Pharmaceutical Quality Assurance Auditor Job Vacancy in Mbacké, Senegal – Pharmaceutical Manufacturing

Job Description

Position: Pharmaceutical Quality Assurance Auditor

Company: Sanofi

Location: Mbacké, Senegal

Experience: 5-8 years in pharmaceutical quality assurance, auditing, or regulatory compliance

Education: Bachelor’s Degree in Pharmacy, Chemistry, or related Life Sciences field

Employment Type: Full-time

Industry: Pharmaceutical Manufacturing

Department: Quality Assurance & Regulatory Compliance

Vacancies:1

Company Overview

Sanofi is a leading global biopharmaceutical company dedicated to supporting people through their health challenges. We are an innovative global healthcare company, driven by one purpose: we chase the miracles of science to improve people’s lives. Our team, across some 100 countries, is dedicated to transforming the practice of medicine by working to turn the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the center of our ambitions. In Senegal, Sanofi has established a significant manufacturing and distribution presence, contributing to the local healthcare ecosystem and creating numerous career opportunities in Senegal. Our commitment to quality, patient safety, and regulatory excellence is unwavering, making us a trusted partner in public health across West Africa.

Job Overview

We are seeking a meticulous and experienced Pharmaceutical Quality Assurance Auditor to join our team in Mbacké. This critical role is responsible for ensuring that all manufacturing, testing, and distribution activities comply with Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), and other relevant regulatory standards set by authorities such as the Senegalese Ministry of Health and the World Health Organization (WHO). The successful candidate will be a key player in maintaining the integrity of our quality management system, conducting internal and external audits, and driving continuous improvement initiatives. This position offers a unique job vacancy in Senegal for a professional passionate about quality and patient safety within a world-class pharmaceutical environment. For more jobs in Senegal, visit https://senegaljobsearch.com.

Key Responsibilities

• Plan, schedule, and conduct comprehensive internal audits of manufacturing, packaging, labeling, warehouse, and quality control operations to ensure compliance with cGMP, GDP, and company standards.
• Manage and execute supplier qualification audits for critical raw material vendors, contract manufacturers, and third-party logistics providers.
• Prepare detailed audit reports, documenting observations, deviations, and non-conformities, and present findings to site management and quality leadership.
• Track and verify the timely and effective closure of audit corrective and preventive actions (CAPAs).
• Support regulatory inspections by health authorities, including preparation, hosting, and follow-up on inspection observations.
• Review and approve quality-related documentation, including batch records, validation protocols, and standard operating procedures (SOPs).
• Participate in risk assessment activities and contribute to the site’s quality management review process.
• Stay abreast of evolving local and international regulatory requirements and industry best practices.
• Provide quality assurance guidance and training to operational staff to foster a strong quality culture.
• Investigate quality incidents and product complaints to determine root cause and implement effective corrective actions.

Required Skills

• In-depth knowledge of current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP), and relevant ICH guidelines.
• Proven experience in conducting pharmaceutical quality audits and managing audit programs.
• Strong analytical, problem-solving, and root cause analysis skills.
• Excellent written and verbal communication skills, with the ability to write clear, concise, and factual audit reports.
• High level of integrity, attention to detail, and a proactive, risk-based approach to quality.
• Ability to work independently, manage multiple priorities, and influence stakeholders at various levels.
• Proficiency in quality management systems (QMS) and documentation software.
• Fluency in French (required) and professional working proficiency in English.

Education

A minimum of a Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biochemistry, or a related Life Sciences field is required. A Master’s degree or additional certifications in Quality Assurance or Auditing (e.g., Certified Quality Auditor) is a significant advantage.

Experience

A minimum of 5 to 8 years of hands-on experience in a quality assurance role within the pharmaceutical or biotech manufacturing industry, with at least 3 years specifically focused on conducting internal and external quality audits. Direct experience with regulatory inspections is essential.

Benefits

• Competitive salary and performance-based annual bonus.
• Comprehensive health, dental, and life insurance coverage.
• Retirement savings plan with company contribution.
• Continuous professional development and training opportunities.
• Paid time off and annual leave in accordance with local regulations.
• Opportunities for career progression within a global organization.
• Employee assistance and wellness programs.

Training

• Extensive onboarding program covering Sanofi’s global quality policies and procedures.
• Specialized training in advanced auditing techniques and regulatory intelligence.
• Access to global Sanofi quality networks and best practice sharing forums.
• Ongoing training on new regulatory requirements and quality management systems.

Working Environment

You will be based at our modern pharmaceutical manufacturing facility in Mbacké, working within a dynamic and collaborative Quality Assurance team. The role involves a mix of office-based work and time on the manufacturing floor and in warehouses. The environment is fast-paced, requiring a high degree of precision and adherence to strict protocols. We foster a culture of safety, quality, and continuous improvement, where every team member’s contribution is valued in our mission to deliver high-quality medicines. This role represents a premier opportunity for employment in Senegal in the vital pharmaceutical sector.

Application Process

Qualified candidates are invited to submit their updated CV and a cover letter through our official careers portal. The recruitment process will include an initial screening, followed by interviews with the Quality Assurance Manager and the Site Head of Quality. Selected candidates may also be asked to complete a practical assessment. We thank all applicants for their interest; however, only those selected for an interview will be contacted. For other Senegal jobs and regional opportunities, you can explore https://www.tunisiajobsearch.com/.

Equal Opportunity Statement

Sanofi is proud to be an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for hiring in Senegal without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. We believe a diverse workforce drives innovation and allows us to better serve our patients and communities.