U
Pharmacist
Unknown · Ogun
Salary
Undisclosed
Location
Ogun
Posted
7 hours ago
Required skills
GMP complianceQuality assuranceQuality controlRegulatory complianceDocumentation and record managementPharmaceutical manufacturingRisk assessmentProblem-solvingAttention to detailMicrosoft OfficeCommunicationTeamwork
About the role
Pharmacist
Support the development, manufacturing, quality assurance, regulatory compliance, and distribution of pharmaceutical products in a production environment. Ensure all products meet GMP standards, regulatory requirements, and company quality policies while promoting patient safety and product effectiveness.
Responsibilities
- Ensure compliance with GMP, GDP, and applicable pharmaceutical regulations
- Supervise and monitor manufacturing processes to meet quality standards
- Review and approve batch manufacturing and packaging records
- Conduct quality assurance and quality control activities, including reviewing test results and investigating deviations
- Monitor product stability and proper storage and handling of pharmaceutical products
- Prepare and maintain accurate regulatory documentation
- Participate in internal and external audits and implement corrective and preventive actions (CAPA)
- Support product registration, licensing, and regulatory submissions
- Investigate customer complaints, product defects, and recalls
- Provide technical guidance and training to production and quality personnel
- Collaborate with R&D, production, engineering, and regulatory teams
- Ensure compliance with health, safety, and environmental policies
- Stay updated with pharmaceutical regulation changes and industry best practices
Requirements
- Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D.)
- Valid pharmacist license/registration with appropriate regulatory authority
- Knowledge of GMP, GDP, GLP, and pharmaceutical quality systems
- Strong analytical and problem-solving skills
- Excellent communication and teamwork abilities
- Proficiency in Microsoft Office and pharmaceutical documentation systems
- Experience in pharmaceutical manufacturing, quality assurance, quality control, or regulatory affairs (preferred)
How to Apply
Interested and qualified candidates should send their CVs to: nosa@svnl.in using the job title as the subject of the email.
Application Closing Date: 31st July, 2026
📋 How to apply
Follow the application instructions in the How to Apply section of the role description above (email, phone, or link as posted by the employer).