Assistant Manager/Deputy Manager Manufacturing Oncology

To follow the safety rules in the premises according to the company norms.

•Responsible for production plan, inventory and timely delivery from production to packing.

•Responsible to carry out all activities in manufacturing area in compliance with cGMP.

•Daily work allocation to supervisor & workmen. Achieving set targets of daily/weekly /monthly

manufacturing/packaging plan

•To discuss production plans with team mates and scheduling weekly plans / allocation of weekly shift

schedule.

•Control on GMP documents /log books and other relevant documents of manufacturing

•To review of documents like log books, BMR, BPR for error free online documentation and timely

submission to QA.

•To manage the troubleshooting activity, ensuring identification of appropriate corrective measures and

driving structured implementation of these measures through cross-functional teams.

•To propose and implement innovative ideas towards improvements in process efficiency, productivity,

delivery, quality, yield, safety resulting in successful operations

•To co-ordinate with all concerned departments for providing cost efficient services and achieving

excellence

•To interact with warehouse / QC/ QA for the material availability / release and schedule the production

plan.

•Responsible to maintain the stock of consumables for respective area and follow-up with vendors for

inventory procurement.

•Follow-up with engineering for preventive maintenance & any breakdown

•Control on destruction / disposal of rejects; waste generated during processing.

•Performing equipment qualification and media fill validation along with Validation Team.

•Initiation and closure of change control and CAPA with the stipulated timeframes

•Compliance to the regulatory requirements with respect to the investigations.

•To impart continuous training to the workforce for enhancing their productivity & operational efficiencies

through knowledge enhancement / skill building

•To perform Gap analysis of defined procedures in Batch Manufacturing Record / Batch Packing Record /

Standard Operating Procedure / Protocol and initiation of corrective actions.

•To 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

•Activities other than defined in the job responsibility & allocated by HOD

 

Qualification - B.Pharmacy / M.Pharmacy

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.