6 Jobs in Palasbari

Responsible for Receipt of Raw, Packing and Miscellaneous Materials as per cGMP norms. Responsible for all time readiness for inspections by continuous monitoring of cGMP and regulatory norms. Responsible and ensure online documentation related to warehouse. Responsible for indenting of miscellaneous materials as per requirement and follow ups with purchase for delivery Responsible for arrangement, storage, issuance and reconciliation of Miscellaneous / consumable materials Responsible for arrangement of materials & cleaned accessories for dispensing Responsible for area cleanliness and monitoring of Temperature and RH of storage area as per SOP Responsible for Packing materials releases from QC as per requirement Responsible for arrangement of packing materials for dispensing Responsible for dispensing of Packing materials as per SOP. Responsible for handling of MRN (Return material) and its verification and putway on warehouse bin. Responsible for handling of Online rejection and rejected materials and its disposal. Responsible for staking the material as per respective location and same shall be updated in system by using RF gun. Responsible for Verification and calibration of weighing balances Responsible for tracking of freight bills and transfer to SSC department. To ensure all the material storage conditions are maintained as per the prescribed limit. Responsible for physical stock checking of RM/PM as per SOP. To ensure all the instruments or equipments of warehouse shall be in operation condition as per SOP. Responsible for follow EHS norms as per safety policy. Any other responsibility assigned by immediate superior or head of department. Job Location :Palasbari, Guwahati Assam

Responsible for warehouse function of Raw material, Packing material, Finished goods and Miscellaneous stores activities with respect to statutory and regulatory /compliance cGMP. To co-ordinate with internal customer (I.e production, engineering, QA, QC, Tech transfer ,EHS, Central purchase, Logistic HR, Admin) and factory management in routine for smooth operation. To ensure Receipt of Raw and Packing material as per SOP. To ensure dispatch of finished goods as per market requirement with co-ordination of SCM & distribution team. To ensure all time readiness for inspections by continuous monitoring of cGMP & Regulatory norms. To ensure online documentation related to warehouse. To ensure implementation of warehouse system as per cGMP & SOP training to employees for better control to systemize the function in warehouse. Ensure that, the proper review of deviation, change request documentation, risk assessment and CAPA in consultation with responsible person involved in the activity and quality assurance. To ensure dispensing of RM & PM as per SOP. To ensure all the material storage conditions are maintained as per the prescribed limit. To ensure Temperature Sensitive materials shall be received as per SOP along with availability of transit temperature data. Clearance of Rejected & Expired inventory with support of QC & purchase team. To ensure & responsible for physical inventory of RM/PM as per SOP. To ensure packing materials availability with support of purchase team as per packing requirement. To ensure area cleanliness of warehouse as per SOP. To ensure all the instruments or equipments of warehouse shall be in operation condition as per SOP. To ensure PR of RM & PM as per requirement /roller forecast. To maintain Inventory of RM, PM & consumable items as per production requirement / forecast. To review Inventory data on monthly basis & take action plan on near expiry, Non-moving inventory with co-ordination with production, SCM & purchase team. To ensure preparation of MDNs of Obsoleted, Rejected & Expired materials & destroy it after approval in MDN flow as per SOP. To ensure proper control & maintain record of psychotropic substances from receipt to FG dispatch. To ensure quarterly return submitted to NDPS department of psychotropic substances. To ensure monthly return submission of Alcohol to government authority. To ensure dedicated storage of recall / rejected goods. To ensure proper maintain of Engg. Stores. To ensure daily scrap vehicle removal from plant to approved vendors. Responsible for follow EHS norms as per safety policy, Ensure the safety in stores department with respect to man, material, equipment and facility during the work. Ensure the adequate manpower availability in the department ,training to the new recruited staff and time to time support and guidance to perform work smoothly. Admistratively responsible for scheduling of employee work disciplinary matter, identification their training need, Conductory training for person, one helping them progress in their carrier development. Any other assignment allocated by department head Job Location: Palasbari, Guwahati Assam

