Job Description / Responsibility
• Ensure all GMP related activities throughout the facility.
• Ensure product quality in all steps.
• Ensure training of all employees’ works in the facility.
• Ensure self inspection / internal audit.
• Handling of Incidence, Deviation, Out of Specification (OOS), Out of Trend (OOT), Change Control and CAPA.
• Ensure Validation & documentation always updated in the facility.
• Ensure IPC activities in both manufacturing and packaging line.
• Ensure batch release in local and overseas market etc.

Job Nature
Full-time

Educational Requirements
M. Pharm / M.Sc. in Bio Chemistry / Chemistry.

Experience Requirements
• At least 10 year(s)

Job Requirements
• At least 10 years practical experience in QA department of any reputed pharmaceutical company
• Ability to handling of Market Complaint / Recall.

Send your CV to hrd@somatecpharmabd.com