who is outgoing and hard working to fill a Documentation Coordinator role. R 20 000 PM - R 30 000 PM responsibilities, but not limited to: Responsible for all documentation instructions to forwarder Create/ update customer terms of documentation statuses & tracking Responsible for all pre-loading documentation from customers of clearance documentation to customers for approval Tracking of original documentation to customers qualification A minimum 3 years' experience with documentation in the same / similar industry Excellent computer
seeks a suitably qualified, experienced and driven Document Controller to assist in driving the accurate, timeous processing of drawings and documents to site teams, clients and third parties. The tasks you'll project's document management system, Control, coordinate and distribute all project documentation and data control over all design deliverables and technical documents to both Company and ISO 9001 standards. Manage Manage and expedite supplier deliverables and documentation, ensuring contractual requirements are adhered
medical devices and drugs and develop policies for review and sign-off Communicate and liaise with identified related to area of specialisation Continuously review cost / benefit and Return on Investment within development inclusive of Health Technology Assessment documentation compilation; Medicine management policy for market access teams. -Medicine list development and review, including engagement with internal and external industry experience Preferable: formal training in review of evidence-based medicine, particularly in the
pharmaceutical company is looking to employ a Compliance Pharmacist in the Western Cape. - To ensure that the Pharmacy inspections in the Warehouse, office departments and document findings - Liaise with departmental managers on regulations - Gather all necessary support documentation, including SOP's for Pharmacy inspections - Health and Safety - House Keeping audits are documented and deficiencies actioned - SAPC Self Inspections
who is outgoing and hard working to fill a Documentation Coordinator role. R 20 000 PM - R 30 000 PM responsibilities, but not limited to: Responsible for all documentation instructions to forwarder Create/ update customer terms of documentation statuses & tracking Responsible for all pre-loading documentation from customers of clearance documentation to customers for approval Tracking of original documentation to customers qualification A minimum 3 years' experience with documentation in the same / similar industry Excellent computer
dossier compilation required. includes Formula Reviews, toxicology warnings, Artwork, PI/PIL etc. In particular different territories. The position will suit an RA Pharmacist with at least 2 to 3 years of solid RA dossier distributes, and exports it's own products. RA: Formula reviews, labelling, toxicology warnings, impact assessment products is preferred, but not required (RA pharmacists with a desire to learn about RA for CAMS and welcome to apply). B.Pharm degree 2 - 4 years of RA Pharmacist experience compiling dossiers on Extedo, docuBridge
quality standards. Responsibilities: Review of Translated Content: Review and correct translations to ensure sophisticated AI tools. The crucial part is to review the translation, so it looks as it was totally Medium knowledge of Spanish is desirable, though. Review voiceovers to ensure clarity, correct pronunciation feedback to make necessary adjustments. Perform final reviews of new content. Job Requirements: Education and years of experience in translation, translation review, e-learning product quality control, or similar
sector, has an opportunity for an experienced QA Pharmacist (batch release and general QA functions). General manufactured products. • Review batch manufacturing, packaging, and laboratory documentation to ensure that production Conduct annual product quality reviews. • Record and report product quality review data. • Management of reference facilitating strategic, technical, QMS, and/or management review meetings. • Handling and actioning non-conformances and batch manufacturing documents. • Review, update, and maintain master documents, standard operating procedures
pharmaceutical company is seeking a Production Pharmacist who will be responsible to ensure: Safety by QMS /Cipla compliance, maintain RFT process/documents standards, and have no critical/major findings production activities in conjunction with required document-based activities Prepare for daily operations and ready for use as per relevant SOP Ensure documentation/materials are checked as per SOP Ensure sign equipment and areas Authorisation of production documents Initiate operational action to prioritise shift
that, the role will involve general production pharmacist duties, as well as evolving into QA and QC functions