Quality Assurance Engineer Job Vacancy in Enugu, Nigeria – Pharmaceutical Manufacturing
Job Description
Position: Quality Assurance Engineer
Company: Pfizer Nigeria
Location: Enugu, Nigeria
Experience: 3-5 years
Education: B.Sc. in Chemical Engineering or related field
Employment Type: Full-time
Industry: Pharmaceutical Manufacturing
Department: Quality Assurance
Salary: ₦2,500,000 – ₦3,500,000 per annum
Vacancies:1
Company Overview
Pfizer Nigeria is a leading global biopharmaceutical company dedicated to improving health outcomes across the continent. With a strong presence in Nigeria, Pfizer combines cutting‑edge research, robust manufacturing capabilities, and a commitment to local talent development. The company operates state‑of‑the‑art facilities that adhere to international Good Manufacturing Practices (GMP) and contributes significantly to the nation’s healthcare ecosystem. As part of Pfizer’s expansive network, employees in Enugu enjoy access to world‑class resources, continuous learning opportunities, and a collaborative environment that fosters innovation. This role offers a unique chance to be part of a dynamic team that drives quality excellence in pharmaceutical production, supporting Nigeria Jobs and broader Career Opportunities in Nigeria.
Job Overview
The Quality Assurance Engineer will play a pivotal role in ensuring that all pharmaceutical products manufactured at the Enugu site meet stringent regulatory standards and internal quality benchmarks. Reporting to the QA Manager, the engineer will develop, implement, and monitor quality systems, conduct risk assessments, and lead continuous improvement initiatives. This position is essential for maintaining product integrity, safeguarding patient safety, and upholding Pfizer’s reputation for excellence. Candidates will engage with cross‑functional teams, including Production, Validation, and Regulatory Affairs, to drive compliance and operational efficiency.
Key Responsibilities
- Develop, review, and maintain quality assurance procedures, SOPs, and work instructions in line with GMP and local regulatory requirements.
- Conduct internal audits, gap analyses, and corrective‑and‑preventive action (CAPA) investigations to ensure continuous compliance.
- Collaborate with Production and Engineering teams to design and execute validation protocols for equipment, processes, and cleaning procedures.
- Perform risk assessments using tools such as FMEA and HACCP to identify potential quality issues and implement mitigation strategies.
- Lead investigations of product deviations, out‑of‑specification results, and customer complaints, providing thorough root‑cause analysis and effective resolutions.
- Maintain comprehensive documentation and ensure accurate record‑keeping for all quality activities.
- Support regulatory inspections and audits by preparing documentation, facilitating site tours, and addressing auditor queries.
- Drive continuous improvement projects aimed at enhancing product quality, process efficiency, and cost effectiveness.
Required Skills
- Strong knowledge of GMP, ISO 9001, and pharmaceutical quality systems.
- Proficiency in statistical analysis tools and quality software (e.g., Minitab, QMS).
- Excellent problem‑solving abilities with a data‑driven approach.
- Effective communication skills for cross‑functional collaboration and stakeholder engagement.
- Attention to detail and a commitment to maintaining the highest standards of product safety.
- Ability to manage multiple projects simultaneously and meet tight deadlines.
Education
A bachelor’s degree in Chemical Engineering, Pharmaceutical Sciences, Biotechnology, or a related discipline is required. Professional certifications such as Certified Quality Engineer (CQE) or Six Sigma Green Belt are advantageous.
Experience
Applicants must have 3‑5 years of hands‑on experience in quality assurance within a regulated pharmaceutical manufacturing environment. Experience with process validation, audit management, and regulatory submissions is highly valued.
Salary
The annual compensation package ranges from ₦2,500,000 to ₦3,500,000, commensurate with experience and qualifications. The package includes performance‑based bonuses and comprehensive benefits.
Benefits
- Competitive health insurance covering employee and dependents.
- Retirement savings plan with company matching contributions.
- Paid annual leave, sick leave, and public holidays.
- Professional development allowance for certifications and training.
- Employee assistance program and wellness initiatives.
Training
- On‑boarding program covering GMP, company policies, and safety protocols.
- Continuous training in advanced quality tools, regulatory updates, and leadership development.
- Access to Pfizer’s global learning platform for e‑learning courses and webinars.
Working Environment
Pfizer Nigeria offers a modern, safety‑focused workplace equipped with cutting‑edge laboratory and manufacturing facilities. The Enugu site promotes a culture of collaboration, diversity, and inclusion, encouraging employees to share ideas and drive innovation. Flexible working arrangements and a supportive management team ensure a healthy 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 interviews. For more details on the application steps, visit our career page.
https://botswanajobsearch.com/
Equal Opportunity Statement
Pfizer Nigeria is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of gender, race, religion, or sexual orientation. All qualified applicants will receive consideration for employment without discrimination.
