with quality standards. Visit supplier sites and assist operations by tracking, documenting, and reporting Analyse quality data and generate reports for management. Ensure that manufacturing processes comply with Controls to ensure that spend is appropriately managed and cost saving inititaives identified and initiated complaints. Bachelor's degree in Engineering, Quality Management, or a related field. At least 5 years experience
/>Duties and Responsibilities:
and maintenance lifecycle
collection and trending Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO analysis and trending remarks MEDICAL DEVICE FILE Managing the Group Medical Device File programs and databases documents. Follow up with allocated department Product Managers and Specialists for Product Dashboards and product Trend KPI data and provide report timeously for Management Review RECALLS, FIELD SAFETY ACTIONS AND ADVERSE data and provide report timeously for Management Review. ASSISTANCE WITH SAHPRA APPLICATIONS Support in
collection and trending Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO analysis and trending remarks MEDICAL DEVICE FILE Managing the Group Medical Device File programs and databases documents. Follow up with allocated department Product Managers and Specialists for Product Dashboards and product Trend KPI data and provide report timeously for Management Review RECALLS, FIELD SAFETY ACTIONS AND ADVERSE data and provide report timeously for Management Review. ASSISTANCE WITH SAHPRA APPLICATIONS Support in
collection and trending
Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO
/>
MEDICAL DEVICE FILE
Managing the Group Medical Device File programs and databases
/>Follow up with allocated department Product Managers and Specialists for Product Dashboards and product
/>Trend KPI data and provide report timeously for Management Review
RECALLS, FIELD SAFETY
provide report timeously for Management Review.
ASSISTANCE WITH SAHPRA APPLICATIONS
operational” overseeing and professional OHS management system thereby ensuring that the Company operates (Combined Code) of practice pertaining to OHS Management, Including Famous Brands Safety Policy and Standards documentation as per FB and legal requirements. Manage internal self-audits and analyze findings and monitor and sustain the Safety through FB Internal OHS management system and NOSA grading system, Attending daily aligned to the TOR, Empower operators and line managers to be able to provide an encompassing leadership
operational” overseeing and professional OHS management system thereby ensuring that the Company operates (Combined Code) of practice pertaining to OHS Management, Including Famous Brands Safety Policy and Standards documentation as per FB and legal requirements. Manage internal self-audits and analyze findings and monitor and sustain the Safety through FB Internal OHS management system and NOSA grading system, Attending daily aligned to the TOR, Empower operators and line managers to be able to provide an encompassing leadership
international regulations. Product Registration: Manage the process of registering new products or updating Duties Quality Systems Management: Develop, implement, and maintain quality management systems (QMS). Ensure SOPs and regulatory requirements. Prepare for and manage external inspections by regulatory agencies. Documentation: processes and activities. Deviation and CAPA Management: Investigate deviations and non-conformances relevant regulatory and quality practices. Risk Management: Conduct risk assessments to identify potential
international regulations. Product Registration: Manage the process of registering new products or updating Duties Quality Systems Management: Develop, implement, and maintain quality management systems (QMS). Ensure SOPs and regulatory requirements. Prepare for and manage external inspections by regulatory agencies. Documentation: processes and activities. Deviation and CAPA Management: Investigate deviations and non-conformances relevant regulatory and quality practices. Risk Management: Conduct risk assessments to identify potential