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