Associate

Job Description:

Responsibilities

• Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements.
• Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task.
• Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers.
• Report any quality concern or suggestion for improvement to supervisors/ managers.
• Manufacturing / processing of batches of assigned products under supervision as per instructions given in the BMR.
• Handling and movement of raw material, bulk, semi-finished and finished goods.
• Operation, washing and cleaning of equipment’s and accessories used in related production activities as per respective SOP.
• Up-keeping area and machines as per GMP requirements.
• To Support Quality Management Systems and to report any discrepancy, abnormity, non-conformance or any incidence observed to the Department Head and QA Head.
• Receipt of RM and PM from Warehouse and ensuring overall cleanliness of areas.
• Doing operations as per the SOPs and BMR with online recording in respective documents as applicable.

Qualification & Experience

• 2-6 years
• Education
• Diploma in Pharmacy