Job Description
WE ARE HIRING!
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EXECUTIVE - REGULATORY AFFAIRS
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The Executive - Regulatory Affairs is responsible for ensuring that all products comply with regulatory requirements and that the organization’s regulatory activities are managed efficiently to achieve and maintain product registrations.
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KEY RESPONSIBILITIES
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n- Prepare, compile, submit, and follow up on product registration dossiers in accordance with regulatory requirements.
n- Coordinate and manage product registration, renewal, variation, and other regulatory submissions with the relevant regulatory authorities.
n- Liaise effectively with the National Medicines Regulatory Authority (NMRA) and other relevant government authorities to facilitate regulatory approvals.
n- Maintain accurate and up-to-date regulatory documentation, ensuring compliance with applicable pharmaceutical or Medical Devices regulations and company policies.
n- Monitor changes in regulatory requirements and ensure timely implementation to maintain product compliance.
n- Maintain regulatory databases and records, ensuring all licenses, approvals, and registrations remain current.
n- Provide regulatory support to internal stakeholders by addressing compliance-related queries and coordinating regulatory activities.
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QUALIFICATIONS & EXPERIENCE
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n- Bachelor's Degree in Pharmacy or an equivalent professional qualification.
n- Minimum of two (2) years of proven experience in Regulatory Affairs within the pharmaceutical or Medical Devices industry, preferably in a similar capacity.
n- Sound knowledge of pharmaceutical or Medical Devices regulatory requirements, guidelines, and submission processes.
n- Excellent communication, interpersonal, and organizational skills, with the ability to manage multiple tasks and meet deadlines.
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HOW TO APPLY
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Interested candidates are invited to submit their updated CV along with details of two non-related referees and expected salary to:
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Application Deadline: 18th September 2026
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Only shortlisted candidates will be contacted.