Quality Assurance Executive at Shalina Healthcare

• 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.

• 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.

• 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.
• Minimum of 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.