SH
Executive – Quality Control at Shalina Healthcare
RÉCENTCDI3 days ago
Job Description
Ogun
CDI
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Executive – Quality Assurance
Shalina Healthcare, one of the largest pharmaceutical companies in sub-Saharan Africa, is recruiting for the position of Executive – Quality Assurance. For the past 35 years, we have been dedicated to providing quality medicines to those who need them most. We manufacture and distribute branded prescription and over-the-counter pharmaceutical and consumer products across various therapeutic groups, including anti-malarial, antibiotics, anti-inflammatory, and nutrition. Our track record is unmatched, and our brands are among the most trusted in Africa.
Location: Ogun, Nigeria
Employment Type: Full-Time
Department: Quality Control
Job Description: To ensure that all pharmaceutical products are manufactured, tested, and released in compliance with regulatory standards, company policies, and Good Manufacturing Practices (GMP), thereby guaranteeing product quality, safety, and efficacy.
Key Responsibilities:
Quality Compliance & GMP: Ensure adherence to Good Manufacturing Practices (GMP), SOPs, and regulatory guidelines (e.g., NAFDAC, WHO, FDA where applicable). Monitor manufacturing and packaging processes to ensure compliance with approved procedures. Participate in internal and external audits and regulatory inspections.
Documentation & Record Control: Review batch manufacturing records (BMR), batch packaging records (BPR), and other quality documents for accuracy and completeness. Ensure proper documentation practices (GDP) are followed across all departments. Maintain and control SOPs, specifications, and quality records.
In-Process Quality Assurance: Perform line clearance before and after production activities. Conduct in-process checks and ensure compliance with quality standards during manufacturing. Monitor environmental conditions where required.
Qualifications & Requirements:
Bachelor’s Degree (B.Sc./HND) in Pharmacy, Microbiology, Biochemistry, Chemistry, or any related science discipline. Professional certification or membership (e.g. NIPR, or relevant regulatory body) is an added advantage. 5–8 years’ experience in a pharmaceutical manufacturing company. Strong knowledge of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and regulatory requirements (NAFDAC, WHO guidelines). Experience in documentation review, deviation handling, CAPA, and audit processes. Proficiency in Microsoft Office applications (Excel, Word, PowerPoint). Good understanding of quality systems, risk management, and validation processes.
Application Closing Date: Not Specified.
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Your safety comes first — read before you go
Taf4All only lists job offers published by third parties. We are not the employer, we do not conduct these recruitments, and we cannot guarantee what happens once you make contact — you deal directly with the person or company behind the offer, at your own risk.
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