Ahlcon Parenterals (India) Limited, a B. Braun group company, located at Bhiwadi, Rajasthan is a major pharmaceutical formulation manufacturer of both Large and Small Volume Parenterals (LVP and SVP) for domestic as well as export markets. We commit to a Zero Defect Quality policy, made possible through the use of technologies and processess that ensure the delivery of high quality products and compliance to Current Good Manufacturing Practices. We also commit to sustainability efforts around our facilities and ensure compliance to global ISO standards.
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Key Responsibilities: Following are the job descriptions but not limited to & applicable for both production block (INA1 & INA4): · Handling of QMS - CAPA, Change Control, Deviation, Investigation, Impact Assessment and FMEA (Failure mode and effective analysis) of related area. · Document preparations like SOP, Protocols, Qualification and URS (User requirement specification). · Coordinate to provide all necessary support to respective person of the area who initiate the observed incident, raised deviation, Change control and other QMS related documents. · Responsible for closing of non-conformance, complies of Audit query and perform validation in production and packing area with QA team. · To ensure GMP, GDP and Data reliability at shopfloor. · To prepare and review the instructions relating to production operation and ensure their strictly implementation. · To evaluate proposed changes in product, process or equipment and ensure that appropriate validations are done. · Review of statistical data of all the machines (Break-down, process loss, rejections, yield, review, corrective & preventive actions). · Shift Production planning, Manpower allocation planning, shift allotment, & Leave management of respective shift officers & operators. · Responsible for other activity related to Manufacturing. · Any other activity or project allocated by the HOD. |
To know more about Ahlcon Parenterals you can visit our website https://www.ahlconindia.com/en.html