• Essential: Relevant Bachelor’s degree (e.g. Pharmacy, Health Sciences, Regulatory Affairs). 

• Advantageous: Additional qualifications in Quality Assurance, Regulatory Compliance, or Manufacturing Sciences. 

• Experience: Minimum 5 years in regulatory affairs or NPD, with exposure to pharmaceutical, medical device, complementary, nutritional, and V- or G-registrations. 

• Demonstrated experience with dossier development, submissions, and regulatory approvals. 

• Strong working knowledge of SAHPRA, Act 36, GMP, and international registration processes. 

• Proven background in QMS development and pharmaceutical manufacturing compliance. 

 
Key Responsibilities 
Regulatory Affairs 

• Lead the preparation, submission, and follow-up of new product registrations and renewals. 

• Conduct dossier gap analyses, recommend corrective actions, and ensure timely approvals. 

• Build and maintain a centralised database of product registrations, legal documents, and timelines. 

• Act as the primary liaison with regulatory authorities and external stakeholders. 

Quality Management Systems (QMS) 

• Design, implement, and maintain SOPs, quality manuals, and QMS integrations. 

• Oversee site compliance activities including updates to the Site Master File. 

• Monitor adherence to GMP standards and drive continuous quality improvement. 

New Product Development (NPD) 

• Provide regulatory expertise during product design, formulation, and label development. 

• Ensure new products meet both regulatory and commercial requirements. 

• Collaborate with marketing, manufacturing, and legal teams to align innovation pipelines. 

• Draft and review product inserts, labels, and information leaflets. 

Manufacturing & Validation 

• Approve manufacturing processes, equipment validations, and supplier quality checks. 

• Oversee batch release procedures, ensuring all testing and documentation are in order. 

• Sign off manufacturing specifications and ensure regulatory alignment. 

Exports & International Registration 

• Manage submissions for SADC and international markets, ensuring compliance with foreign regulations. 

• Maintain strong networks with global registration bodies to support expansion strategies. 

 
Skills & Competencies 

• Strong sense of urgency and results orientation. 

• High attention to detail, with excellent planning and organisational ability. 

• Independent decision-maker with strong collaboration skills. 

• Creative problem-solving with resilience under pressure. 

• Ability to simplify complex regulations into actionable business strategies. 

 
Preferred Experience & Knowledge 

• G/V/Complementary product registrations. 

• Regulatory dossier submissions and renewals. 

• Quality systems setup and pharmaceutical manufacturing compliance. 

• Healthcare and nutritional product development. 

 
 
Closing Date: 
Submissions for this vacancy will close on 09 September 2025, however, you will still have the opportunity to submit your CV for this position till 02 October 2025. 
 
Please Note: 
Thank you for submitting your CV to Marvel Placement Consultants. We value your submission, and we try our utmost best to get back to each applicant. However, should your application be successful, we will be in contact with you. Should you not hear from us within two weeks of application, please consider your application as unsuccessful. We are, however, recruitment specialists and will keep your details on our database for possible future opportunities. 
 
PoPI Act: 
Please note that Marvel Placement Consultants adhere to the POPI Act (Act No. 4 of 2013: Protection of Personal Information Act, 2013). Section 9 of PoPI states that “Personal Information may only be processed if, given the purpose for which it is processed, it is adequate, relevant and not excessive”.