Website Adcock Ingram
Adcock Ingram is a leading South African pharmaceutical company with a proud 130 year heritage. It has a portfolio of trusted, quality brands and generics and an entrenched value system that assures integrity. Growing from humble beginnings as a small Krugersdorp pharmacy in 1890, Adcock’s portfo… read morelio includes an extensive range of Prescription, Over-the-counter (OTC), Consumer and Hospital products and life saving hospital products.
Key Job Outputs:
Responsible for personnel adherence to current Good Manufacturing Practice (cGMP) and Good Documentation Practice (GDP) requirements, hygiene and good housekeeping.
Compliance with SOPs
Ensure that SOPs training (QA and cGMP) is completed in accordance with the training plan
Ensure that new incumbents are put through induction training.
Initiate, update, review and approve SOPs. Participate in both external and internal inspections:
Ensure that internal audits are conducted as per schedule and that findings are closed on time as per action plan.
Ensure no repeat of the audit findings particularly critical or major findings.
Documentation:
Ensure that the registers forheduled substances (narcotics) are upto-date.
Ensuring completion of Batch manufacturing/packing records prior to submission to QA.
Ensure that registers for the storage rooms where products are kept are up-to-date.
Customer complaints:
Conduct thorough investigation for every received complaint.
Compile a comprehensive report timeously.
Ensure that the CAPAs are implemented.
Complete all records and reports timeously and accurately as described in the relevant SOPs protocols and associated documentation.
Operational activities
Ensure that line opening/clearance, in process checks (IPC) and line closing are done in accordance with SOP.
Ensure that products are produced, packed and stored according to the required SOP and documentation.
Ensure that QMS is followed and adhered to at all times in terms of;
Documentation and investigation of Deviations,
Raising of CAPAs, Change Controls and their timeous closure and effective implementation.
Reporting of non-conformities with respect to both the product and the environmentals as described in the relevant SOPs.
Verify the identity of bulk product and printed packaging material.
Ensure that materials and product are correctly handled, stored and recorded.
Monitor production processes by overseeing critical process parameters of various packaging stages.
Investigate incidents that resulted in non-conforming products.
Ensure that the staff comply with the dress code.
Validation, Calibration and Qualification.
Facilitate and participate in qualification, validation studies.
Ensure effective technology and skills transfer.
Health, safety and environmental standards.
Ensuring that no disabling injuries by ensuring that protective clothing is worn and no machinery poses a safety hazard.
Report any incident which may affect personnel health or cause injury to the SHE representative or line manager.
Carry out any duty or requirements imposed on the company by the OHS Act and in accordance with your specific SHE appointment.
Human recourses (Compliance to labour law).
Ensure that staff are offered the necessary training/skills to carry out their duties effectively and per operational requirements.
Familiarize yourself with company policies and procedures and comply with them at all the times.
Any other function that the manager may delegate from time to time.
Requirements
Grade 12
B.Pharm
Experience in Pharmaceutical/Manufacturing will be advantageous.
Apply via company website ( N / A ) or
adcock.mcidirecthire.com