Quality Assurance Manager Job Vacancy in Sidi Bouzid, Tunisia – Pharmaceuticals

Job Description

Position: Quality Assurance Manager

Company: Sanofi Tunisia

Location: Sidi Bouzid, Tunisia

Experience: 5+ years in pharmaceutical quality assurance

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

Employment Type: Full-time

Industry: Pharmaceuticals

Department: Quality Assurance

Salary: 3,000 – 5,000 SSP per month

Vacancies:1

Company Overview

Sanofi Tunisia is a leading global healthcare company dedicated to improving lives through innovative medicines, vaccines, and consumer healthcare products. With a strong presence across North Africa, Sanofi operates state‑of‑the‑art manufacturing facilities, research centers, and a robust distribution network that supports the health needs of millions. The company’s commitment to quality, sustainability, and employee development makes it an attractive employer for professionals seeking meaningful career opportunities in Tunisia. As part of Sanofi’s worldwide network, the Sidi Bouzid site plays a critical role in producing high‑quality pharmaceutical products for both local and export markets, reinforcing the company’s reputation for excellence.

Job Overview

The Quality Assurance Manager will lead the QA team at the Sidi Bouzid manufacturing plant, ensuring that all products meet stringent regulatory standards and internal quality specifications. This role involves overseeing the implementation of Good Manufacturing Practices (GMP), managing audits, and driving continuous improvement initiatives. The successful candidate will collaborate closely with production, engineering, and regulatory affairs to maintain the highest levels of product integrity. For more information about career opportunities in Tunisia, visit Tunisia Job Search. This position offers a unique chance to contribute to the health of the nation while advancing your professional growth.

Key Responsibilities

• Develop, implement, and maintain the Quality Management System (QMS) in compliance with GMP, WHO, and local regulatory requirements.
• Lead internal and external audits, including FDA, EMA, and Tunisian National Agency for Drug Control (ANMD) inspections.
• Oversee release testing, stability studies, and batch record reviews to ensure product compliance.
• Manage deviation investigations, root cause analysis, and corrective and preventive actions (CAPA).
• Coordinate cross‑functional teams to resolve quality issues and drive process improvements.
• Train and mentor QA staff on best practices, SOPs, and regulatory updates.
• Maintain documentation integrity, ensuring accurate and timely record keeping.
• Monitor key quality metrics and generate performance reports for senior management.
• Support new product introductions by reviewing specifications, validation protocols, and risk assessments.
• Ensure supplier qualification and ongoing monitoring of raw material quality.

Required Skills

• In‑depth knowledge of GMP, ISO 9001, and pharmaceutical quality standards.
• Strong analytical and problem‑solving abilities with a data‑driven mindset.
• Excellent communication and leadership skills to manage multidisciplinary teams.
• Proficiency in quality management software and Microsoft Office Suite.
• Ability to handle multiple projects simultaneously while meeting strict deadlines.
• Fluency in French and English; Arabic is a plus.

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 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, with at least two years in a supervisory or managerial role. Experience in a regulated manufacturing environment, familiarity with audit processes, and a proven track record of implementing continuous improvement initiatives are essential.

Salary

The compensation package ranges from 3,000 to 5,000 SSP per month, commensurate with experience and qualifications. The package includes performance‑based bonuses, health insurance, and a retirement savings plan.

Benefits

• Comprehensive medical, dental, and vision coverage.
• Generous paid time off and public holiday schedule.
• Professional development allowance and tuition reimbursement.
• Employee assistance program and wellness initiatives.
• Transportation subsidy for commuting to the Sidi Bouzid facility.

Training

• Onboarding program covering Sanofi’s QMS, safety protocols, and corporate culture.
• Continuous training in regulatory updates, advanced QA methodologies, and leadership development.
• Access to internal e‑learning platforms and external certification courses.

Working Environment

Sanofi Tunisia offers a collaborative, inclusive, and safety‑focused workplace. The Sidi Bouzid plant features modern laboratories, controlled manufacturing zones, and state‑of‑the‑art equipment. Employees benefit from a supportive culture that encourages innovation, knowledge sharing, 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 the Sanofi Careers 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 Tunisia is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of gender, age, disability, race, religion, or sexual orientation. All qualified applicants will receive consideration for employment without regard to any protected characteristic.