Oak-Faith Pharmaceutical Resources Limited is a Limited Liability Company (LLC ) with RC number 272095. Utilizing over 20 years of experience and success in the pharmaceutical industry, Oak-Faith Pharma has created. We are a Limited Liability Company (LLC) with RC number 272095. Utilizing over 20 years of experience and success in the pharmaceutical industry, Oak-Faith Pharma has created.
We are recruiting to fill the position below:
Job Title: Superintendent Pharmacist
Location: Mowe, Ogun
Employment Type: Full-time
Reporting to: Managing Director
Job Purpose
To coordinate and document internal regulatory processes, such as Internal Audits, Inspections, license renewals, or registrations. Compile and prepare materials for submission to regulatory agencies, NAPAMS, PMG – MAN
Principal Accountabilities
Responsible for:
Production Planning and Inventory control
Product formulation development
Responsible for:
Research foreign market for brand entrance / introduction
Generating as often as required articles on general health topics, and content on health, diseases, upload on websites & other marketing needs.
Responsible for the company’s advertisement, Post Marketing surveillance.
Registration & renewal of premises, annual Pharmacists’ license by liaising with the Regulatory Authority, Pharmacists Council of Nigeria (PCN)
Registering and processing the licenses for the Pharmacists in the organization.
Liaising with regulatory agencies regarding pre-submission guidelines, compliance directives, clarification, follow-up of submissions.
Facilitating businesses within the Pharmaceutical Industry in Nigeria
Co-ordination of tenders for supplies to health institutions.
Co-ordination of Clinical Presentations and meetings with Private Sector clinics, Federal and State Government Health Institutions as necessary.
Co-ordinate the writing of Common Technical Documents (CTD) dossiers, applications on E-trade portal, Contract Manufacturing procedures and processes.
Co-ordinate applications on NAPMANS (New Registrations, Renewals, Valuation, Data capture)
Co-ordinate the Quality Management Review meetings according to schedule.
Co-ordinate, Planning and self-inspections / self audit to ensure compliance with CGMP and regulatory requirements.
Planning and undertaking regulatory inspections.
Co-ordinate the Pharmaco-vigilance program of the organization.
Offer technical assistance for products research and development.
Be involved in Products Research & Development process.
Effective handling of cGMP & Training, CAPA Management
Co-ordinate Medical and Laboratory tests for employees.
Be involved in QA Department review of their SOPs
Ensure final endorsement & authorization of all SOPs for Production, Quality Assurance and Regulatory documents.
Partake in Annual Product Quality Review and Data Analysis
Responsible for the Registration & Renewal of products, liaising with the Regulatory Authorities: National Agency for Food Drugs Administration and Control (NAFDAC) & PCN.
Managing other duties that may be assigned by the Managing Director.
Background Experience / Qualifications
Minimum Education: A good Bachelor's Degree / HND in Sciences (Chemistry, Biochemistry, Biology, Pharmacy)
Formal Training / Professional / Professional Certifications: Conferences, courses and Seminars/ Professional membership is an added advantage
Minimum Relevant Experience: 5 years post qualification experience.
Required Age: 30 & above.
Personal Specification:
Excellent listening skills
Logical and proactive
Strong analytical skills
Attention to details
Computer literate with data analysis skills
Great adaptability to work, and easy learning of new skills
Good organizational skills developed in a variety of deadline-orientated situations.
Good working relationships at all levels.
Good presentation and communication skills (written and clear verbal communication).
Application Closing Date
30th November, 2021.
How to Apply
Interested and qualified candidates should send their CV to: [email protected] using the Job Title as the subject of the mail.