Regulatory Manager jobs in Midrand

Company Description At Deloitte, our Purpose is to make an impact that matters for our clients, our people, and society. We harness the talent of 450,000+ people located across more than 150 countries and territories to deliver lasting impact through our global strategy, services, and collaborations. Job Description About Regulatory Risk We are reshaping regulatory trends using cutting-edge...

Reference: PTA000135-SM-1 As a Regulatory Certification Manager in the automotive industry, your primary responsibility is to ensure that vehicles and automotive products comply with local, national, and international regulations and standards. You will oversee the certification process from start to finish, working closely with regulatory agencies, internal teams, and external partners to...

Hire Resolve's client is actively seeking a Regulatory Affairs Manager to join their team in Midrand, Gauteng. As a Regulatory Affairs Manager, you will be responsible for ensuring a thorough and seamless product registration process and dossier maintenance. You will ensure that the company complies with all regulations and maintains pharmacovigilance requirements. Responsibilities - Lead,...

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...

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...

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...

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...

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 www.adcock.co.za. One of the conditions under the...

A leading pharmaceutical company in Midrand seeks a candidate for a Regulatory Affairs role. The individual will provide system, administrative, and technical support across regulatory systems, ensuring compliance and data integrity. Candidates should possess a BSc degree in Life Sciences or a related field and have 2-4 years of relevant experience. Strong interpersonal and organizational skills...

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 professional services firm is seeking an experienced regulatory compliance manager to lead client projects and drive legal strategy. The ideal candidate will have extensive experience in regulatory and compliance risk management, alongside strong project management skills. Responsibilities include advising clients, drafting legal agreements, and implementing compliance solutions....

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...

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 pharmaceutical company based in Midrand is looking for a Regulatory Affairs Systems & Data Analyst. In this role, you will support the Regulatory Affairs and Medical Affairs by managing data workflows and optimizing digital systems. The successful candidate will need a diploma in IT or Computer Science, alongside 1-2 years of experience in data analytics. Key responsibilities include...

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...

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...