Tshwane Metro, Pretoria, Brooklyn
Permanent, full-time hours
Health, Medical and related
Insurance
A relevant cli
The main job purpose is to ensure the compliance of pharmaceutical products with regulatory requirements in South Africa and other designated markets. This role involves managing regulatory submissions, writing and reviewing Chemistry, Manufacturing, and Controls (CMC) documentation, and maintaining
Job Summary: To ensure that Inspections systems are functioning correctly and that all quality control processes are producing the product that meets specified requirements and leads the team. Main Responsibilities (not limited to): •To ensure compliance to defined quality standards •To perform
JUNIOR TECHNOLOGIST Location: Roodeplaat Offer: R 255 000-00 P/A Type: Permanent Closing date: 20 June 2024 QUALIFICATION ESSENTIAL: B.Sc. / B Tech / Diploma with microbiology, plant pathology, biochemistry or similar as main subjects DUTIES, RESPONSIBILITIES AND AUTHORITIES ADMINISTRATION – aspec
Ref: TMO 416473 - Lab Analyst Employer Description Our client is a laboratory that offers microanalysis, analytical chemistry as well as Research and Development Job Description Responsible for ensuring correct receipt and registration of test items Ensure proper housekeeping is maintained in the la
Ref: TMO 416473 - Lab Analyst Employer Description Our client is a laboratory that offers microanalysis, analytical chemistry as well as Research and Development Job Description Responsible for ensuring correct receipt and registration of test items Ensure proper housekeeping is maintained in the la
Our client in the Medical Devices industry is currently looking for a Research Audiologist , in Pretoria, Gauteng. Audiological research: design and implementation. Report writing and documentation. Fitment of hearing aids. Fine-tuning of hearing aid settings. Customer relations and relationship man
Our client in the Medical Devices industry is currently looking for a Research Audiologist , in Pretoria, Gauteng. Audiological research: design and implementation. Report writing and documentation. Fitment of hearing aids. Fine-tuning of hearing aid settings. Customer relations and relationship man
Reference: PE001006-M -1 Our client is seeking an experienced Quality Assurance Manager to join their company. Requirements: Post-matric studies in quality management systems. Computer literate (MS Office, Lotus Notes, etc.) Bachelor's degree in a relevant field (Quality Assurance, Engineering, Scie
The main job purpose is to ensure the compliance of pharmaceutical products with regulatory requirements in South Africa and other designated markets. This role involves managing regulatory submissions, writing and reviewing Chemistry, Manufacturing, and Controls (CMC) documentation, and maintaining