Quality Assurance Engineer Job Vacancy in Thika, Kenya – Healthcare

Job Description

Position:Quality Assurance Engineer

Company:GlaxoSmithKline Kenya

Location:Thika, Kenya

Experience:3-5 years

Education:Bachelor’s degree in Pharmaceutical Sciences, Chemistry, or related field

Employment Type:Full-time

Industry:Healthcare

Department:Quality Assurance

Salary:SSP 150,000 – 250,000 per month

Vacancies:1

Company Overview

GlaxoSmithKline Kenya (GSK Kenya) is a leading global healthcare company dedicated to improving the health and well-being of people worldwide. With a strong presence in Kenya for over three decades, GSK Kenya operates state‑of‑the‑art manufacturing facilities, research laboratories, and a robust distribution network that reaches every corner of the country. The company’s mission is to develop innovative medicines, vaccines, and consumer health products that address the most pressing health challenges in Kenya and across Africa. As a responsible corporate citizen, GSK Kenya invests heavily in community health programs, education initiatives, and sustainable practices, making it a preferred employer for professionals seeking meaningful impact and career growth.

Job Overview

The Quality Assurance Engineer will play a pivotal role in ensuring that all pharmaceutical products manufactured at the Thika facility meet the highest standards of safety, efficacy, and regulatory compliance. Reporting to the QA Manager, the engineer will lead quality investigations, implement robust quality systems, and collaborate closely with production, R&D, and regulatory teams. This position offers a unique opportunity to work within a globally recognized organization, contribute to life‑saving products, and develop expertise in international quality standards such as GMP, ISO 9001, and ICH guidelines. For more information about GSK Kenya’s career opportunities, visit our main website at https://kenyajobsearch.com.

Key Responsibilities

• Develop, maintain, and continuously improve the Quality Management System (QMS) in alignment with GMP and ISO standards.
• Conduct risk assessments, root‑cause analyses, and corrective‑preventive actions (CAPA) for any deviations or non‑conformances.
• Lead internal and external audits, ensuring readiness for regulatory inspections by the Pharmacy and Poisons Board.
• Collaborate with production teams to validate manufacturing processes, equipment qualification, and cleaning procedures.
• Review and approve batch records, specifications, and validation protocols to guarantee product integrity.
• Provide training and mentorship to junior QA staff on quality principles, documentation practices, and regulatory requirements.
• Monitor key quality metrics and generate comprehensive reports for senior management.
• Support new product introductions by ensuring all quality documentation is complete and compliant.

Required Skills

• In‑depth knowledge of Good Manufacturing Practices (GMP) and International Council for Harmonisation (ICH) guidelines.
• Strong analytical and problem‑solving abilities with a data‑driven mindset.
• Excellent written and verbal communication skills for clear documentation and stakeholder interaction.
• Proficiency in quality management software and Microsoft Office Suite.
• Ability to work independently and as part of cross‑functional teams in a fast‑paced environment.
• Attention to detail and a commitment to maintaining the highest standards of product quality.

Education

A Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related discipline is required. Professional certifications such as Certified Quality Engineer (CQE) or Certified Pharmaceutical GMP Professional are advantageous.

Experience

Applicants should have a minimum of three to five years of hands‑on experience in quality assurance within a pharmaceutical manufacturing setting. Experience with regulatory inspections and audit preparation is highly valued.

Salary

The compensation package ranges from SSP 150,000 to SSP 250,000 per month, commensurate with experience and qualifications. The package includes performance‑based bonuses and cost‑of‑living adjustments.

Benefits

• Comprehensive health insurance covering employee and dependents.
• Retirement savings plan with employer contributions.
• Paid annual leave, sick leave, and maternity/paternity leave.
• Employee assistance program and wellness initiatives.
• Transportation allowance and meal vouchers.

Training

• Continuous professional development through GSK’s global learning platform.
• Access to industry‑leading workshops on regulatory affairs, advanced analytics, and quality risk management.
• Mentorship programs pairing new hires with senior QA leaders.
• Opportunities to attend international conferences and seminars.

Working Environment

GSK Kenya offers a collaborative, inclusive, and safety‑focused workplace. The Thika facility is equipped with modern laboratories, controlled‑environment manufacturing suites, and state‑of‑the‑art analytical instruments. Employees benefit from a culture that encourages innovation, respects diversity, and promotes work‑life balance.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining their relevant experience through the online portal. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for a virtual interview. For additional career resources, explore the regional portal at https://tanzaniajobsearch.com/job-vacancy-tanzania/.

Equal Opportunity Statement

GlaxoSmithKline Kenya 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. All qualified applicants will receive consideration for employment without regard to any protected characteristic.