Posted on: Tue 17-12-2019

• Responsible for regulatory affairs.
• Liaising with external bodies and agencies on healthcare and medical matters.
• Responsible for organizing product licenses
• Responsible for authorization of production, Batch Manufacturing Record (BMRs) and document review
• Responsible for supervising Quality Management System (QMS)
• Ensures Good Manufacturing Practice (GMP) is adhered
• Ensure customer complaints are resolved
• Liaison with Government and Statutory Agencies and Medical Institutions
• Conduct training to Pharmacists on QMS, CGMP and Job-related aspects
• Attends to any incidental work that may be required by the Factory Manager
• Registration of premises with the pharmacist’s council of Nigeria (PCN).
• Registration of products with the National Agency for Food Drugs. Administration and Control (NAFDAC).
• Maintain standards at NOSDOC GROUP,
• Clinically screen prescriptions to ensure safe, optimal and cost-effective use of the medicine.
• Take overall responsibility for setting out the standards and policies for the provision of professional pharmacy service
• Handle record keeping mechanisms and standard operating procedures.

• Bachelor's Degree in Pharmacy
• Minimum of 5 years’ experience in Pharmaceuticals manufacturing as Superintendent Pharmacist
• Knowledge of Drug Rules and manufacturing of Pharmaceutical Dosage Forms.
• The individual must have a working knowledge of product registration and import and export control requirements with regular agencies.
• The possession of a working relationship & or dealing with NAFDAC especially in the areas of product registration and importation is desired but not compulsory.
• Compliance with GMP.

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