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|The Superintendent Pharmacist by Pearlcon: 12:46pm On Dec 08, 2017|
a. Responsible for regulatory affairs.
b. Liaising with external bodies and agencies on healthcare and medical matters.
c. Responsible for organizing product licenses; Responsible for authorization of production, Batch Manufacturing Record (BMRs) and document review
d. Responsible for supervising Quality Management System (QMS); Ensures Good Manufacturing Practise (GMP) is adhered
e. Co-ordination of clinical presentations and meetings with Private Sector clinics, Federal and State Government Health institutions
f. Co-ordination of imports of finished formulations and APIs
g. Liaising with bodies such as the Pharmaceutical Group of the Manufacturers Association of Nigeria (PMGMAN), National Agency for Food Drugs Administration and Control (NAFDAC), Pharmacists Council of Nigeria (PCN), Pharmaceutical Society of Nigeria (PSN), Federal and State Ministries of Health, Customs and Excise Authorities
h. Interface with multilateral and Development Agencies such as World Health Organization (WHO), West African Health Organization (WAHO), United Nation Industrial Development Organization (UNIDO), Economic Community of West African States (ECOWAS), International Finance Corporation (IFC) & Centre for Development Enterprise (CDE) on Healthcare and Medicinal matters
i. Conduct training to Pharmacists on QMS, CGMP and job-related aspects
j. Attends to any incidental work that may be required by the Factory Manager
k. Registration of premises with the Pharmacists Council of Nigeria (PCN); Registration of products with the National Agency for Food Drugs Administration and Control (NAFDAC).
l. Clinically screen prescriptions to ensure safe, optimal and cost-effective use of the medicine.
m. Take overall responsibility for setting out the standards and policies for the provision of professional pharmacy service
n. Handle record keeping mechanisms and standard operating procedures
a) Bachelor's Degree in Pharmacy
b) Minimum of 5 years’ experience in Pharmaceuticals manufacturing as Superintendent Pharmacist
c) Knowledge of Drug Rules and manufacturing of Pharmaceutical Dosage Forms.
d) He/she must have a working relationship & or dealing with NAFDAC especially in the areas of product registration and importation
e) Compliance with GMP
f) The individual must have a working knowledge of product registration and import and export control requirements with regular agencies.
g) Leadership skills; Time Management; Team Spirit; Interpersonal skills; Attention to details
To apply, send you CV to firstname.lastname@example.org or email@example.com with subject name.
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