Quality Control Officer needed at Orfema Pharmaceutical Industry

Job Description

• You are to ensure Good Clinical Practices (GCP), GMP or GDP in the factory.
• You are to ensure that the relevant quality systems are updated with all required information and action on a timely basis (Ensure timely update of Company quality systems).
• Reviewing of QA controlled documentation (such as SOPs, Batch Records, Quality Manual, Working Instructions, etc.)
• Reviewing and preparing batch release documentation.
• Support audits and inspections to ensure compliance with activities for GMP/GDP.
• Assist with complaint handling activities in line with Company and reporting policies level of investigation to the QAM.
• Organize and administer change control and process change control requires.
• Tracking Non-Conformance reporting activities by the processing of Non-conformance reports and the reviews of the timelines for Corrective and Preventive Action (CAPA) to ensure on time completion.
• Reviewing documentation relating to raw materials and the release of raw materials, repackaging/re-labeling operation.
• Assist product quality investigations and support follow up on established action to address product quality compliance issues identified when product is in the market place.
• Any other job that may be assigned to you from the Management.