Pharmaceutical Quality Assurance Manager Job Vacancy in Louga, Senegal – Healthcare & Life Sciences

Job Description

Position: Pharmaceutical Quality Assurance Manager

Company: Sanofi

Location: Louga, Senegal

Experience: 7-10 years

Education: Master’s Degree in Pharmacy or Biochemistry

Employment Type: Full-time

Industry: Healthcare & Life Sciences

Department: Quality Control & Compliance

Vacancies: 1

Company Overview

Sanofi is a global healthcare leader dedicated to chasing the miracles of science to improve people’s lives. With a presence in over 100 countries, we focus on transforming the practice of medicine through innovative research and development. Our commitment to global health is evident in our extensive portfolio of vaccines, specialty care, and general medicines. As we expand our operational footprint in West Africa, we are investing heavily in local infrastructure to ensure that life-saving medications are produced and distributed under the highest safety standards. We believe that health is a fundamental right, and our mission is to provide equitable access to healthcare solutions across the globe. By joining our team, you become part of a legacy of scientific excellence and a future focused on sustainable health outcomes. We prioritize diversity, inclusion, and a culture of continuous learning, ensuring that every employee has the tools to excel and innovate in a fast-paced environment. Our operations in Senegal are designed to integrate global best practices with local expertise to serve the regional population effectively.

Job Overview

We are currently seeking a highly skilled Pharmaceutical Quality Assurance Manager to lead our compliance and quality operations in Louga. This is a critical role designed to ensure that every product leaving our facility meets stringent international and national regulatory standards. The successful candidate will be responsible for overseeing the entire quality management system (QMS), managing audits, and leading a team of quality specialists. This position is ideal for a professional who is passionate about patient safety and operational excellence. As part of our growth strategy, this role offers significant career opportunities in Senegal for those looking to make a tangible impact on public health. You will act as the primary liaison between the production plant and regulatory bodies, ensuring that all Good Manufacturing Practices (GMP) are strictly adhered to. This role requires a blend of technical expertise, leadership skills, and a meticulous eye for detail to prevent deviations and ensure product efficacy.

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The Pharmaceutical Quality Assurance Manager will drive the culture of quality across the organization, promoting a proactive approach to risk management. By implementing robust monitoring systems and validation protocols, you will help Sanofi maintain its reputation as a trusted provider of healthcare solutions. This job vacancy in Senegal represents a unique chance to lead a specialized department in a region with rapidly growing pharmaceutical needs. We are looking for a leader who can balance the pressures of production deadlines with the uncompromising requirements of pharmaceutical safety.

Key Responsibilities

• Develop and implement comprehensive Quality Management Systems (QMS) in accordance with WHO and EMA guidelines.
• Oversee the review and approval of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
• Lead internal and external audits, ensuring all non-conformities are addressed through effective Corrective and Preventive Actions (CAPA).
• Manage the stability testing programs and environmental monitoring of cleanroom facilities.
• Coordinate with the production department to validate new equipment and manufacturing processes.
• Provide technical guidance and training to staff on Good Documentation Practices (GDP).
• Monitor supplier quality and conduct audits of raw material providers to ensure supply chain integrity.

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Required Skills

• Expert knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Strong proficiency in risk assessment methodologies such as FMEA.
• Advanced leadership and team management capabilities.
• Excellent analytical skills with the ability to interpret complex chemical and biological data.
• Fluency in French and English is mandatory for international reporting.
• Exceptional organizational skills and the ability to manage multiple regulatory deadlines.

Education

Candidates must possess a Master’s Degree in Pharmacy, Biochemistry, Chemistry, or a related Life Sciences field from a recognized university. Specialized certifications in Quality Management (e.g., Six Sigma or ISO 9001) are highly desirable and will be considered a significant advantage during the selection process.

Experience

A minimum of 7 to 10 years of professional experience in the pharmaceutical industry is required, with at least 3 years in a managerial or supervisory capacity within a Quality Assurance department. Proven experience in handling regulatory inspections and implementing CAPA systems is essential for success in this role.

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Benefits

• Competitive international salary package with performance-based bonuses.
• Comprehensive health, dental, and vision insurance for the employee and dependents.
• Relocation assistance and housing allowance for candidates moving to Louga.
• Generous annual leave and paid time off.
• Contribution to a private pension fund.

Training

• Advanced certification in Global Regulatory Affairs.
• Leadership development programs hosted at Sanofi’s international hubs.
• Specialized training on the latest pharmaceutical automation and digitalization tools.
• Continuous professional development in pharmacovigilance.

Working Environment

The working environment is a blend of a high-tech laboratory and a corporate office. The manager will spend significant time on the production floor ensuring compliance and in the office managing documentation. We foster a culture of precision, safety, and mutual respect. Employment in Senegal with Sanofi means working in a multicultural environment where scientific rigor is celebrated and innovation is encouraged.

Application Process

Interested candidates should submit their updated CV and a detailed cover letter outlining their experience with GMP and QMS. All applications will be screened for technical eligibility. Shortlisted candidates will undergo a three-stage interview process: a technical screening, a leadership assessment, and a final interview with the Regional Director. We are currently hiring in Senegal and encourage all qualified professionals to apply promptly.

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 race, religion, gender, age, or disability. We encourage women and underrepresented groups to apply for this position to help us build a more diverse scientific community.