About this role
<div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px">Job Description</H2> </div><div><p>Department: Production<br> Designation: Associate- Production <br> Working Section: Granulation, Compression, Coating and Encapsulation</p> <p> Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements.<br> Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task.<br> Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers. <br> Report any quality concern or suggestion for improvement to supervisors/ managers.<br> Manufacturing / processing of batches of assigned products under supervision as per instructions given in the BMR.<br> Handling and movement of raw material, bulk, semi-finished and finished goods.<br> Operation, washing and cleaning of equipment’s and accessories used in related production activities as per respective SOP.<br> Up-keeping area and machines as per GMP requirements.<br> To Support Quality Management Systems and to report any discrepancy, abnormity, non-conformance or any incidence observed to the Department Head and QA Head.<br> Receipt of RM and PM from Warehouse and ensuring overall cleanliness of areas.<br> Doing operations as per the SOPs and BMR with online recording in respective documents as applicable.<br> To ensure self-hygiene before entering in the production area and follow all the other rules & regulation set by HR department.<br> Performing in-process checks as per respective BMR and recording of results of in respective documents as applicable.<br> To fulfil the training need as per current needs with respect to cGMP, Job, safety, health & Hygiene by attending the training programmes.<br> Cost effectiveness in production operation by controlling overtime, revenue expenses and achieving standard yield.<br> Critically monitoring of the environmental conditions with a view to meet the standards mentioned in BMR and SOP.<br> Ensure calibration and preventive maintenance of manufacturing equipment and instruments as per approved schedule and the results of same meeting the standards.<br> To perform line clearance activity during batch to batch and product to product change over and ensure the compliance as per SOP.<br> Issuance, retrieval and destruction of dies and punches, product dedicated bags and sieves, silicon sleeves, pipes, hose pipes and screens.<br> To ensure the audit compliance.<br> Trouble-shooting: To attend the problems of machine and process as and when necessary.<br> Any other assignment allocated by production Head.<br> To attend required cGMP/ On Job /Functional training activities as per planner.<br> </p> </div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px">Work Experience</H2> </div><div><p>2 to 5 years</p></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px">Education</H2> </div><div><div>Diploma in Pharmacy</div></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px">Competencies</H2> </div><div><div>Innovation & Creativity</div><div>Result Orientation</div><div>Collaboration</div><div>Customer Centricity</div><div>Developing Talent</div><div>Stakeholder Management</div><div>Strategic Agility</div><div>Process Excellence</div></div></div></div>