Orfema Pharmaceutical Industry
Orfema Pharmaceutical Industry Limited offers a wide range of healthcare and Pharmaceutical products. We import and market pharmaceutical Raw materials within other manufacturers of medicine in Nigeria and beyond. We import and market finished pharmaceutical medicines in Nigeria.
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.
To apply, please visit the following URL:https://www.myjobmag.com/a_fields.php?id=593593→