Systems, Documentation Control, Human Recourse, Production, S5 & S6 Controls Highly experienced on and Responsibilities: - Release of finished goods Assist QA Release Pharmacist in the following activities relevant QA reports to contract givers for approval. Assist with product release when required. Documentation by the QMS officer. Assist with marketing and regulatory affairs. Functions Assists QA Manager with overseeing according to the schedule planned. Internal Audits Assists QA Manager with overseeing that internal audits
to the various quality, technical and document control functions within Randburg SHEQ Department. KEY documents such as data books/dossiers, quality control plans, procedures, etc, as required by customers surveillance inspections. Technical Quality: 5. Assist with technical quality specification reviews and measuring, and reporting on various quality data. 8. Assist with quality compliance audits and assessments corrective action processes. Quality Document Control: 10. Document co-ordination, liaison and processing
2 years+ experience in similar role
laboratory administration, including budgeting and cost control Ensure timely delivery of services to internal compliance with cGMP guidelines and manage change controls and NCRs Address facility issues and risks in in collaboration with Engineering Provide assistance and guidance to operational departments as needed development (chemical) and experimental planning Assist with technology transfers from development to manufacturing quality risk management Manage deviations, change controls, and CAPAs Drive quality objectives and ensure
laboratory administration, including budgeting and cost control Ensure timely delivery of services to internal compliance with cGMP guidelines and manage change controls and NCRs Address facility issues and risks in in collaboration with Engineering Provide assistance and guidance to operational departments as needed development (chemical) and experimental planning Assist with technology transfers from development to manufacturing quality risk management Manage deviations, change controls, and CAPAs Drive quality objectives and ensure
facility in Westmead The overall scope of role is to assist the business with research and development of new of the role: Research and Development Quality Control Product Supervision Attend to equipment breakdowns
facility in Westmead The overall scope of role is to assist the business with research and development of new of the role: Research and Development Quality Control Product Supervision Attend to equipment breakdowns
is responsible for implementing the actuarial control function across the licenses and provides actuarial report to the Head: Corporate Actuarial and will assist with the following: Calculation and management
is responsible for implementing the actuarial control function across the licenses and provides actuarial report to the Head: Corporate Actuarial and will assist with the following: Calculation and management
ge or experience of running plant trials in a factory environment