The administration and management of the site's Quality function ensuring the products exceed customer Implementation of a continual, periodic review of ISO systems with EHS practitioner. Develop and manage raw materials Practitioner when not on site ISO 9001 Quality Management system Min 3 years COAs External Auditors experience is
breakdowns Support engineering projects Maintenance Administration Minimum Requirements: Tertiary Qualification
breakdowns Support engineering projects Maintenance Administration Minimum Requirements: Tertiary Qualification
adhering to the ISO 17025:2017 quality management system designed for Laboratories. Furthermore, the technician technician assists in Laboratory administration and operation in regard to master calibration and permit Ensuring compliance with Laboratory Quality Management System (QMS) and ISO 17025: 2017 accreditation requirements Offer where nuclear gauges are involved. Quality Systems Support Maintain and support the ISO 17025:2017
adhering to the ISO 17025:2017 quality management system designed for Laboratories. Furthermore, the technician technician assists in Laboratory administration and operation in regard to master calibration and permit Ensuring compliance with Laboratory Quality Management System (QMS) and ISO 17025: 2017 accreditation requirements Offer where nuclear gauges are involved. Quality Systems Support Maintain and support the ISO 17025:2017
have 5yrs Experience in Quality in Food Safety Systems interface (FSSC 22000, ISO 9001, ISO 14001) and Management. Design, Implement and management of QA Systems, Company Global Standards and Legislation requirements requirements are incorporated into the QA System. Exp on Achiever Plus, Quality, Food Safety, PRPS, GMP and
and to maintain the product, process, quality and system to agreed standards through facilitation of improvements Process Auditor, System Auditor or Product Auditor). Key Performance Areas: System and Process Compliance: Compliance: Assist in maintain an integrated quality system structure within BRMP (Business Risk Management Programme) management structure. Perform audit of the systems, processes and products on site to a defined audit Evaluate daily and report on the Customer performance systems of any concerns raised. Control all quality-related
Regulatory Affairs pharmacists with the day-to-day administrative RA tasks. Faxing, filing, liaising with various
Regulatory Affairs pharmacists with the day-to-day administrative RA tasks. Faxing, filing, liaising with various
Production Manager Capture all relevant data on the system Final Product Ensure finished product conforms