Regulatory Affairs Associate jobs in Centurion

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A leading global healthcare company in Midrand is seeking a Regulatory Affairs professional to manage Marketing Authorization applications and maintain product compliance. The ideal candidate will have a BPharm or equivalent, experience in regulatory environments, and strong communication skills. This role emphasizes timely submissions and compliance with local regulations in a hybrid work...

Introduction Our client has a track record of nearly 3 decades in the medical industry! They are a leading South African based distributor of high-quality medical consumables and equipment, working with professionals in both private practice and state health facilities. They are looking for their next superstar Regulatory Responsible Pharmacist! Duties & Responsibilities As their new...

Overview Growing What Matters Starts With You Corteva Agriscience™, the world's first dedicated agriculture start-up, serves to enrich the lives of those who produce and those who consume, ensuring progress for generations to come. Our employees fulfill this purpose everyday by building/participating in an inclusive culture where we encourage each other to stay curious, think differently, act...

Hybrid## Regulatory Program Manager: Seeds & BiotechCenturion, Gauteng, South AfricaJob LocationCenturion, Gauteng, South AfricaYour Responsibilities And Related Challenges Manage seeds and biotech dossiers developments and approval processes in line with business needs and set timelines Support AME Regulatory lead with business strategy developments inputs and support strategy execution Keep...

A leading pharmaceutical company is seeking a Regulatory Affairs professional in Midrand, Gauteng. This role focuses on supporting the submission and approval processes for regulatory dossiers. The ideal candidate will have a strong background in regulatory affairs, data analysis, and stakeholder management. Responsibilities include ensuring compliance with regulations, preparing submissions, and...

Regulatory Affairs Systems & Data Analyst Posting Date: Jan 21, 2026 Country: South Africa State: Gauteng Job Purpose To support the Regulatory Affairs (RA), Medical Affairs (MA), Pharmacovigilance (PV) department by managing and optimizing digital systems, data workflows, and process automation. This role combines regulatory knowledge with strong IT capabilities to ensure accurate data...

Gen-Eye (Pty) Ltd is seeking a Regulatory Affairs Specialist to join our dynamic team. This role is critical in managing regulatory submissions and lifecycle activities for pharmaceutical products, ensuring timely and compliant registration with SAHPRA and other authorities. Location: Midrand, Gauteng, South Africa What You’ll Do - Initiate and manage timely registration processes for new...

Department: Research & Development Location: Roodeplaat, Pretoria Reports to: R&D Manager Classification: Permanent About the Opportunity Our client is a leading South African biotechnology company specialising in the development and manufacture of veterinary vaccines, both registered and autogenous, for poultry, ruminants, and other species. Their work contributes significantly to animal...

A leading chemical distribution company in South Africa is seeking an experienced Regulatory Officer to ensure compliance within the agricultural sector. The ideal candidate will generate regulatory documents, manage compliance records, and liaise with various departments. Candidates must have a tertiary qualification in Agriculture, a Crop Life/BASOS certificate, and 1-2 years of relevant...

QA/RA Pharmacist A pharmaceutical company and applicant for several private label brands is currently seeking an innovative QA/RA pharmacist, passionate about complementary medicines, and will be based in Midrand. The candidate will be responsible for product compliance and involved in new product development. Duties & Responsibilities - Release of imported and locally manufactured...

Adcock Ingram Holdings Limited and its Subsidiaries ("we", "us") is committed to protecting and respecting your privacy. Our Privacy Notice sets out the basis on which personal information collected inter alia from you, social media, recruitment agencies and our website, will be processed by us. The Privacy notice is available on our website One of the conditions under the Protection of Personal...

A leading pharmaceutical company in Midrand seeks a Regulatory Affairs specialist to support pre-registration and post-registration dossier submissions. You will ensure timely communication and compliance with the SAHPRA. The ideal candidate has a degree in Pharmacy or Regulatory Affairs with strong experience in dossier management and stakeholder engagement. This role is crucial to support new...

Job Purpose Support the Regulatory Affairs function in its pre‑registration and/or post‑registration dossier submission activities by assisting in data gathering, screening, collating and compiling of the dossiers, post‑registration variations and any other documentation in order to submit the same to the Health Authorities for approval within the defined timelines as per overall objective of...

Job Description Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory agencies. We are on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Position Overview -...

A leading biotechnology company in Pretoria seeks a Regulatory Affairs Pharmacist to ensure compliance and oversee the lifecycle management of veterinary vaccines. The ideal candidate will have experience in regulatory affairs, strong technical writing skills, and be registered with SAPC. This position involves engaging with regulatory authorities and compiling necessary submissions to maintain...

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Support the Regulatory Affairs function in its pre-registration and/or post-registration dossier submission activities by assisting in data gathering, screening, collating and compiling of the dossiers, post-registration variations and any other documentation in order to submit the same to the Health Authorities for approval within the defined timelines as per overall objective of Cipla...

The objective of the programme is to provide a qualified graduate with meaningful workplace experience in Regulatory Affairs. Required Learning - B Pharm degree - Completed Community Service - Industry knowledge will serve as added advantage - NSFAS Funded would be advantageous Core Competencies - Intermediate Computer Literate (MS Package) - Good interpersonal skills and...

A leading healthcare company in Midrand is offering an internship in Regulatory Affairs for qualified graduates. Candidates must possess a B Pharm degree and have completed Community Service. The role emphasizes strong interpersonal, communication, and organizational skills, with knowledge of the industry being advantageous. The internship aims to provide meaningful workplace experience,...