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Division CMM Department Packaging Employment Type Permanent Job Purpose Monitor and control the operation and running of the packaging machines whilst ensuring adherence to the packaging plan and cGMP Accountabilities Responsible for timeous line start up (minimize down time, increase ouput) Inspection and certification of clean equipment and the completion of the relevant production documentation in accordance with the relevant SOP'S (logbooks, checklist sheet, performance measures) Strip down and cleaning of equipment according to production documentation and SOP's Assembly and operation of equipment according to production documentation and SOP's Storage preparations of cleaning and sanitizing solutions according to SOP's Maintaining stock levels of consumable items thereby ensuring availability for the use in production Ensuring availability of cleaning agents Cleaning of wall panels, floors, windows, auxiliary equipment as per relevant SOP Conduct start up checklists and regular I.P.C check according to SOP's and as specified in the production documentation Setting up machine including change over Ensure adjustments settings on machine to ensure quality product produced efficiently All work/operation must be carried out as per condition stipulated in the OHS ACT (working safely) Carry out work related instructions that are issued by the Supervisor Pharmacist according to the relevant documentation e.g BMR/BPR, SOP's protocols or QA approved documentation Report deviations (Quality and work related) immediately to your supervisor/IPC inspector and shift pharmacist Reports breakdowns immediately to Supervisor and pharmacist Ensure breakdowns are timeously attended to by liaising with the fitter/supervisor Participate in production Optimization (minimise waste, quick change over, identification and resolve delays/ constraints before they occur, contribute to downtime minimization ensure that all material/documents tools and equipment are available Participate in training and development programmes and or assist in training of peer trainees (new staff) Is responsible for carrying out line set up process and must ensure accuracy and correctness of all material issued to a job as per BMR/BPR and Syspro document Ensure functional integrity and safety of machine before use and report any abnormality or defect immediately to your Supervisor/Pharmacist Report component that are of in consistent quality and defects immediately to supervisor, IPC inspector and or shift pharmacist Timeous and correct filing in of information on relevant documentation Operation of machine as per good engineering practices Continuous monitoring of quality of products to ensure specification as per Quality Standards are met, and reporting any deviations immediately To be competent in operational, cleaning of equipment as per SOP Complete practical assessment and to be found competent Conduct shift handover between operators (to arrive 10 minutes before start of shift on line to communicate with operator) Timeous and correct filing in information on relevant documentation document e.g BMR/BPR Logbooks etc. SOP's and protocols or QA approved document log books verification line diaries NB: Full JD available on request Education Qualification Matric/ Grade 12 (with Mathematics & English) Added Advantage: National Diploma in Mechanical or Electrical Engineering or equivalent Relevant Work Experience 1-3 years relevant experience in a Pharmaceutical Industry Job Location Mobeni Shift Hours 06:00 -14:00 14:00 -22:00 22:00 -06:00 Apply Now

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