Superintendent Pharmacist at Oak-Faith Pharmaceutical Resources Limited

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.