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Salary
≈ $8k – $20k per year (Estimated)
Location
In office (Nairobi)
Employment
Full-Time

First seen by Alion on Oct 23, 2026.

Overview
Company
Impact
Profile match
MSVL Group is a recruitment, HR consulting and corporate training firm serving employers across Africa, India and the Middle East. With over 10 years of experience, it hires for client roles such as pharmaceutical quality managers, hotel key account managers, production supervisors and teachers. The company is headquartered in Nairobi, Kenya.

MSVL Group is a leading provider of recruitment, HR consulting, and corporate training services, with over 10 years of experience across Africa, India, and the Middle East. We specialize in sourcing top talent, from entry-level to executive roles, and offering tailored HR solutions that align with our clients’ business goals. Our expertise spans multiple i...
Quality Control Manager (Pharma)


Qualifications, Skills and Experience

Bachelor's degree in Chemistry, Pharmacy, Pharmaceutical Sciences, Microbiology, Laboratory Technology, or a related scientific field.
Minimum 7 years of QA/QC experience in pharmaceutical manufacturing, including at least 5 years in a managerial role.
Strong experience in pharmaceutical QC testing, analytical methods, laboratory operations, and quality management systems.
In-depth knowledge of cGMP, GLP, regulatory compliance, SOPS, and pharmaceutical quality standards.
Experience in method validation, stability studies, equipment qualification, audits, and quality investigations.
Strong understanding of QC laboratory instruments, analytical equipment, and quality documentation systems.
Proven leadership, analytical, problem-solving, organizational, and communication skills.
Proficiency in Microsoft Office and laboratory reporting systems.

Key Responsibilities

Oversee QC laboratory operations, ensuring timely testing of raw materials, packaging materials, intermediates, and finished products.
Develop and maintain QC standards, specifications, SOPs, testing procedures, and quality documentation.
Ensure compliance with cGMP, GLP, regulatory requirements, and data integrity standards.
Manage analytical method validation, stability testing, equipment calibration, qualification, and laboratory maintenance.
Review batch records, analytical results, and approve or reject materials and products based on QC findings.
Lead investigations into deviations, out-of-specification results, customer complaints, and corrective actions.
Coordinate internal and external audits, regulatory inspections, quality risk management, and continuous improvement initiatives.
Manage departmental budgets, laboratory resources, performance targets, and QC team training and development.

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