Head Quality Operations at Dei BioPharma

Location: Wakiso, Uganda

Deadline: 31st October 2025

Experience: 8–10 years in GMP-regulated pharmaceutical/biotech

Qualification: Bachelor’s in Pharmacy/Chemistry/Biochemistry (Master’s preferred)

About Dei BioPharma

Dei BioPharma Ltd is a biotech and pharmaceutical research firm duly incorporated in Uganda, specializing in the development and manufacture of innovative medicines and vaccines. Our state-of-the-art manufacturing facility, situated in Matugga, Wakiso district, Uganda, shall produce high-quality medicines across a wide range of therapeutic areas.

Job Summary

The Head of Quality Operations is responsible for Overseeing Quality Assurance and Quality Control Operations, Ensuring Compliance with GMP and Regulatory Standards, Developing and Implementing Quality Management Systems, Conducting Internal Audits and Inspections, Reviewing and Approving Validation Protocols and Documentation, and Leading Continuous Improvement Initiatives across all departments.

The work schedule for this position is: Full Time, 45 hours per week (Monday to Saturday).

Key Responsibilities

• Supervise and coordinate the activities of the Quality Assurance (QA) and Quality Control (QC) teams.
• Ensure compliance with GMP, GDP, and all applicable regulatory and company standards.
• Develop, implement, and maintain the Quality Management System (QMS) across all departments.
• Review, approve, and control Standard Operating Procedures (SOPs) and validation documents.
• Oversee product testing, batch release, and ensure proper documentation for each process.
• Plan and conduct internal quality audits and coordinate external audits and inspections.
• Investigate deviations, non-conformances, and implement effective corrective and preventive actions (CAPA).
• Train, mentor, and appraise quality staff to build a high-performing quality culture.
• Lead continuous improvement initiatives to enhance product quality and operational efficiency.
• Prepare and present quality performance reports to senior management and regulatory bodies.

Qualifications & Experience

• Bachelor’s degree in pharmacy, Chemistry, Biochemistry, Microbiology, or related field.
• A master’s degree in quality management, Industrial Pharmacy, or related discipline is an added advantage.
• Minimum of 8–10 years of experience in a GMP-regulated pharmaceutical or biopharmaceutical environment.
• Proven experience in supervisory or managerial roles within Quality Assurance or Quality Control.
• Strong understanding of GMP, GLP, GDP, and ISO quality standards.

How to Apply

All interested candidates who meet the required qualifications and experience are invited to submit their CVs, Cover Letter & Academic documents (addressed to the Head Human Capital).

Application guidelines:

• Merge documents as one PDF or .DOC/.DOCX (max 10MB).
• Email to recruitment@deibiopharma.com with the JOB TITLE IN THE SUBJECT LINE.
• Deadline: 31st October 2025.

Note: Only shortlisted candidates will be contacted within 14 days after the deadline.

Equal Opportunity Employer

Dei BioPharma Ltd. provides equal opportunity and fair and equitable treatment in employment to all people without regard to race, color, religion, sex, national origin, age, disability, political affiliation, marital status, or sexual orientation.

Brown Alex Sunday, 26 October 2025 Health Jobs