Company: Biodeal Laboratories
Location: Nairobi, Kenya
Application Deadline: 10th March 2026

About the Role

Are you a registered Pharmacist looking to build your career in pharmaceutical manufacturing?

Biodeal Laboratories is seeking five (5) motivated and growth-oriented Pharmacists to join our team in Nairobi across Quality Assurance, Regulatory Affairs, and GMP Operations.

This is an excellent opportunity to gain hands-on experience within a WHO-GMP compliant manufacturing environment, deepen your technical expertise, and contribute to the production of safe, effective, and high-quality medicines serving Kenya and the wider region.

Key Responsibilities

Depending on functional placement (Quality, Regulatory, or GMP), responsibilities may include:

Quality Assurance / Quality Control

• Support implementation and maintenance of Quality Management Systems (QMS).

• Review batch manufacturing records and ensure compliance with GMP standards.

• Participate in internal audits, deviations, CAPA management, and change control processes.

• Ensure proper documentation and record integrity in line with regulatory requirements.

Regulatory Affairs

• Assist in preparation and submission of regulatory dossiers.

• Maintain product registrations and variations with regulatory authorities.

• Monitor regulatory updates and ensure company compliance with local and regional requirements.

• Liaise with regulatory bodies and internal technical teams.

GMP Operations / Production Oversight

• Ensure compliance with WHO-GMP guidelines in manufacturing processes.

• Monitor production activities to ensure adherence to SOPs and quality standards.

• Support validation, qualification, and continuous improvement initiatives.

• Promote a strong culture of quality and compliance within operations.

Qualifications & Requirements

• Bachelor of Pharmacy (BPharm) degree from a recognized institution.

• Registered Pharmacist with a valid practicing license in Kenya.

• Strong interest in pharmaceutical manufacturing, quality systems, or regulatory affairs.

• High level of integrity, attention to detail, and documentation discipline.

• Ability to work in a structured, compliance-driven environment.

• Strong analytical, organizational, and communication skills.

What You Will Gain

• Hands-on exposure in a WHO-GMP manufacturing environment.

• Practical experience in Quality, Regulatory, and GMP systems.

• Career development within a growing local pharmaceutical manufacturer.

• Opportunity to contribute to strengthening regional pharmaceutical manufacturing capacity.

How to Apply

Qualified and interested candidates are invited to submit their CV to:
📩 hr@biodealkenya.com

Deadline: 10th March 2026