• Head of Regulatory Affairs and Responsible Pharmac South Africa
  • MNA Recruitment in South Africa, , South Africa
  • jobs
  • 1 week ago

jobs description

Reference: DBN003556-SS-1

A global pharmaceutical company has a vacancy for a Head of Regulatory Affairs and Responsible Pharmacist.

Duties & Responsibilities

Job Purpose:
• To describe the role and responsibilities of the Responsible Pharmacist as contemplated in regulation 25 (3) of the Pharmacy Act and the relevant sections of the Medicines Act (Act 101 of 1965) and the South African Guide to Good Manufacturing Practices

Main Duties and Responsibilities are:
• Responsible Pharmacist Duties as per latest applicable legislation:
• Responsible for the continuous supervision of the actions and activities of the pharmacy to ensure on-going compliance to relevant Acts, Regulations, Guidelines and Codes.
• Responsible to ensure that pharmacists who provide services forming part of the scope of pharmacy practice are appropriately registered with the Pharmacy Council.
• Responsible to ensure that defined roles and responsibilities for personnel exists and that training programs are... implemented and maintained, that personnel are trained in cGMP and that continuous training is in place.
• Responsible to ensure the company is in possession of the required License/s from SAHPRA to conduct its business.
• Responsible for the registration of medicines with the South African Health Products Regulatory Authority and the maintenance of these registrations.
• Responsible and accountable to the South African Health Products Regulatory Authority and the South African Pharmacy Council for compliance with the provisions of the Medicines and Related Substances Act, 1965 (Act 101 of 1965) and its Amendments relating to the sale, control of the manufacturing and distribution of medicines, scheduled substances, or medical devices.
• Responsible for notifying the SA Pharmacy Council immediately upon receiving knowledge that his/her services as Responsible Pharmacist have been or will be terminated.
• Responsible for taking corrective measures in respect of deficiencies regarding inspection reports of the SAPC or SAHPRA.
• Responsible to ensure that a Pharmaceutical Quality Management System is in place.
• Responsible for initiating and coordinating all recall activities, in collaboration with the head of Quality Management.
• Responsible to ensure that a letter of authorization to communicate with SAHPRA, signed by the CEO, is submitted to SAHPRA.
• Responsible for the compilation of a letter of delegation of authority in his/her absence.
• Responsible for compliance with Good Pharmacy Practice as published by the SA Pharmacy Council.
• Responsible for participating in decision-making processes affecting the pharmacy business.
• Responsible to supervise every pharmacist appointed by the company.
• Responsible for compliance by the pharmacy owner with all the conditions of ownership of the pharmacy business and registration of the pharmacy.
• Responsible to ensure that no person is appointed to perform any act falling outside the scope of practice of the category in which such person is registered or which he/ she is not authorized to perform in terms of the Pharmacy Act, 1974 (Act 53 of 1974).
• Responsible to report in writing, any non-compliance with the Pharmacy Act to the management of such pharmacy business and to furnish the SA Pharmacy Council with a copy thereof.
• Responsible to ensure that no instruction or order of management with regard to the pharmacy business that could amount to a contravention of legislation applicable to the pharmacy business, is introduced or carried out.
• Accountable for the release for sale of finished product.
• Ensures the completion of all individual assigned training within the specified timelines.
• Forwarding of all received Product Quality Complaints, Adverse Events and Medical Enquiries to the relevant person in Quality Assurance/ Pharmacovigilance/ Medical Affairs.
• Ensure the availability of training plans according to the direct report’ s role profiles within the team
• Ensure that he relevant training has been completed according to the training plan.

Head of Regulatory Affairs Duties:
• Ensuring alignment of global and regional commercial strategic plan with the Regulatory affairs submission plans for all markets within the region.
• Lead and manage the regional team in developing regulatory strategies for registering new products and line extensions and their life cycle management.
• Develop strong partnerships within the country and cross regional teams to facilitate development and implementation strategies.
• Preparation of the Africa RA budget and tracking actual vs projected spend.
• Identification of key RA compliance projects and facilitating the implementation thereof.
• Mentorship of the Senior RA Managers with the intention of succession planning.
• Form part of the regional executive committee team and provide insight into RA activities and report on department progress.
• Form part of the global Senior Leadership team and ensure alignment between global and regional strategies.
• Conduct ongoing risk assessments and development of strategies to mitigate associated risk.
• Conducting regulatory intelligence activities and determine the impact of applicable intelligence on the company

Qualifying Requirements are:
• Must be a qualified Pharmacist (Bachelor of Pharmacy Degree and/or equivalent) with a valid registration with the SA Pharmacy Council.
• Should have a maximum of 10 years of senior management experience within the pharmaceutical environment.
• Have must sound knowledge of the principles of GxP requirements and SAHPRA guidelines across Orthodox medicines, cosmetics, complimentary medicines and medical devices.
• Embodies Values & Behaviours in all internal and external interactions.
• Excellent written and verbal communication skills.
• Ability to lead large strategic projects
• People skills – highly adapted interpersonal skills.
• Problem solving analysis skills.
• Priority setting – initiative and follow through.
• Time management and deadline driven.
• Ability to analyse complex data, seek relevant opinions.
• Detail oriented, organized and structured.
• Agile and easily adaptable.

Candidates that meet the criteria may submit their applications via this portal or via vacancy link on www.mnarecruitment.com
Should you receive no feedback within 7 days, please accept your application as unsuccessful
South Africa


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