The application closing date:29 Sept 2026 Description: The Clinical Trials Unit (CTU) Manager will be responsible for operational oversight, planning, implementation and conduct of assigned clinical trials and in compliance with applicable clinical and regulatory standards
Division Department Sub Department 1 Job Purpose To oversee and manage centralized vendor management activities across multiple Cipla business units and regions. This includes ensuring compliance with Good Manufacturing Practices (GMP) and quality standards for all
Novartis is seeking a Quality Assurance Pharmacist to provide QA/QC expertise, guidance and support to manufacturing and supply activities to ensure compliance with c GMP and company standards. The role involves batch record reviews, Product Quality
Operations Lead The Operations Lead will be based in Midrand and responsible for ensuring optimum utilisation of all laboratory resources, quality, and timely results to customers. The incumbent will be instrumental in securing the technical competency
Operations Lead Reference: JHB -Sines-1 Our client is looking for an Operations Lead who will be responsible for ensuring optimum utilization of all laboratory resources, quality, and timely results to our customers. The individual will be
Operations Lead Reference: JHB -Sines-1 Our client is looking for an Operations Lead who will be responsible for ensuring optimum utilization of all laboratory resources, quality, and timely results to our customers. The individual will be
Operations Lead The Operations Lead will be based in Midrand and responsible to ensure optimum utilisation of all laboratory resources, quality and timeous results to customers. The incumbent will be instrumental in securing the technical competency
Its more than a job As a member of the Freight Forwarding team Kuehne+Nagel, you will play a key role in transporting goods, optimising processes, and fulfilling our customers promises. At Kuehne+Nagel, our contribution counts in
Job Description Summary Provide quality assurance expertise, guidance and support to operational activities to ensure compliance with applicable regulatory requirements and Novartis procedures and quality standards. Job Description Major Accountabilities Batch record review and related activities
Pretoria, South Africa | Posted on 08/18/2026 Industry Pharma/Biotech/Clinical Research Work Experience 4-5 years State/Province Gauteng Country South Africa Job Description The Responsible Pharmacist will oversee the day-to-day operations of the pharmacy and act as the
The primary purpose of this position is to serve as the Responsible Pharmacist (RP) for the company and to exercise the professional, statutory and regulatory accountability required for the licensed manufacturing pharmacy and legal entity in
Glaxo Smith Kline South Africa seeks a seasoned Pharmaceutical Manufacturing Quality Assurance Manager to lead the QA function at the Cape Town site, ensuring GMP/GXP compliance and robust quality systems. You will drive audits, batch release oversight,
Cape Town, South Africa | Posted on 14/05/2026 A leading organisation in the healthcare and manufacturing sector is looking to appoint a dynamic, passionate, confident, proactive, and meticulous Data Analyst to join a goal-oriented team. The
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a CSV Validation Engineer based in South Africa. This is a senior, hands-on validation
Company Overview Glaxo Smith Kline South Africa (GSK) is a leading global healthcare company dedicated to improving the health and well‑being of people worldwide. With a strong presence in Cape Town, GSK operates state‑of‑the‑art manufacturing facilities
The primary purpose of this position is to serve as the Responsible Pharmacist (RP) for Pfizer Laboratories (Pty) Ltd and to exercise the professional, statutory and regulatory accountability required for the licensed manufacturing pharmacy and legal
The primary purpose of this position is to serve as the Responsible Pharmacist (RP) for the company and to exercise the professional, statutory and regulatory accountability required for the licensed manufacturing pharmacy and legal entity in
The application closing date: 29 Sept 2026 Description: The Clinical Trials Unit (CTU) Manager will be responsible for operational oversight, planning, implementation and conduct of assigned clinical trials and in compliance with applicable clinical and regulatory