1. Planning and preparation of qualification protocols and documents for equipment, instruments, systems, including of utilities, manufacturing process, packing equipment. 2. Review, execution and compilation of qualification protocols and documents for equipment, instruments, systems, including of utilities, manufacturing process, packing equipment. 3. Preparation of yearly and add-on schedule for Periodic Performance Verification-Performance Testing (PPV-PTS). 4. Preparation of yearly and add-on schedule for Periodic Performance Verification-Support Programme Review (PPV-SPR). 5. Follow and ensure compliance of validation SOPs, policy documents and written procedures. 6. Follow and ensure the current Good Manufacturing Practices as per applicable SOPs. 7. Provide training to the personnel involved in qualification and validation activities as & when required. 8. Arrangement, Tracking, Preparation, Review & compliance for the document required for Inspection at site. 9. Co-ordination with CFT for smooth functioning of qualification activity. 10. Any other responsibility that may be assigned by HOD or reporting manager from time to time. Secondary Responsibility 11. Participation in quality improvement projects. 12. Extend need based support to DF Sites, viz. Sun Pharmaceutical Industries Limited (SPIL), India sites and Overseas DF locations. 13. Any other responsibility that may be assigned by HOD or reporting manager from time to time. Interested candidates can send resumes to akash.gogoi@sunpharma.com Job Location: Palashabri, Assam, Guwahati Contact No: 8473959757

1. Responsible for the Handling of market complaint at site. 2. Responsible for the Handling of Deviation management at site. 3.Responsible for the Handling of CAPA and Global CAPA management and effectiveness checking at site. 4.Responsible to co-ordinate the execution of mock recall and market recall. 5.Responsible to review and tracking of Audit Responses. 6.Responsible to raise, review and tracking of Quality Alert. 7.Responsible to ensure timely closure of QMS documents. 8.To perform activity as per authorization in EDMS, LMS and TRACKWISE software. 9.Responsible for performing IPQA activities. 10.To perform process validation and cleaning validation sampling activity in shop floor. 11.To review new/exhibit/transfer and executed master BMRs and BPRs. 12.To review batch records and associate annexures, checklists etc. 13.To perform Product/Recipe approval, SFG/FG release, sampling, sample posting etc. in SAP HANA systems 14.To prepare and execute hold time study protocol and perform sampling activity. 15.To prepare and review process validation protocol and report. 16.Preparation and Review of Annual product quality review. Interested candidates can send resumes to akash.gogoi@sunpharma.com Job Location: Palashbari, Mirza, Assam Contact No: 8473959757

1. To maintain and ensure cGMP/cGLP in the Quality Control Department. 2. To maintain documents as per GLP requirements. 3. To perform the activity as per work allotment. 4. To follow the SOP/ATP/STP and protocols. 5. To maintain the laboratory neat and clean. 6. To perform sampling and analysis of Packing material sample and maintain online documentation. 7. To maintain the data integrity and to plan the work such as to give maximum productivity within stipulated time. 8. To perform daily monitoring of temperature. 9. To participate with supervisor to close the investigation for deviation, Incidents, OOT and OOS. 10. To follow safety procedure in the laboratory. 11. To report the result of analysis carried out by contract laboratory. 12. To perform all operation in QC lab carried out as per the written procedure. 13. Handling of LIMS software and LMS software etc. Secondary responsibility: 1. To perform analysis of Raw material,FP,PV/AMT sample and Stability Sample and maintain online documentation as and when required. 2. To perform the daily verification of instrument as and when required. 3. Any other additional work allocated by reporting authority. Interested candidates can send resumes to akash.gogoi@sunpharma.com Job Location: Palashbari, Mirza, Assam Contact No: 8473959757

1. He is authorized to sign (as a Doer/Checker) Parenteral GMP documents, Batch Manufacturing record Process validation Record Daily observation compliance Qualification document Execution of aseptic process simulation (Media Fill) Department SOPs (EDMS) and study protocol Assign to person in CAPA, Initiator and lead investigator in incident and investigation. 2. He can Perform and ensure the equipment cleaning and usage log, Start-up activities and line clearance, Documentation practices, labelling practices throughout operation. 3. Preparation or assist of various protocol and reports, as required in execution of process validation, cleaning validation/verification and characterization batches. 4. The supervisor is responsible for production activities of clean area day to day basis in achieving total production requirements in quality, quantity and GMP compliance in preparation area. 5. Preparation and reviewing of process related logbooks, SOP(s), BMR and other relevant documents. 6. Daily recording of RH, Temperature and differential pressure of area and equipment as per requirement. 7. Working as per instruction provided by Senior to achieve the daily production plan. 8. Co-ordination with engineering department for preventive maintenance schedule. 9. Participate relevant training prior to perform any activity. 10. To follow aseptic behaviour in side aseptic area. 11. Generate requirement for Consumable Items and other miscellaneous items (SAP) required for smooth production operation. 12. Responsible for maintenance and inventory control, safe keeping and availability of change over parts and spare part. 13. Involving in planning, execution as per planning and allocation/managing of manpower. 14. Responsible for Manufacturing area and all production related activity in parenteral department. 15. Handling of additional activities/task allotted by HOD. Interested candidates can send resumes to akash.gogoi@sunpharma.com Job Location: Palashbari, Mirza. Assam Contact No: 8473959757