Associate Manager - Quality Control

Shalina Healthcare | Ogun, Nigeria

Full-Time Posted today 0 views

About the Role

Shalina Healthcare is a market leader dedicated to making quality healthcare products affordable and accessible across Africa. We are currently seeking a dynamic and experienced Associate Manager - Quality Control to join our growing team in Nigeria. In this critical leadership role, you will oversee all quality control activities within our manufacturing facility, ensuring that raw materials, in-process products, and finished goods consistently meet the highest quality standards, internal policies, and stringent regulatory requirements.

Key Responsibilities
  • Manage and supervise all Quality Control laboratory operations, including chemical, microbiological, and instrumental analysis.
  • Ensure rigorous testing of raw materials, packaging materials, in-process samples, and finished products against approved specifications.
  • Review and approve laboratory results, certificates of analysis (CoA), and comprehensive test reports.
  • Maintain strict compliance with regulatory requirements such as GMP, GLP, WHO, and NAFDAC guidelines.
  • Oversee the calibration, qualification, and routine maintenance of advanced laboratory equipment.
  • Lead investigations regarding Out-of-Specification (OOS), Out-of-Trend (OOT), and operational deviations, ensuring proper documentation and timely closure.
  • Develop, review, and update Standard Operating Procedures (SOPs), specifications, and analytical test methods.
  • Coordinate stability studies and ensure accurate documentation and reporting.
  • Manage, mentor, and train QC staff, conducting regular performance evaluations.
  • Support internal and external audits, including official regulatory inspections.
  • Collaborate cross-functionally with Production and Quality Assurance to safeguard product quality and compliance.
Qualifications
  • Bachelor Degree in Pharmacy, Chemistry, Biochemistry, Microbiology, or a related field (Master Degree is an added advantage).
  • 10 to 15 years of proven experience in pharmaceutical manufacturing, with at least 3 to 5 years in a managerial or supervisory role.
  • Strong, demonstrable knowledge of GMP, GLP, and regulatory frameworks such as NAFDAC and WHO.
  • Hands-on experience operating analytical instruments including HPLC, GC, and UV Spectrophotometers.
  • Exceptional leadership, organizational, problem-solving, and communication skills.
  • High attention to detail, commitment to data integrity, and strong report-writing capabilities.
Benefits
  • Competitive salary package commensurate with experience and industry standards.
  • Opportunities for professional growth and career advancement within a leading multinational healthcare company.
  • Comprehensive health insurance and wellness benefits.
  • A collaborative, inclusive work culture that values employee contribution to community health.

Skills

Quality Control GMP GLP NAFDAC Compliance Laboratory Management HPLC Pharmaceutical Manufacturing People Leadership
Report this job listing