Job Category: QA
Job Type: Full Time
Job Location: Ja-ela Ekala
To develop efficient filling system of all QA documents by assigning file numbering system, prepare master index, lists of documents and ensure correct filing of documents.
- Preparation of SOPs.
- Preparation & Review of batch manufacturing records and batch packing records.
- Assist in execution of validation and qualification activities.
- Review of filled BMR/BPR.
- To monitor IPQA activities on shop floor.
Qualifications and Experience
- Bsc Science or B.Pharm full qualification.
- 02 -03 years’ experience in a pharmaceutical manufacturing environment.
- Ability work independently by meeting deadlines.
- Must be a good team player with positive attitudes.
- Excellent communication skills in English.
