upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement ISO standards too facility, to ensure the company will pass a SAHPRA audit. (They are licenced for certain products, but want
upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement ISO standards too facility, to ensure the company will pass a SAHPRA audit. (They are licenced for certain products, but want
upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement ISO standards too facility, to ensure the company will pass a SAHPRA audit. (They are licenced for certain products, but want
have no critical/major findings post inspections/ audits The right people are employed and utilised in the generated and implemented as and when required: Be accountable for shift production and translating targets approval of change request has been obtained Accountable for product and data integrity Writing up of controls Conduct regular internal and external audits Review and improve current documents (BMR/BPRs etc. during all production processes (reconcile, audit, queries resolved before QA review Responsible for
QC Supervisor
Operations
Accountable for specialist outputs and initiating changes in effective chemical management.
Key Accountabilities and Outputs
Supervision
Supervision Safety/Health & Safety
Internal Auditing - conducts routine GMP audits. Enforces Food Safety compliance
ISO standards Preparing batches and documents for audits You need at least one full year of pharmaceutical
team members. Report findings of quality control audit to the Project Manager. Troubleshoot food safety
ISO standards Preparing batches and documents for audits You need at least one full year of pharmaceutical
regulations and standards. Audits and Inspections: Conduct regular SHEQ audits and inspections to identify