Regulatory Affairs Specialist Job Vacancy in Mbeya, Tanzania – Pharmaceuticals

API Integration Specialist
Mbeya
September 19, 2026
Full Time
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Job Description

Position:Regulatory Affairs Specialist

Company:Pfizer Tanzania

Location:Mbeya, Tanzania

Experience:3-5 years in pharmaceutical regulatory affairs

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

Employment Type:Full-time

Industry:Pharmaceuticals

Department:Regulatory Affairs

Salary:SSP 2,500,000 – SSP 3,500,000 per month

Vacancies:1

Company Overview

Pfizer Tanzania is a leading global biopharmaceutical company dedicated to improving health outcomes across the continent. With a strong presence in Tanzania for over two decades, Pfizer delivers innovative medicines, vaccines, and consumer health products that address critical health challenges. The company operates state‑of‑the‑art manufacturing and distribution facilities, collaborates with local health authorities, and invests in community health programs. As part of its commitment to excellence, Pfizer Tanzania continuously seeks talented professionals to drive regulatory compliance, scientific innovation, and market access, making it a top destination for Tanzania Jobs and career growth.

Job Overview

The Regulatory Affairs Specialist will serve as the primary liaison between Pfizer Tanzania and national regulatory bodies, ensuring that all products meet the stringent requirements of the Tanzania Food and Drugs Authority (TFDA). This role involves preparing and submitting dossiers, managing product registrations, and providing strategic guidance on regulatory pathways. The specialist will work closely with cross‑functional teams, including Clinical Development, Quality Assurance, and Marketing, to support the launch and lifecycle management of pharmaceutical products. For more information about Pfizer’s mission and values, visit the main website at https://tanzaniajobsearch.com/. This position offers a unique opportunity to contribute to the health of Tanzanians while advancing your professional expertise in a dynamic, multinational environment.

Key Responsibilities

  • Prepare, compile, and submit regulatory dossiers for new drug applications, variations, and renewals in compliance with TFDA guidelines.
  • Maintain an up‑to‑date regulatory intelligence database, monitoring changes in local and regional legislation.
  • Coordinate with internal stakeholders to gather scientific data, labeling, and packaging information required for submissions.
  • Act as the primary point of contact with TFDA officials, responding to queries and facilitating inspections.
  • Develop and implement regulatory strategies that align with business objectives and market access goals.
  • Provide regulatory training and guidance to project teams to ensure adherence to compliance standards.
  • Support post‑marketing surveillance activities, including adverse event reporting and product recalls.

Required Skills

  • In‑depth knowledge of Tanzanian pharmaceutical regulations and international guidelines (ICH, WHO).
  • Excellent written and verbal communication skills in English and Swahili.
  • Strong analytical and problem‑solving abilities with attention to detail.
  • Proficiency in regulatory submission software and document management systems.
  • Ability to work collaboratively across multidisciplinary teams.
  • Project management experience with the capacity to meet tight deadlines.

Education

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

Experience

Applicants must have a minimum of three to five years of hands‑on experience in regulatory affairs within the pharmaceutical industry, preferably with exposure to the Tanzanian market. Experience with product registration, lifecycle management, and interaction with health authorities is essential.

Salary

The successful candidate will receive a competitive monthly salary ranging from SSP 2,500,000 to SSP 3,500,000, commensurate with experience and qualifications. Additional performance‑based incentives may be offered.

Benefits

  • Comprehensive health insurance for employee and dependents.
  • Retirement savings plan with employer contributions.
  • Generous paid leave, including annual, sick, and parental leave.
  • Employee assistance program and wellness initiatives.
  • Opportunities for international assignments and career advancement.

Training

  • Continuous professional development through internal and external regulatory workshops.
  • Access to Pfizer’s global e‑learning platform for skill enhancement.
  • Mentorship program with senior regulatory leaders.
  • Support for obtaining regulatory certifications and advanced degrees.

Working Environment

Pfizer Tanzania offers a collaborative, inclusive, and innovative workplace located in the vibrant city of Mbeya. The office environment promotes teamwork, knowledge sharing, and a strong focus on employee well‑being. Modern facilities, flexible working arrangements, and a culture that values diversity make this an ideal setting for professionals seeking meaningful impact and career growth.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining their relevant experience through the online portal on our website. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for interviews. Please ensure all documents are in PDF format and clearly labeled.

Equal Opportunity Statement

Pfizer Tanzania 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, or sexual orientation. Our hiring practices reflect our dedication to fairness and the belief that diverse perspectives drive innovation and success.

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