Please note that our Terms & Conditions and Privacy Notice are applicable.
Medical Officer (x2 - Wits RHI)
1 Photo(s)
4 months ago615 views
General Details
Location:
Advertised By:Agency
Company Name:Executive Placements
Job Type:Full-Time
1
Responsibilities include supporting end-to-end product development (formulation, design controls, validation, documentation, and transfer to production) as well as maintaining existing products to ensure quality, stability, safety, and regulatory compliance in a GMP/ISO 13485 environment. The role involves both collaboration with internal teams and independently managing workstreams.Independent research and product development: Plan, design, execute, and troubleshoot experiments Conduct literature reviews and self-directed research to support product developmentLead the development, optimisation, and validation of formulations, test methods, and processesManage multiple tasks and long-term development projects simultaneouslyTechnical problem-solving and process support Solve complex technical challenges affecting formulations or manufacturingSupport and improve production processes and resolve raw material or process-related issuesPerform material acceptance, supplier evaluations, and introduce new materials/equipment as neededPerform data trending, technical assessments, and stability evaluationsQuality, compliance and documentationMaintain accurate, complete technical documentation in line with QMS requirementsParticipate in product risk management activities, including hazard identification, assessment, and mitigationEnsure controlled documents (procedures, forms, lists) remain accurate and updatedSupport nonconformity investigations and CAPA activitiesRegulatory responsibilities Compile complete dossiers for new products (Technical Files, Design Files, Clinical Evaluation inputs, Biocompatibility inputs) per international standards Ensure existing product dossiers remain updated and aligned with regulatory requirementsSupport CE marking, SAHPRA submissions, and international regulatory activitiesEnsure labelling, IFUs, and end-user information are compliant and currentSupport PMS/PMCF activitiesCross-functional and external support Provide technical input to Quality, Production, and Procurement teamsAssist with technical and scientific client queriesTrain and support staff on testing equipment and technical processes REQUIREMENTS:Tertiary degree in Science or EngineeringMasters degree (MSc/MEng) strongly preferredPostgraduate specialisation in Chemistry/Chemical Engineering advantageousExperience in scientific technical/academic writingExperience in medical device or pharmaceutical deve
https://www.jobplacements.com/Jobs/R/Research-and-Development-Scientist-Engineer-1240480-Job-Search-11-19-2025-6-58-36-AM.asp?sid=gumtree
Invalid date
Job Placements