Job Description

oTo follow the safety rules in the premises according to the company norms. oResponsible for production plan, inventory and timely delivery from production to packing. oResponsible to carry out all activities in manufacturing area in compliance with cGMP. oDaily work allocation to supervisor & workmen. Achieving set targets of daily/weekly /monthly manufacturing/packaging plan. oTo discuss production plans with team mates and scheduling weekly plans / allocation of weekly shift schedule. oControl on GMP documents /log books and other relevant documents of manufacturing. oTo review of documents like log books, BMR, BPR for error free online documentation and timely submission to QA oTo manage the troubleshooting activity, ensuring identification of appropriate corrective measures and driving structured implementation of these measures through cross-functional teams. oTo propose and implement innovative ideas towards improvements in process efficiency, productivity, delivery, quality, yield, safety resulting in successful operations. oTo co-ordinate with all concerned departments for providing cost efficient services and achieving excellence. oTo interact with warehouse / QC/ QA for the material availability / release and schedule the production plan. oResponsible to maintain the stock of consumables for respective area and follow-up with vendors for inventory procurement. oFollow-up with engineering for preventive maintenance & any breakdown. oControl on destruction / disposal of rejects; waste generated during processing. oPerforming equipment qualification and media fill validation along with Validation Team. oInitiation and closure of change control and CAPA with the stipulated timeframes. oCompliance to the regulatory requirements with respect to the investigations. oTo impart continuous training to the workforce for enhancing their productivity & operational efficiencies through knowledge enhancement / skill building. oTo perform Gap analysis of defined procedures in Batch Manufacturing Record / Batch Packing Record / Standard Operating Procedure / Protocol and initiation of corrective actions. oTo review, develop and introduce systems, practices and cultural changes that enable the department to meet business demands within agreed time frames and expected GXP standards. oActivities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HODs instructions and guidance



B. Pharmacy / M. Pharmacy with 5-7 years experience in Filling & Sealing area experience.



Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.