- To review, develop and introduce systems, practices and cultural changes that enable the production
department to meet business demands within agreed time frames and expected GXP standards.
- To prepare production planning on monthly basis as per the production requirement and availability of
materials.
- To discuss production plans with subordinates and scheduling weekly plans / allocation of weekly shift
schedule.
- Daily work allocation to supervisors & workmen. Achieving set targets of daily/weekly /monthly
manufacturing/packaging plan.
- To interact with Warehouse/QC/QA for the material availability / release and schedule the production
plan.
- To propose and implement creative ideas towards improvements in process efficiency, productivity,
delivery, quality, yield, safety resulting in successful operations.
- To manage the troubleshooting activity, ensuring identification of appropriate corrective measures and
driving structured implementation of these measures through cross-functional teams.
- To perform Gap analysis of defined procedures in Batch Manufacturing Record / Batch Packing Record /
Standard Operating Procedure / Protocol and initiation of corrective actions.
- To impart continuous training to the workforce for enhancing their productivity & operational efficiencies
through knowledge enhancement / skill building.
- To ensure effective execution of recent product introduction and technology transfer of any product to the
Site.
- To prepare & review of SOPs related to production department.
- To review of documents like log books, BMR, BPR for error free online documentation and timely
submission to QA.
- To co-ordinate with all concerned departments for providing cost efficient services and achieving
excellence.
- Planning and execution of media fill validation along with Validation Team.
- To ensure timely execution of equipment qualification along with Validation Team.
- To review the annual validation plan, preventive maintenance plan and calibration plan.
- Ensure timely initiation and closure of QMS documents of production department like change control,
deviations, CAPA and Risk Assessments with the stipulated timeframes.
- To involve and implement in self-inspection of the system and use the findings from such audits for
overall improvement of facility, systems and documentation process.
- Compliance to the regulatory authorities with respect to the investigations.
Qualification - B Pharma / M Pharma
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.