Regulatory Affairs Specialist Job Vacancy in Beau Bassin, Mauritius – Pharmaceuticals

Job Description

Position: Regulatory Affairs Specialist

Company: GlaxoSmithKline (GSK)

Location: Beau Bassin, Mauritius

Experience: 5+ years in regulatory affairs within pharmaceutical industry

Education: Bachelor’s degree in Pharmacy, Life Sciences or related field; Master’s preferred

Employment Type: Full-time

Industry: Pharmaceuticals

Department: Regulatory Affairs

Salary: SSP 800,000 – SSP 1,200,000 per annum

Vacancies:1

Company Overview

GlaxoSmithKline (GSK) is a global healthcare leader dedicated to improving the quality of life through innovative medicines, vaccines, and consumer healthcare products. With a strong presence in Mauritius, GSK combines cutting‑edge research with local market expertise to deliver high‑quality pharmaceutical solutions across the island and the broader African region. As part of its commitment to excellence, GSK continuously invests in talent development, sustainability, and community health initiatives, making it a premier employer for professionals seeking meaningful career opportunities. This role contributes directly to GSK’s mission of delivering safe, effective, and compliant products, reinforcing the company’s reputation as a trusted partner in the pharmaceutical sector. The position also supports GSK’s strategic objectives of expanding market access, ensuring regulatory compliance, and fostering innovation in a dynamic regulatory environment. By joining GSK, you become part of a diverse, inclusive, and forward‑thinking team that values collaboration, integrity, and scientific excellence.

Job Overview

The Regulatory Affairs Specialist will be responsible for managing the end‑to‑end regulatory lifecycle of GSK’s pharmaceutical portfolio in Mauritius and the surrounding region. This includes preparing and submitting dossiers, liaising with the Mauritius Medicines Authority, and ensuring that all products meet local and international regulatory standards. The role demands a proactive approach to monitoring legislative changes, providing strategic guidance to cross‑functional teams, and maintaining robust documentation. As a key member of the Regulatory Affairs department, you will work closely with Quality Assurance, Clinical Development, and Commercial teams to facilitate timely product launches and sustain market presence. For more information about GSK’s career opportunities, visit Mauritius Job Search. This position offers a unique platform to influence public health outcomes while advancing your professional growth within a globally recognized organization.

Key Responsibilities

• Prepare, review, and submit regulatory dossiers for new drug applications, variations, and renewals in compliance with Mauritius Medicines Authority guidelines.
• Maintain up‑to‑date knowledge of local and international pharmaceutical regulations, including ICH, WHO, and EU directives.
• Collaborate with cross‑functional teams to ensure product labeling, packaging, and promotional materials meet regulatory requirements.
• Provide regulatory strategy input for product development, clinical trials, and post‑marketing activities.
• Monitor and assess regulatory changes, advising senior management on potential impact and mitigation strategies.
• Manage timelines and documentation for all regulatory submissions, ensuring accuracy and completeness.
• Act as the primary point of contact with the Mauritius Medicines Authority and other health agencies.
• Support internal audits and inspections by preparing necessary documentation and responding to queries.
• Develop and maintain a regulatory intelligence database to support continuous improvement.
• Contribute to the preparation of risk assessments, safety reports, and pharmacovigilance submissions as required.

Required Skills

• In‑depth understanding of pharmaceutical regulatory frameworks in Mauritius and internationally.
• Excellent written and verbal communication skills, with the ability to convey complex regulatory concepts clearly.
• Strong analytical and problem‑solving abilities, capable of interpreting scientific data and regulatory guidelines.
• Proficiency in regulatory submission software and document management systems.
• Attention to detail and high level of accuracy in documentation.
• Ability to work collaboratively in multidisciplinary teams and manage multiple projects simultaneously.
• Negotiation and stakeholder management skills for effective liaison with authorities.
• Proactive mindset with a commitment to continuous learning and professional development.

Education

A Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline is required. A Master’s degree or professional certification (e.g., RAC, RAPS) is highly desirable and will be considered an advantage during the selection process.

Experience

Minimum of five (5) years of hands‑on experience in regulatory affairs within the pharmaceutical industry, preferably with exposure to both local and international submissions. Experience working with the Mauritius Medicines Authority or similar regulatory bodies is strongly preferred.

Salary

The competitive remuneration package ranges from SSP 800,000 to SSP 1,200,000 per annum, commensurate with experience and qualifications. The package includes performance‑based bonuses, health insurance, and a comprehensive retirement plan.

Benefits

• Comprehensive medical, dental, and vision coverage.
• Generous paid time off and statutory holidays.
• Retirement savings scheme with employer contributions.
• Employee assistance program and wellness initiatives.
• Professional development allowance and tuition reimbursement.
• Employee discount programs for GSK products.

Training

• On‑boarding program covering GSK’s regulatory processes, compliance standards, and corporate culture.
• Continuous learning opportunities through internal workshops, external conferences, and e‑learning platforms.
• Mentorship from senior regulatory leaders to accelerate career progression.
• Access to GSK’s global knowledge network for best practice sharing.

Working Environment

GSK offers a modern, collaborative workplace located in Beau Bassin, equipped with state‑of‑the‑art facilities and flexible working arrangements. The culture promotes innovation, diversity, and a strong sense of purpose, encouraging employees to bring their authentic selves to work while contributing to impactful health solutions.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining relevant experience through the online portal on the GSK Careers page. 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

GlaxoSmithKline is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of gender, race, religion, age, disability, sexual orientation, or any other protected characteristic. All qualified applicants will receive consideration for employment without discrimination.