Pharmaceutical Quality Assurance Manager Job Vacancy in Kédougou, Senegal – Pharmaceutical Manufacturing

Job Description

Position: Pharmaceutical Quality Assurance Manager

Company: Sanofi

Location: Kédougou, Senegal

Experience: 7+ years in pharmaceutical quality assurance or quality control

Education: Master’s degree in Pharmacy, Chemistry, or related field

Employment Type: Full-time

Industry: Pharmaceutical Manufacturing

Department: Quality Assurance

Vacancies:1

Company Overview

Sanofi is a global biopharmaceutical company focused on human health, committed to preventing illness with vaccines and providing innovative treatments. With a presence in over 100 countries, Sanofi is dedicated to supporting the health and well-being of communities worldwide. In Senegal, Sanofi has established a significant manufacturing and distribution footprint, contributing to the local pharmaceutical ecosystem and ensuring access to essential medicines. Our Kédougou facility represents a state-of-the-art manufacturing plant adhering to the highest international quality standards, including Good Manufacturing Practices (GMP) and World Health Organization (WHO) guidelines. We are committed to sustainable development, local capacity building, and improving healthcare outcomes across West Africa. This role offers a unique opportunity to join a leading global healthcare company while making a tangible impact on public health in Senegal and the surrounding region.

Job Overview

We are seeking a highly experienced and detail-oriented Pharmaceutical Quality Assurance Manager to lead our quality assurance operations at the Sanofi manufacturing facility in Kédougou. This critical role is responsible for ensuring all pharmaceutical products manufactured at the site meet stringent regulatory requirements, internal quality standards, and patient safety expectations. The successful candidate will oversee the entire quality management system, manage a team of quality professionals, and serve as the primary point of contact for regulatory inspections. This position is central to maintaining our license to operate and our reputation for excellence in Senegal Jobs within the pharmaceutical sector. You will be at the forefront of implementing robust quality processes, driving continuous improvement initiatives, and fostering a culture of quality excellence throughout the organization. For more Jobs in Senegal and career resources, visit our partner site at https://senegaljobsearch.com.

Key Responsibilities

• Develop, implement, and maintain the site’s Quality Management System (QMS) in full compliance with local Senegalese regulations, international GMP standards, and Sanofi global policies.
• Lead and manage the Quality Assurance team, providing coaching, mentorship, and performance management to ensure a high-performing unit.
• Oversee all quality control activities, including batch record review, product release, stability studies, and environmental monitoring.
• Manage deviation investigations, corrective and preventive actions (CAPA), change controls, and product quality reviews to ensure timely and effective resolution of quality issues.
• Act as the site’s Management Representative for all regulatory agency interactions, including preparations for and hosting of inspections by the Senegalese Directorate of Pharmacy and Medicines (DPM) and other health authorities.
• Ensure the qualification and validation of facilities, equipment, utilities, and manufacturing processes are executed and documented according to validation master plans.
• Review and approve quality-related documents, including standard operating procedures (SOPs), specifications, master batch records, and validation protocols/reports.
• Manage supplier quality assurance, including the qualification of raw material suppliers and contract manufacturers.
• Monitor quality metrics and key performance indicators (KPIs) to track system performance and identify areas for improvement.
• Promote a strong quality culture across all departments through regular training and communication on quality principles and regulatory requirements.

Required Skills

• In-depth knowledge of pharmaceutical GMP regulations (WHO, EU, FDA) and Senegalese pharmaceutical laws.
• Proven leadership and people management skills with the ability to motivate and develop a technical team.
• Excellent analytical, problem-solving, and decision-making abilities, particularly in root cause analysis.
• Strong communication and interpersonal skills, with fluency in French (required) and professional proficiency in English.
• High level of integrity, ethics, and professional discretion.
• Proficiency in quality management software and MS Office applications.
• Ability to work effectively under pressure and manage multiple priorities in a dynamic manufacturing environment.
• Strong project management and organizational skills.

Education

A Master’s degree or higher in Pharmacy, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a closely related scientific field is required. Additional certifications in Quality Assurance (e.g., Certified Quality Auditor) are highly desirable.

Experience

A minimum of 7 years of progressive experience in pharmaceutical quality assurance or quality control within a GMP-regulated manufacturing environment. At least 3 years of experience in a managerial or supervisory role leading a QA/QC team is essential. Direct experience with regulatory inspections and audits is mandatory. Experience in solid dosage form manufacturing is a strong advantage.

Benefits

• Competitive salary package with performance-based bonuses.
• Comprehensive health, dental, and life insurance for employee and family.
• Retirement savings plan with company contribution.
• Generous annual leave and public holiday allowance.
• Continuous professional development and training opportunities.
• Relocation assistance for candidates moving to Kédougou.
• Company-sponsored wellness programs.

Training

• Extensive onboarding program covering Sanofi’s global quality systems and local procedures.
• Regular internal and external training on updated GMP regulations, quality risk management, and leadership development.
• Opportunities for international training and knowledge exchange with other Sanofi quality sites.
• Sponsorship for relevant professional certification courses.

Working Environment

You will work in a modern, climate-controlled pharmaceutical manufacturing facility in Kédougou, equipped with advanced technology. The role involves a combination of office work and time on the manufacturing floor. You will lead a dedicated team of quality professionals and collaborate closely with production, engineering, supply chain, and regulatory affairs departments. Sanofi promotes a culture of safety, quality, and innovation, offering a professional and supportive work environment. This is a premier Job Vacancy in Senegal for quality professionals seeking to advance their careers with a global leader.

Application Process

Qualified candidates are invited to submit a detailed CV and a cover letter outlining their suitability for the role through the Sanofi careers portal. The selection process will include a preliminary screening of applications, followed by interviews with the hiring manager and senior site leadership, and potentially a practical assessment. We encourage all eligible candidates to apply for this outstanding opportunity among Career Opportunities in Senegal. For additional resources on Employment in Senegal, you may also visit https://www.tunisiajobsearch.com/.

Equal Opportunity Statement

Sanofi is an equal opportunity employer committed to diversity and inclusion in the workplace. All qualified applicants will receive consideration for Hiring in Senegal without regard to race, color, religion, sex, national origin, disability status, or any other characteristic protected by law. We value the unique contributions of every individual and strive to create an environment where everyone can thrive.