To prepare and issue SOPs. BMR / BPR verification. Verification of Rejected Material in Stores. To check calibration status of production instruments/ equipments periodically. To perform the in process analysis. Required Candidate profile To give line clearance during product change over. To supervise the dispensing of raw materials. To organize and collect the ln process, intermediate and Finished Product samples during Manufacturing.

To Operate and clean tube/tin filling and packing machine, Shrink machine, Aggregation Machine, Domino Printing machine, Leak Test Apparatus, Literature folding machine. Operation and cleaning of Autoclave

1. Preparation of Annual/Periodic Product Quality Review (APQR/PQR) 2. Preparation of finished product specification (Tablet, External preparations & Injection) 3. Preparation of Protocol and Reports of PROCESS VALIDATION Batches. 4. Handling of Incidents, Deviation, CCP, OOS, OOT and Material Rejections 5. Issuing BARCODES for new Registered products in coordination with regulatory department. 6. Working Hands on MARKET COMPLAINTS and CAPA. 7. Preparation of Master Formula Record (MFR) and Preparation Of (SOPs). 8. Preparation of EQUIPMENT QUALIFICATION documents i.e. IQ, OQ, PQ protocol and Reports during Installation of New Instruments/ Equipments. 9. Identification of Hazard and Calculation of Risk associated with product or daily activity. 10 Participation and Handling of SELF INSPECTION Reports (INTERNAL AUDIT). 11. Preparation of Audit & Maintenance of Post Audit Documents (compliance reports). Desired Candidate Profile Bachelor's degree in Science (B.Sc) or Pharmacy (B.Pharma). Male candidate will be preferred.

1) Prepare and review new as well as Re-registration CTD and ACTD dossiers and handling queries for all Formulations 2) All FDA related applications and follow ups through Xln india, FDA-WHO GMP sites including Import permissions, Export NOC, and new FDC applications through CDSCO-Sugam Portal. 3) Co-ordinate with Quality Assurance dept. for preparation of documents which is required for FDA purpose (Inspections) as well as any registration process (Export countries regulatory agencies audits) 4) Responsible for preparing and biding local as well as export tenders 5) Trademark and Copyright registration records to be tracked and updated.

1. To prepare & review SOP, BPR, BMR, Protocol 2. To plan production schedule effectively as per export order & market requirement. Also, availability of RM/PM. 3. To co-ordinate with various production dept to achieve the goal laid down by the mgt. Required Candidate profile 4. To follow good housekeeping program & maintain proper cleaning of the dept as per CGMP. 5. To give job training to subordinates & workmen. 6. Reconciliation after completion of batch activity.

1. To prepare & review SOP, BPR, BMR, Protocol. 2. To plan production schedule effectively as per export order & market requirement as per availability of RM/PM. 3. To co-ordinate with cross functional dept to achieve the goal laid down by the mgt. 4. To follow good housekeeping program & maintain proper cleaning of the dept as per cGMP. 5. To give job training to subordinates & workmen. 6. To ensure proper safety, maintenance of machinery & equipment of the dept. 7. To ensure various in-process control checks during the production of the batch as given in BMR & BPR. 8. To do reconciliation after completion of batch activity. 9. To ensure appropriate process validation, equipment qualification & calibration. 10. To identify and report operational as well as maintenance problems to avoid production delay. 11. To have effective control on manpower and machine utilization on daily basis. 12. To guide officers or workers in case of any technical problems or issues. 13. To provide technical input/suggestions towards new product development/improvement in process. 14. To ensure online documentation of BMR, BPR, logbooks, validation, protocols, reports of all production activities. 15. To prepare and send daily production report to the plant head/management. 16. To sent intimation of indent of raw material, packing material. 17. To transfer the finished goods to FG store Dept. 18. To perform various trial batches as per requirements. 19. To co-ordinate with workers, officers, plant head/management for smooth conduct of audit. Perks and benefits

1. Preparation of Annual/Periodic Product Quality Review (APQR/PQR) 2. Preparation of finished product specification (Tablet, External preparations & Injection) 3. Preparation of Protocol and Reports of PROCESS VALIDATION Batches. Required Candidate profile 4. Handling of Incidents, Deviation, CCP, OOS, OOT and Material Rejections 5. Issuing BARCODES for new Registered products in coordination with regulatory 6. MARKET COMPLAINTS and CAPA.