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.”
Responsibilities:
- To ensure contamination control are available and followed at site as per Contamination Control Strategy (CCS) and respective procedures.
- Handling of QMS activities (OOT / OOS / Market complaint / Investigation / CAPA / deviation & change control).
- Implementation of site and global CAPA w.r.t. Block-P.
- To prepare audit (Self Inspection/Customer/External Inspection/Regulatory) observation response.
- To review & approve all the documents related to validation like protocols/reports etc.
- To explain the process and documents to auditors during the audits and implement the recommendation of internal/external/regulatory audits outcome and ensure audit compliance.
- To review & approve the SOPs, specifications, packing instruction relating to production & ensures their implementation.
- To ensure timely completion of validation/qualification activities for aseptic process simulation (Media Fill), equipment’s & systems as per approved procedure.
- To plan the packing activities of the department as per weekly / monthly delivery schedule.
- To meet the production schedule both in quantity & quality.
- To ensure the hygiene & maintenance of packing department, system & equipment are in neat & tidy condition at all time.
- To do counselling & grievance handling of the subordinates of packing section.
- To ensure that the finished products are produced & stored according to appropriate documentation & meet timely deliveries as per production schedule.
- To review the Batch Production Record / POPI & FOMI.
- To ensure completion of SAP Transaction on time.
- To review & approve for Master Batch Packing/Manufacturing Record.
- To perform in process checks & record in log books & PI / MI.
- Issuance of material from block store to process area as per P.O. / F.O and updates the stocks in SAP.
- To ensure online recording data and complete the documentation on time.
- To support the manufacturing section as and when required.
- Any other responsibility / task given by management/HOD from time to time.
- To maintain Harmony relationship with peers, seniors at work place and ensure the win - win situation for resolution of issues.
- Ensuring adherence to GMP, EHS standards, and SOPs across Block P through continuous monitoring.
- Responsible for maintaining departmental hygiene.
- To ensure that products are produced and stored in accordance with the appropriate documentation in order to obtain the required quality and monitoring of storage conditions for materials / products.
- To monitor and ensure strict implementation of all in process controls.
- To ensure that the production records are evaluated and signed by a designated person.
- To ensure proper maintenance of the department, premises, and equipment, as well as monitoring & controlling the manufacturing environment.
- To ensure that all required process validations, equipment calibrations are performed and that the corresponding reports are available
- To ensure that the required initial / continuing training of production personnel is carried out and adapted according to need.
- To ensure that documentation is maintained in accordance with the defined retention period
- To ensure that suppliers of materials are properly approved and regularly monitored.
