Associate

Job Description
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.
Packing and documentation of assigned products as per instruction given in the BPR, SOP and cGMP.
Handling the movement of bulk, packing material, semi-finished and finished goods as per SOP.
Maintaining Overall equipment efficiency (OEE)/Productivity.
To up keep cleanliness of area and machine as per GMP requirement.
Operation, washing and cleaning of equipment and accessories used in related production activities as per SOP.
Monitoring and recording of differential pressure, temperature & relative humidity as per SOP.
Ensure calibration and preventive maintenance of equipment and instrument as per approved schedule and the results of same meeting the standards.
Performing in-process checks as per respective BPR and recording of results of in process checks in BPR.
Receipt, issuance, retrieval, maintenance and disposal of change parts.
Area and Equipment Usage documented as per SOP.
To attend the required cGMP/On job/Functional training activities as per planner.
To ensure proper self – hygiene before entering in the production area and follow all the rules and regulation set by HR department.
To initiate and review the request like additional material requisition, material return note, packing material carry forward Stereo request and screen request etc.
To ensure the effective control on usage of manpower, machine and material in the department and maintain proper inventory of operating supplies in the department.
To support Quality Management system and to report any discrepancy, abnormality, non –conformance or any incidence observed to the department head.
Handling of Omnidoc, Data Acquisition system (DAS).
Checking of strip/blister foil proof with batch packing record and also retention of all required packing material proof with batch packing record for packing section.
To attend the trouble shooting of machine.
Trouble shooting: Handling, ensuring, verifying and trouble shooting of software like, Blister inspection system, inkjet coding.
Any additional responsibility delegated by department head.
Work Experience
2 to 5 years of experience
Education
Diploma in Pharmacy
Graduation in Science
Competencies
Strategic Agility
Process Excellence
Innovation & Creativity
Developing Talent
Customer Centricity
Collaboration
Result Orientation
Stakeholder Management

Work arrangement
No