apply for the Independent Contractor position of Clinical Evaluator to be based at Beier Drawtex Healthcare for preparing Clinical Evaluation Plans, Clinical Evaluation Reports, Post Market Clinical Follow Up Reports other clinical documentation as required for CE marked devices Responsible for writing Clinical Investigation Investigation Plans Provide clinical input into product development projects Consistently provide feedback feedback on updates to clinical regulatory requirements and related standards / guidelines Relevant medical
apply for the Independent Contractor position of Clinical Evaluator to be based at Beier Drawtex Healthcare for preparing Clinical Evaluation Plans, Clinical Evaluation Reports, Post Market Clinical Follow Up Reports other clinical documentation as required for CE marked devices Responsible for writing Clinical Investigation Investigation Plans Provide clinical input into product development projects Consistently provide feedback feedback on updates to clinical regulatory requirements and related standards / guidelines Relevant medical
The Clinical Laboratory Operations QA Associate I reports to the Lead Clinical Laboratory Operations responsible for creating, developing, monitoring and managing quality systems that support ongoing Laboratory Laboratory Operations of specimen processing for HVTN clinical trials across Southern Africa. A person in this responsibilities in leading project efforts and management of quality systems. The focus of responsibilities coordinate and facilitate clinical site specimen processing and clinical testing laboratory projects
The Clinical Laboratory Operations QA Associate I reports to the Lead Clinical Laboratory Operations responsible for creating, developing, monitoring and managing quality systems that support ongoing Laboratory Laboratory Operations of specimen processing for HVTN clinical trials across Southern Africa. A person in this responsibilities in leading project efforts and management of quality systems. The focus of responsibilities coordinate and facilitate clinical site specimen processing and clinical testing laboratory projects
passionate and motivated Production Manager to be based in their Hermanus branch
Our client is looking for a seasoned QA Manager to join their team. The ideal candidate will possess measures throughout the manufacturing process.
experienced SHER Manager to oversee and enhance their safety, health, environment, and risk management programs Occupational Health and Safety, Environmental Management, or related field. SAMTRAC qualification is advantages experience as a SHER Manager in the manufacturing industry. Environmental management system qualification comprehensive safety, health, environmental, and risk management policies and procedures. Ensure policies are
requirements are incorporated into the companys Quality Management System.
Identify and coordinate the necessary
Quality, Food Safety, PRPS, GMP and GHP).
Manage the internal audit programme (Audit Plan, Tracking
/>Coordinate external audits and manage actions from these audits.
Manage QA external service providers
(SCS Africa, GOTECH and ECOLAB).
Effective management of QA budget.
Ensure full compliance to
to all users in the roles of a Super User.
Manage the document control, Issues and Audit Database
compliance with safety regulations and manage emergency response programs Manage emergency response program, stay legislative reporting Stay informed on environmental management systems, contribute to environmental policy, and analyze risks Monitors the wearing of PPE and manage training programs to increase safety proficiency Health Participate in accident investigations, manage safety training programs, and implement corrective environmental service contracts, monitor environmental management system, and maintain registers Monitoring the