supplier's list. Internal and External Audits and any deviations are followed up. Liaise with service providers responsibilities. Implement a Stability Master Plan. Experience in Medical Devices 2. COMPLAINTS To ensure that correct manner, the reason for returns determined, and any further actions followed through and recorded. To Final decision to re-analyze, re-pack, or destroy any returned/rejected goods. 5. GMP/GWP/GHP To ensure self-inspection / internal audits are performed, and any deviations followed up. To ensure all external service
supplier's list. Internal and External Audits and any deviations are followed up. Liaise with service providers responsibilities. Implement a Stability Master Plan. Experience in Medical Devices 2. COMPLAINTS To ensure that correct manner, the reason for returns determined, and any further actions followed through and recorded. To Final decision to re-analyze, re-pack, or destroy any returned/rejected goods. 5. GMP/GWP/GHP To ensure self-inspection / internal audits are performed, and any deviations followed up. To ensure all external service
strictly according to applicable methods as provided. Any deviations must be authorised by the QA Manager and and Safety policy is applied effectively.
communicate issues to the Production Manager. Record any unsterile runs in the spreadsheet and communicate and/or signing off of SOP's, standard forms and any additional documentation relating to quality, improvement testing is required or space becomes an issue. Prepare any samples that need to be sent for sterility and Bioburden following procedures during production. Identify any training needs for all Quality Controllers. Ensure Matric/Grade 12 Basic Microbiology Minimum Experience 3-5 years of experience in the laboratory / medical device
years' experience in Regulatory Affairs, preferably in human medicines - Demonstrable experience across deliver to quality, time and cost standards - Experience in use of CTD software builder and compilation
years' experience in Regulatory Affairs, preferably in human medicines - Demonstrable experience across deliver to quality, time and cost standards - Experience in use of CTD software builder and compilation
required
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Must have working experience in fragrance development and application. Experience in managing raw material
1 to 3 years of QA experience, preferably at a CAMS company. Deputy RP experience is an advantage, not will be affected by specific years of relevant experience, as well as specific qualifications etc. A salary