submit documents as per schedule. Assess and report any deviations to TS/ LM. Evaluate and assess QC according limits. Record QCs as per SOP requirements. Report any deviations from quality control specifications immediately scheduled analysis before testing commences. Report any stock requirements to LM and TS. Advise of increased Validations and R&D initiatives. Feedback to TS/LM on any matters that may affect the functioning of the department Customer Service Inform management immediately of any customer queries or complaints received. Perform
submit documents as per schedule. Assess and report any deviations to TS/ LM. Evaluate and assess QC according limits. Record QCs as per SOP requirements. Report any deviations from quality control specifications immediately scheduled analysis before testing commences. Report any stock requirements to LM and TS. Advise of increased Validations and R&D initiatives. Feedback to TS/LM on any matters that may affect the functioning of the department Customer Service Inform management immediately of any customer queries or complaints received. Perform
reporting to you involved in any process, operation, or activity at any stage of an RB product lifecycle for ensuring the Training Matrix is up to date and any gaps, updates to processes are reported on the KPI
reporting to you involved in any process, operation, or activity at any stage of an RB product lifecycle for ensuring the Training Matrix is up to date and any gaps, updates to processes are reported on the KPI
manufacture, pack, test, and warehouse or distribute any company product Quality system support: Assist with report to the responsible pharmacist and assist in any investigation and proposal of corrective and preventative preventative action. Manage the implementation of any proposed corrective action and provide feedback so products in accordance with GMP requirements and that any Out of Specification (OOS) stability results are
manufacture, pack, test, and warehouse or distribute any company product Quality system support: Assist with report to the responsible pharmacist and assist in any investigation and proposal of corrective and preventative preventative action. Manage the implementation of any proposed corrective action and provide feedback so products in accordance with GMP requirements and that any Out of Specification (OOS) stability results are
exposure and training to the docuBridge software. Any relevant tertiary qualification is sufficient. BSc
exposure and training to the docuBridge software. Any relevant tertiary qualification is sufficient. BSc
blasting operations as needed. - Monitor and report any issues or concerns related to blasting operations
blasting operations as needed. - Monitor and report any issues or concerns related to blasting operations