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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:
- Preparation / Initiator sign authority for :
- Commercial product / stability batches / exhibit batches / characterization batches– Master Batch Manufacturing Record.
- Risk Assessment, process Validation protocol, incident and investigation report, action, compliance, and closure.
- CAPA plans and closure.
- Protocols & reports.
- Internal Quality Audit/ Regulatory Quality Audit Compliance and closure.
- Change control, Standard Operating Procedure, Planned Modification.
- To assist the manager, DGM in batch manufacturingand controlling the functions related of Aerosol department - Manufacturing (MDI, DPI and Nasal Spray).
- Responsible for the day to day production planning of department.
- Work allocation to the operators as per production planning.
- To generate the work order of raw material and packing material as per production planning and to co-ordinate with warehouse department for issuance of materials to achieve schedule plan.
- To informed to quality control department for analysis planning of in process sample as per production schedule and co-ordinate with quality control (QC) department for release of in process and finished product COA.
- To co-ordinate with quality assurance (QA) department for provide the line clearance on time, release of batch, cleaning & process validation.
- To co-ordinate with engineering department for machine maintenance and preventive maintenance schedule.
- Responsible for overall production activities, of the manufacturing area on daily basis in achieving total production requirements in quantity, quality with cGMP requirement.
- Online filling of BMR, BPR of the batches and review of the same.
- Monitor and control the operator for standardize production activity to achieve better productivity and quality.
- Training the men-power to meet the organizational goals and achieve GMP compliance.
- Review, updation & execution of MBMR / MBPR/ SOP /Qualification Protocol whenever is required.
- Responsible for activity related to compliance enhancement programme (CEP) activity as when required.
- Responsible for perform the qualification of new equipment and schedule qualification along with quality engineering (QE) department as when required.
- To adhere with EHS requirement.
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