Job Description :

• Collect, format, modify, follow up all preparing SOPs / modification SOPs of Industrial Quality & Compliance and Industrial Affairs in compliance with Corporation’s, GMP and ISO regulations
• Assist the Quality Unit in translating.
• Manage, archive original copies of current procedures and superseded procedures as required; distribute copies of current procedures to related department.
• Collect, cancel all old procedures according to the procedures on document managing.
• Update the procedures still bearing the RPR logo or procedures having no more place for extension of expiry date in collaboration with different departments
• Combine the user requirements of raw and packaging materials with the test methods
• Modify the process validation according to the concerned manufacturing process.
• Prepare & enter the data of BMR

• Pharmacist degree
• At least 1 year experience ...