DEADLINE: 24/01/2025
Lead-Regulatory Affairs
Full-time
The Lead-Regulatory Affairs will be managing all regulatory activities, support product transfer and formulation development processes, review product life cycle management applications, marketing authorization applications, and approval of packaging material artworks.
We seek to recruit a dynamic, competent, experienced, and professionally confident individual, who is also a committed team player to strengthen our staff capacity.
Job Role: LEAD-REGULATORY AFFAIRS
Section/Department:REGULATORY AFFAIRS
Requirements:
- Bachelor’s degree in Pharmacy
- Masters in any related field will be an added advantage
- Registered Pharmacist with 5+ years of experience in a Regulatory Affairs role within in a pharmaceutical industry of which 2 years should be at supervisory level
- Sufficient knowledge of regulatory regulations, standards and guidelines
- Ability to work independently and collaboratively within a team
- Ability to work under pressure and to deliver on the set deadlines
- Ability to adhere to GMP and Quality Management Systems
- High analytical mind, with exceptional problem-solving skills and attention to detail
- Self-starter, flexible and with excellent communication skills, both oral and written
- Proficiency in MS Office (Excel, PowerPoint presentations)
How to Apply
Email your application, detailed CV and copies of academic certificates in a PDF file to;
[email protected] by 24th January 2025.
Only short-listed candidates will be contacted.

About Quality Chemicals Limited
Industry: Management
Location: Kampala, Uganda
Qcil is a publicly listed pharmaceutical manufacturing company, established in Uganda by Ugandans in 2005. The Company is committed to advancing wellness and is the largest producer of WHO pre-qualified HIV/AIDS and Malaria treatments in the region.
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