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