK Botswana invests heavily in research and development, leveraging cutting‑edge technologies to ensure product safety, efficacy, and regulatory excellence. The organization fosters a collaborative culture where cross‑functional teams work together to solve complex challenges, drive continuous improvement, and deliver life‑saving therapies to patients across the region.
As part of its corporate social responsibility, GSK actively supports community health initiatives, education programs, and environmental stewardship projects throughout Botswana. Employees are encouraged to participate in volunteer activities, professional development, and mentorship programs that enhance both personal growth and societal impact.
Job Overview
The Pharmaceutical Manufacturing Quality Engineer will play a pivotal role in ensuring that all manufacturing processes meet the highest standards of quality, safety, and regulatory compliance. Reporting to the Senior Quality Manager, the engineer will lead quality risk assessments, drive process improvements, and collaborate closely with production, validation, and regulatory teams to maintain GSK’s reputation for excellence.
This position offers a unique opportunity to work within a world‑class facility, applying advanced engineering principles to real‑world pharmaceutical production challenges. The successful candidate will be instrumental in shaping the quality culture, implementing robust control strategies, and supporting the launch of new products that address critical health needs.
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Key Responsibilities
- Develop, implement, and maintain quality engineering procedures aligned with GMP, ISO 9001, and local regulatory requirements.
- Conduct risk assessments (FMEA, HACCP) and root‑cause investigations for deviations, non‑conformances, and CAPA initiatives.
- Collaborate with process engineers to design and validate manufacturing processes, ensuring robustness and reproducibility.
- Lead continuous improvement projects using Lean Six Sigma methodologies to enhance product quality and operational efficiency.
- Support technology transfer activities, providing quality engineering expertise for new product introductions.
- Prepare and review technical documentation, including batch records, validation protocols, and change control submissions.
- Act as a subject matter expert during internal and external audits, ensuring successful audit outcomes.
- Mentor junior engineers and quality staff, fostering a culture of learning and compliance.
Required Skills
- Strong knowledge of GMP, FDA, EMA, and Botswana Pharmacy Board regulations.
- Proficiency in statistical analysis tools (Minitab, JMP) and data‑driven decision making.
- Excellent problem‑solving abilities with a systematic approach to root‑cause analysis.
- Effective communication skills for cross‑functional collaboration and stakeholder engagement.
- Project management experience, including planning, execution, and monitoring of quality initiatives.
- Familiarity with validation lifecycle (IQ/OQ/PQ) and equipment qualification.
Education
A Bachelor’s degree in Chemical Engineering, Pharmaceutical Sciences, Mechanical Engineering, or a related discipline is required. Advanced certifications such as Certified Quality Engineer (CQE) or Lean Six Sigma Black Belt are highly desirable.
Experience
Minimum of five years’ experience in quality engineering within a pharmaceutical manufacturing environment, with a proven track record of leading successful compliance and improvement projects.
Salary
The competitive salary range for this role is SSP 120,000 – 180,000 per annum, commensurate with experience and qualifications. Additional performance‑based incentives may be offered.
Benefits
- Comprehensive health insurance covering employee and dependents.
- Retirement savings plan with employer contributions.
- Generous paid leave, including annual, sick, and parental leave.
- Professional development budget for certifications, workshops, and conferences.
- Employee assistance program and wellness initiatives.
Training
- On‑boarding program covering GSK’s quality systems, safety protocols, and corporate values.
- Continuous training in GMP, regulatory updates, and advanced quality engineering tools.
- Leadership development pathways for high‑potential engineers.
Working Environment
The role is based in GSK’s modern manufacturing plant in Mochudi, featuring controlled clean‑room environments, advanced analytical laboratories, and collaborative workspaces. Employees benefit from a safety‑first culture, state‑of‑the‑art equipment, and a supportive team atmosphere.
Application Process
Interested candidates should submit their updated CV and a cover letter outlining relevant experience through the online portal. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for interviews.
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Equal Opportunity Statement
GlaxoSmithKline Botswana is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of gender, race, religion, age, disability, or sexual orientation.