Pharmaceutical Quality Assurance Manager Job Vacancy in Thiès, Senegal – Pharmaceuticals
Job Description
Position: Pharmaceutical Quality Assurance Manager
Company: Sanofi
Location: Thiès, Senegal
Experience: Minimum 5 years in pharmaceutical quality assurance, GMP compliance, and regulatory affairs
Education: Bachelor’s degree in Pharmacy, Chemistry, or related field; Master’s degree preferred
Employment Type: Full-time
Industry: Pharmaceuticals
Department: Quality Assurance
Salary: 1,200,000 – 1,800,000 SSP per month
Vacancies:1
Company Overview
Sanofi is a global healthcare leader dedicated to improving lives through innovative medicines, vaccines, and consumer healthcare products. With a strong presence in Senegal, Sanofi operates state‑of‑the‑art manufacturing facilities and a robust distribution network that supports the country’s growing demand for high‑quality pharmaceutical solutions. The company’s commitment to research, development, and sustainable practices makes it an attractive employer for professionals seeking to make a meaningful impact in the health sector. As part of Sanofi’s expansion strategy, the Thiès site plays a pivotal role in regional production, ensuring that essential medicines reach patients across West Africa. Joining Sanofi means becoming part of a diverse, inclusive workforce that values continuous learning, ethical standards, and community engagement. This is an excellent opportunity for candidates who are passionate about quality, compliance, and advancing public health in Senegal.
Sanofi’s presence in Senegal aligns with national goals for healthcare accessibility and economic development. The company collaborates closely with local authorities, academic institutions, and industry partners to foster innovation and capacity building. By investing in talent and technology, Sanofi contributes to the creation of high‑skill jobs and supports the broader ecosystem of pharmaceutical manufacturing in the region. Candidates will benefit from a dynamic environment that encourages professional growth, cross‑functional collaboration, and exposure to international best practices.
Job Overview
The Pharmaceutical Quality Assurance Manager will lead the QA team at Sanofi’s Thiès facility, overseeing all aspects of quality systems, GMP compliance, and regulatory submissions. This role is critical to ensuring that products meet the highest standards of safety, efficacy, and quality before they reach the market. The manager will work closely with production, R&D, and regulatory affairs to implement robust quality strategies, conduct audits, and drive continuous improvement initiatives. The position offers a unique blend of strategic leadership and hands‑on technical expertise, providing a platform to influence the quality culture across the organization. As a senior member of the QA department, the manager will also mentor junior staff, foster a proactive quality mindset, and represent Sanofi in interactions with health authorities and external auditors. This role is essential for maintaining Sanofi’s reputation for excellence and supporting the company’s mission to deliver life‑saving medicines to patients throughout Senegal and the wider West African region.
In addition to core QA responsibilities, the manager will contribute to cross‑functional projects aimed at optimizing manufacturing processes, reducing waste, and enhancing product traceability. The role requires a deep understanding of international regulatory frameworks such as WHO, EMA, and FDA guidelines, as well as local Senegalese health regulations. The successful candidate will be instrumental in shaping the future of Sanofi’s quality operations, ensuring compliance, and driving innovation in quality assurance practices.
https://www.moroccojobsearch.com/
Key Responsibilities
- Lead and manage the Quality Assurance team to ensure compliance with GMP, WHO, EMA, and FDA standards.
- Develop, implement, and maintain quality management systems, SOPs, and documentation.
- Plan and execute internal audits, supplier audits, and readiness assessments for regulatory inspections.
- Oversee deviation investigations, CAPA implementation, and root‑cause analysis.
- Collaborate with Production, R&D, and Regulatory Affairs to support new product introductions and technology transfers.
- Prepare and submit regulatory dossiers, ensuring timely and accurate documentation.
- Drive continuous improvement initiatives using Lean, Six Sigma, or similar methodologies.
- Mentor and train QA staff, fostering a culture of quality and compliance.
- Maintain effective communication with health authorities and external auditors.
- Monitor key quality metrics and generate performance reports for senior management.
Required Skills
- Strong knowledge of GMP, WHO, EMA, and FDA regulations.
- Proven experience in leading QA teams within pharmaceutical manufacturing.
- Excellent analytical, problem‑solving, and decision‑making abilities.
- Effective communication and stakeholder management skills.
- Proficiency in quality management software and data analysis tools.
- Project management experience with a focus on regulatory compliance.
- Ability to work in a multicultural, fast‑paced environment.
Education
A Bachelor’s degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or a related discipline is required. A Master’s degree or professional certifications such as CQE, CQA, or Six Sigma Green Belt are highly desirable and will be considered an advantage during the selection process.
Experience
Applicants must have a minimum of five years of progressive experience in pharmaceutical quality assurance, including at least two years in a supervisory or managerial capacity. Experience with international regulatory submissions and audit preparation is essential.
Salary
The position offers a competitive salary ranging from 1,200,000 to 1,800,000 SSP per month, commensurate with experience and qualifications. Additional performance‑based incentives may be provided.
Benefits
- Comprehensive health insurance covering employee and dependents.
- Retirement savings plan with employer contributions.
- Paid annual leave and public holidays.
- Professional development allowance.
- Employee assistance program and wellness initiatives.
Training
- Onboarding program covering Sanofi’s quality systems and corporate culture.
- Continuous training in GMP, regulatory updates, and advanced QA methodologies.
- Opportunities to attend international conferences and workshops.
- Leadership development courses for managerial growth.
Working Environment
Sanofi’s Thiès facility provides a modern, safe, and collaborative workplace equipped with cutting‑edge technology. The environment encourages teamwork, innovation, and a strong focus on employee well‑being. Employees benefit from a supportive culture that values diversity, inclusion, and work‑life balance.
Application Process
Interested candidates should submit their updated CV and a cover letter outlining their relevant experience through the online portal on Sanofi’s career website. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for a virtual interview followed by an on‑site assessment.
Equal Opportunity Statement
Sanofi is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of gender, age, disability, ethnicity, religion, or sexual orientation. All qualified applicants will receive consideration for employment without discrimination.
