Coordinate generation, resolution and submission of CAPA and follow up on external audits
Participate in new products development
Responsible for all regulatory requirement of the factory premises and products in accordance with all pharmaceutical regulations in Nigeria and Industry standards.
Monitoring of CGMP compliance company-wide.
Maintaining all relevant registers and records.
Training and sensitization of staff on new regulations and guidelines
Preparation and review of training manual.
Coordination with the supportive depts., to achieve the production targets.
Monitoring dispensing operations.
Facilitate application for necessary export permits and requirements
Liaise and represent the company all the regulatory bodies such as PCN, NAFDAC, PMG MAN, national and state ministry of Trade and industry, ministry of labor, ministry of environment and ministry of health and safety and others that have bearing on company activities
Register and renew the Factory license annually.
Register and renew the Pharmacist license annually.
Register new products and renew products licenses accordingly.
Monitor and control usage and distribution of controlled substances.
Apply for import permit of chemicals, controlled substance, and active pharmaceutical ingredient.
Follow up environmental monitoring.
Facilitate and participate in production/quality management
Responsible for all registrations with corporate bodies, source for the necessary information, get the appropriate documents for Registration
Bachelor of Pharmacy (B. Pharm).
Valid license to practice as a Pharmacist.
(5) years of production work experience in the pharmaceutical industry.
Functional knowledge of production lines and production operations is an advantage.
Must be computer literate and familiar with Ms Office applications
Proven experience in training and development of staff to meet set goals.
Excellent communication skills (verbal and written).
Ability to multi-task, and change priorities constantly as needed in a fast-paced environment.
Possesses basic knowledge of drug manufacturing and GMP.
Experience with product registration