Lead Quality Control Operations in Nigeria’s Pharmaceutical Manufacturing Industry

Biomedical Limited is inviting applications from experienced quality assurance professionals for the position of Quality Control Manager / Head, Quality Control at its manufacturing facility in Ilorin, Kwara State.

The company is seeking a seasoned professional with extensive experience in pharmaceutical quality control, regulatory compliance, and laboratory leadership to oversee quality management processes and maintain high manufacturing standards.

About Biomedical Limited

Biomedical Limited is one of Nigeria’s pioneering pharmaceutical manufacturers. Established in 1978, the company became the first pharmaceutical manufacturer in Nigeria to produce intravenous fluids, dialysis solutions, irrigation fluids, and oral rehydration salts locally.

Operating from its production facility in Ilorin, Biomedical Limited has played an important role in strengthening Nigeria’s healthcare sector through the manufacture of critical life-saving medical products while maintaining a strong commitment to product quality and regulatory compliance.

Position Overview

The Quality Control Manager will provide strategic and operational leadership for the company’s quality control department. The successful candidate will oversee laboratory quality activities, ensure compliance with pharmaceutical regulations, and support continuous improvement across manufacturing processes.

This position requires strong technical expertise, leadership ability, and extensive knowledge of pharmaceutical quality systems.

Key Responsibilities

The successful candidate will be expected to:

• Lead and supervise the Quality Control department.
• Ensure compliance with NAFDAC regulations and pharmaceutical quality standards.
• Oversee laboratory testing and quality control processes.
• Support continuous improvement initiatives across quality management systems.
• Apply advanced quality control tools and technologies to improve operational performance.
• Provide leadership to quality control personnel and support staff.
• Analyze quality data and recommend corrective or preventive actions where necessary.
• Contribute to maintaining product safety, consistency, and regulatory compliance.

Qualifications

Applicants should possess:

• A Bachelor’s Degree in one of the following disciplines:
  • Chemistry
  • Industrial Chemistry
  • Biochemistry
  • Pure and Applied Chemistry
  • Or another closely related scientific field
• A minimum academic qualification of Second Class Upper Division (2:1).

Experience Required

Candidates should have:

• At least 15 years of professional experience in quality control within the pharmaceutical or related manufacturing industry.
• Proven leadership or management experience.
• Strong understanding of NAFDAC regulations and pharmaceutical compliance requirements.
• Experience using modern quality control software and laboratory systems.

Skills and Competencies

The ideal candidate should demonstrate:

• Strong analytical and critical thinking skills.
• Excellent problem-solving ability.
• Project management experience.
• Leadership and team management capabilities.
• Good communication and decision-making skills.
• Commitment to maintaining high quality and regulatory standards.

Who Should Apply?

This opportunity is suitable for senior pharmaceutical quality professionals, laboratory managers, quality assurance leaders, and experienced scientists seeking a leadership role within a well-established pharmaceutical manufacturing company.

Applicants with extensive regulatory compliance experience and a proven track record of managing quality control operations are encouraged to apply.

Tips Before Applying

To strengthen your application:

• Highlight your pharmaceutical quality control experience.
• Clearly demonstrate your leadership and supervisory responsibilities.
• Include your experience with NAFDAC compliance and quality management systems.
• Mention any laboratory management, audit, or regulatory inspection experience.
• Ensure your CV reflects your most recent technical and managerial achievements.

How to Apply

Interested and qualified candidates should send their updated CV to any of the following email addresses:
solaotitolaye@yahoo.com, recruitment@biomedicalng.com, sola.otitolaye@biomedicalng.com

Use “Quality Control Manager / Head, Quality Control” as the subject line of your email.

Applications should be submitted on or before 15 July 2026.

Final Thoughts

Quality control leadership plays a vital role in ensuring the safety and effectiveness of pharmaceutical products. This position offers experienced professionals an opportunity to contribute to a long-established Nigerian pharmaceutical manufacturer with a strong history of producing essential healthcare products.

Before submitting your application, review the requirements carefully and ensure your CV highlights your leadership experience, regulatory knowledge, and technical expertise in pharmaceutical quality control.