Pharmaceutical Manufacturing Quality Engineer Job Vacancy in Sousse, Tunisia – Pharmaceuticals

Job Description

Position: Pharmaceutical Manufacturing Quality Engineer

Company: Novartis

Location: Sousse, Tunisia

Experience: 3-5 years

Education: Bachelor’s degree in Pharmaceutical Sciences or Engineering

Employment Type: Full-time

Industry: Pharmaceuticals

Department: Quality Assurance

Salary: 3,500 – 5,000 SSP per month

Vacancies:1

Company Overview

Novartis is a global leader in innovative medicines, vaccines, and consumer health products, operating in more than 150 countries. With a strong commitment to research and development, Novartis continuously invests in cutting‑edge technologies to improve patient outcomes and enhance the quality of life worldwide. In Tunisia, Novartis has established a state‑of‑the‑art manufacturing hub in Sousse, supporting the regional supply chain for a wide portfolio of pharmaceutical products. The company’s core values—innovation, quality, collaboration, and integrity—drive every aspect of its operations, creating a dynamic environment where professionals can grow, contribute, and make a tangible impact on health care across the continent. As part of its strategic expansion, Novartis is actively seeking talented individuals who share a passion for excellence and a desire to be part of a world‑class team dedicated to delivering safe, effective, and high‑quality medicines.

Working at Novartis in Tunisia offers a unique blend of global standards and local expertise. Employees benefit from comprehensive training programs, competitive compensation, and a supportive culture that encourages continuous learning and career progression. The Sousse facility is recognized for its adherence to Good Manufacturing Practices (GMP) and its commitment to sustainability, making it an attractive destination for professionals seeking meaningful career opportunities in the pharmaceutical sector.

Job Overview

The Pharmaceutical Manufacturing Quality Engineer will play a pivotal role in ensuring that all products manufactured at the Sousse site meet the highest standards of quality, safety, and regulatory compliance. This position involves close collaboration with cross‑functional teams, including Production, Validation, Regulatory Affairs, and Supply Chain, to develop, implement, and maintain robust quality systems. The engineer will be responsible for monitoring manufacturing processes, conducting risk assessments, and driving continuous improvement initiatives that align with Novartis’s global quality strategy. This role offers an exciting opportunity to contribute to the delivery of life‑saving medicines while advancing your professional expertise in a fast‑paced, innovative environment.

For more information about Novartis career opportunities, visit the company’s global careers portal: https://www.novartis.com/careers.

Explore additional resources on the Tunisian job market and discover other exciting openings at our partner platform: https://tunisiajobsearch.com.

Key Responsibilities

• Develop, implement, and maintain quality engineering procedures in accordance with GMP, ISO 9001, and Novartis internal standards.
• Perform root‑cause investigations for deviations, non‑conformances, and out‑of‑specification results, and lead corrective and preventive actions (CAPA).
• Collaborate with Production and Validation teams to design and execute process validation protocols, including IQ/OQ/PQ activities.
• Conduct risk assessments using tools such as FMEA and HACCP to identify potential quality issues and propose mitigation strategies.
• Monitor key performance indicators (KPIs) related to product quality, batch release, and process stability, and generate regular reports for senior management.
• Support internal and external audits, ensuring readiness for regulatory inspections by agencies such as the Tunisian Ministry of Health and the European Medicines Agency.
• Lead continuous improvement projects focused on reducing variability, enhancing efficiency, and increasing overall product quality.
• Provide technical training and mentorship to manufacturing staff on quality best practices and compliance requirements.

Required Skills

• Strong knowledge of GMP, FDA, EMA, and local Tunisian regulatory requirements for pharmaceutical manufacturing.
• Proficiency in statistical analysis tools (e.g., Minitab, JMP) and quality management software.
• Excellent problem‑solving abilities with a data‑driven approach to decision making.
• Effective communication skills in both French and English; Arabic is a plus.
• Ability to work collaboratively in multidisciplinary teams and influence stakeholders at all levels.
• Project management experience, including planning, execution, and documentation.

Education

A minimum of a Bachelor’s degree in Pharmaceutical Sciences, Chemical Engineering, Biotechnology, or a related field is required. A Master’s degree or professional certifications such as CQE (Certified Quality Engineer) or Six Sigma Green Belt are highly desirable and will be considered an advantage during the selection process.

Experience

Applicants should have 3 to 5 years of hands‑on experience in quality engineering or quality assurance within a regulated pharmaceutical manufacturing environment. Experience with technology transfer, process validation, and audit support is essential. Prior exposure to multinational pharmaceutical companies or contract manufacturing organizations (CMOs) will be viewed favorably.

Salary

The compensation package ranges from 3,500 to 5,000 SSP per month, commensurate with experience, qualifications, and performance. In addition to the base salary, Novartis offers performance‑based bonuses, health insurance, retirement benefits, and a range of employee wellness programs.

Benefits

• Comprehensive health and dental coverage for employees and dependents.
• Retirement savings plan with company matching contributions.
• Generous paid time off, including vacation, sick leave, and public holidays.
• Professional development budget for certifications, conferences, and advanced training.
• Employee assistance program and wellness initiatives.
• Relocation assistance for candidates moving to Sousse.

Training

• Onboarding program covering Novartis quality systems, GMP fundamentals, and site‑specific procedures.
• Continuous learning modules on advanced analytics, risk management, and regulatory updates.
• Mentorship pairing with senior quality leaders to accelerate skill development.
• Access to Novartis University for online courses and certifications.

Working Environment

Novartis provides a modern, safety‑focused manufacturing environment equipped with cutting‑edge technology and robust quality infrastructure. The Sousse site adheres to strict environmental and safety standards, fostering a culture of responsibility and continuous improvement. Employees enjoy a collaborative atmosphere where ideas are welcomed, and innovation is rewarded. The company promotes work‑life balance through flexible scheduling options and supportive management practices.

Application Process

Interested candidates are invited to submit their updated CV and a cover letter outlining their relevant experience through the Novartis online career portal. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for an initial virtual interview followed by on‑site assessments.

Equal Opportunity Statement

Novartis is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or veteran status.