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 are to be done, as per the requirement of HOD, by

following HODs instructions and guidance