registration process is required. Effectively managing, auditing and implementation of Regulatory systems Key Requirements: experience across the product development, commercialization, and life-cycle maintenance. Knowledge of
registration process is required. Effectively managing, auditing and implementation of Regulatory systems Key Requirements: experience across the product development, commercialization, and life-cycle maintenance. Knowledge of
other relevant standards. Audits and Inspections: Conduct internal audits to ensure compliance with SOPs teams to support product development and commercialization. Continuous Improvement: Identify opportunities
other relevant standards. Audits and Inspections: Conduct internal audits to ensure compliance with SOPs teams to support product development and commercialization. Continuous Improvement: Identify opportunities
division - Drive research, development, and commercialization of space technologies - Ensure financial sustainability new technologies and knowledge solutions Commercialization: Identify market opportunities for SANSA's scientific and technological innovations Drive the commercialization of products and services Stakeholder Engagement: Demonstrated ability to drive innovation and commercialization Outstanding communication and stakeholder
experience to apply for this stimulating position Audit a process [Internal / External] or Quality Management automotive process approach would be required for all audits conducted. Read, understand and interpret technical tools Formal Quality Qualifications in System Auditing Automotive / Technical background and suitable computer literate. Be familiar with and be able to Audit Core Tools Activities. Quality Management systems systems experience Ideal candidate should be able to Audit a process or Quality Management system correctly
or enhanced. Support activities such as internal audits or regulatory agency inspections Ensure alignment experience across the product development, commercialization and maintenance lifecycle Sound project management
ISO 13485 medical devices into the QMS. Co-audit local audits, generate/review reports, and close findings GMP auditing/ ISO 13485 auditing experience (advantageous). Experience with self-inspection audits/ SAHPRA
ISO 13485 medical devices into the QMS. Co-audit local audits, generate/review reports, and close findings GMP auditing/ ISO 13485 auditing experience (advantageous). Experience with self-inspection audits/ SAHPRA
Environmental awareness training and training on conducting audits. Coordinate and chair regular meetings with safety Prepare plants for SABS audits Ensure relevant legal compliance Arrange internal audits Arrange surveys ( Occupational disability management Conduct factory visits and audits Ensure files up to date Intranet checked regularly organized Excellent knowledge on how to conduct audits Relevant post Matric qualification in Environment