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At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Key responsibilities:
- To Maintain discipline and co-operate to all the members working in factory.
- To maintain shift schedule time to time as per instructions provided by immediate supervisor.
- To follow good hygienic practices, safety rules and respective gowning procedure.
- To follow c-GMP practices.
- To Participate and supervise the area activities like
- Production Area Maintenance.
- General Area (CNC) daily routine activity.
- General area Cleaning and Sanitization.
- Batch manufacturing and filtration activity.
- Passivation activity
- Disinfectant solution preparation, filtration and reconciliation activity.
- Classified area daily, weekly and monthly activity
- Clean Area related activities.
- Garment washing area related activities.
- Aseptic Manufacturing related activities.
- EDMS related activities.
- SAP related activities.
- Equipment qualification.
- Area qualification.
- To prepare protocol as per the process requirement.
- To co-ordinate with other supervisor of area of and of other department as per routine production planning.
- Online documentation related to Work Area, BMR etc.
- To report deviation, abnormal observation during day-to-day activities to immediate supervisor.
- To impart necessary training/ instructions to sub-ordinates related to the area of working.
- To fulfil the activities instructed by Superior from time to time.
- To ensure status label is attached and updated on area/ equipment /services / product of related area at each stage.
- To intimate engineering department for machine breakdown & follow up to put machine back into the operation.
- To ensure storage of the filled products at the quarantine area or as per the defined storage condition and to maintain their records.
- Reporting of day to day activities to the superior with specific highlight to important issues & development activities.
- To prepare and execute the qualification protocol as per QMP.
- To prepare the risk assessment of equipment and process.
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