Job summary
QA Officer will be responsible for ensuring cGMP compliance within the manufacturing facility
Job descriptions & requirements
Responsibilities and Duties
- Preparation, development and review of Standard Operating Procedures.
- Assigning batch number, manufacturing and expiry date to drug products.
- Issuance of batch manufacturing record and batch packing record
- Preparation of master formula record, batch manufacturing record and batch packing record.
- Issuance and retrieval of monthly documents and format to respective department
- Review of preventive maintenance schedule
- Assessment, review and closer of change control and deviation
- Management of corrective and preventive action
- Preparation of annual product quality review
- Specimen signature management
- Incident handling
Qualifications
- Science Graduate
- Minimum of 2 years' work experience with a pharmaceutical industry
- Working knowledge of cGMP is a must.
Salary: GHS 2,400 - GHS 3,000
Location: Accra
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