Responsible for the in-process quality of all products manufactured.
Key Tasks
all products / test / trials conducted on materials and
reports / feedback as requested by Management on all activities.
administrative activities such as checking and completing all QA and QC documentation. REQUIRED MINIMUM EDUCATION Effective written and verbal communication with all interested parties (internal & external). SHEQ (PQMP) according to Client requirements. Obtain all necessary product acceptance and product release requirements. Obtain the signatures of all parties involved on all quality related documentation. Review nonconformance system. Ensure document and record control of all quality related documentation (M-Files and hardcopy
walkabout inspections for the purpose of identify all hazard exposures and their associated risks. · Formulate ensure they all bear correct Legal References · Consolidate all risk assessments for all NWU Campuses incidents trends. · Assign investigators. · Evaluate all investigation. · Co-ordinate creation of an action in doing high level SHE Inspections and audits on all campuses. · Monitor activities and operations and Reports from all inspections with OHS coordinators. · Follow up on the implementation of all recommendations
walkabout inspections for the purpose of identify all hazard exposures and their associated risks. · Formulate ensure they all bear correct Legal References · Consolidate all risk assessments for all NWU Campuses incidents trends. · Assign investigators. · Evaluate all investigation. · Co-ordinate creation of an action in doing high level SHE Inspections and audits on all campuses. · Monitor activities and operations and Reports from all inspections with OHS coordinators. · Follow up on the implementation of all recommendations
responsible for:
Ensure all incidents and accidents are reported and correct documentation completed. Ensure all identified assessments, procedures, and work instructions. Ensure all H&S lawful requirements are met and adhered to
Ensure all incidents and accidents are reported and correct documentation completed. Ensure all identified assessments, procedures, and work instructions. Ensure all H&S lawful requirements are met and adhered to
and existing product Provide effective feedback to all relevant departments, if dimensional deviations or audits Calibration – Maintain calibration status of all existing gauges and instruments – inclusive of physical in accordance with works instructions, as well as all relevant documentation. Manage external calibration
to stakeholders and in the correct format. Manage all Final product manufacturers, Final Release Laboratories quality systems to ensure quality products Ensure that all Manufacturers, Laboratories, Warehouses and Distributors in place to maintain the positive GMP status of all Manufacturers, Laboratories, Warehouses and Distributors that Quality/Technical agreements are in place for all our products Manage and facilitate artwork projects Quality Systems and ensure that the SOP's are guiding all personnel in a clear and understandable manner Support
to stakeholders and in the correct format. Manage all Final product manufacturers, Final Release Laboratories quality systems to ensure quality products Ensure that all Manufacturers, Laboratories, Warehouses and Distributors in place to maintain the positive GMP status of all Manufacturers, Laboratories, Warehouses and Distributors that Quality/Technical agreements are in place for all our products Manage and facilitate artwork projects Quality Systems and ensure that the SOP's are guiding all personnel in a clear and understandable manner Support