Quality Assurance Manager at Dawa Life Sciences

October 1, 2026

Job Overview

  • Date Posted
    October 1, 2026
  • Location
  • Expiration date
    November 30, 2026
  • Experience
    3 Years
  • Gender
    Both
  • Qualification
    Bachelor Degree

Job Description

Brief Job Description:

  • Leading, maintaining and continuously improving the Quality Management System (QMS) in line with international cGMP, GDP and GSP standards
  • Acting as a registered Company Pharmacist, fulfilling all legal and regulatory responsibilities of the role, including the release of finished pharmaceutical products to the market
  • Ensuring that all processes, specifications, instructions and results comply with the registered dossiers and with national and international GMP, GSP and GDP regulations
  • Authorizing written procedures and their amendments, including SOPs, cleaning and operating procedures, specifications, analytical methods, validation/qualification and stability protocols, and batch and packaging instructions and records
  • Managing, reviewing and approving the calibration and qualification of equipment, instruments, facilities and utilities, and the validation of manufacturing processes and cleaning procedures
  • Reviewing batch records, packaging records and analytical testing records, and approving or rejecting starting materials, packaging materials, intermediates, bulk and finished products
  • Qualifying, approving and monitoring manufacturers of raw materials, intermediates, packaging materials and finished products, and participating in external audits of vendors and service providers
  • Conducting regular self-inspections and internal audits, managing inspections by authorities and customers, and ensuring timely closure of resulting CAPAs
  • Managing, investigating and closing market complaints and managing product recalls, ensuring timely response to customers and regulatory authorities
  • Ensuring timely preparation, review and approval of Product Quality Review (PQR) reports
  • Preparing, executing, controlling and monitoring the Quality Assurance CAPEX and OPEX budget
  • Acting as the back-up QPPV in the absence of the QPPV
  • Leading and developing the Quality Assurance team
    • Providing functional and disciplinary leadership
    • Ensuring regular and effective cGMP and GDP training of all staff
    • Promoting a strong quality culture across pharmaceutical operations

Qualifications and Experience:
Must Have: Minimum Requirements
To be considered, these minimum requirements must be evident on your resume.

  • Education: Bachelor of Pharmacy degree
  • Registered as a Pharmacist in the Republic of Kenya
  • A minimum of 5 years’ experience in the Pharmaceutical Industry, of which at least 3 years should be in a similar position
  • Expert understanding of local and international regulations and standards for cGMP, GDP and GSP
  • Excellent leadership, reporting and organizational skills, with the ability to design procedures and influence as a team player
  • Self-driven and structured, able to work under minimal supervision, resolve problems in a timely manner and handle high work pressure
  • Proficient computer skills: MS Word, MS Excel and MS PowerPoint; proficiency in English