Location: Ibadan, Oyo Responsibilities The suitable candidate will be responsible in the following aspect:
Responsible for regulatory affairs.
Assist in liaising with external bodies and agencies on healthcare and medical matters.
Responsible for authorization of production, Batch Manufacturing Record (BMRs) and document review.
Ensures Good Manufacturing Practice (GMP) is adhered
Ensure customer complaints are resolved
Liaison with Government and Statutory Agencies and Medical Institutions.
Attends to any incidental work that may be required by the Factory Manager
Assist in registration of premises with the pharmacists 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
Requirements
Bachelor’s Degree in Pharmacy
Minimum of 2-3 years experience in Pharmaceuticals manufacturing.
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.
Must be based in Ibadan
He / she must have a working relationship & or dealing with NAFDAC especially in the areas of product registration and importation
Compliance with GMP
Applicants should send their CV’s to: jobs@lorachegroup.com
Apply via :
jobs@lorachegroup.com
