Responsibilities
To give line clearance for area and equipment for manufacturing and packing.
To ensure that gowning and entry / exit procedure are followed.
To carry out in process checks in production departments.
To calibrate, maintain the calibration records and general maintenance of instruments:
To assist the Departmental Head to prepare the standard operating procedures and implement systems as per GMP requirements review and verify the log books of equipments/instruments.
To have good relationship and co-ordination with other colleagues working within the department and other departments.
To report daily to the superior to appraise about activities carried out, any deficiencies observed and appropriate corrective action taken or to be taken.
To carry out any further function given by your superiors from time to time.
To prepare the master BMR/BPR for products.
Prepare the Annual product Quality Review for the products manufactured in the facility.
To issue and copy control of standard operating procedures and maintenance of its relevant documentation.
To issue and copy control of batch documents, formats, protocols, labels, log books and maintenance of relevant documentation.
To verify the batch manufacturing and batch packing records for its completeness.
To store and retrieve documents related to Standard Operating Procedures, Master Validation Plan, Site Master File and Other GMP documents.
To maintain, store and retrieve the training records of all personnel.
To maintain the control samples (Retention Samples) of finished products and active starting materials. To destroy retention samples after completion of retention period and maintain the relevant records.
To have good relationship and co-ordination with other colleagues working within the department and other departments.
To report daily to the superior to appraise about activities carried out, any deficiencies observed and appropriate corrective action taken or to be taken.
To carry out any further function given by your superiors from time to time.
Department: Quality Assurance
Job Requirements
Educational Qualification:
Total years of experience:
How to Apply
Interested and qualified applicants should send their CVS via email: yonas.a@africurepharma.com\adisu.genene@africurepharma.com
