Organic Chemistry Job Vacancies in Jeedimetla

1. Ensure easy traceability of document/form/SOPs/log books etc issuance and retrieve as per approved written procedures.2. Review and approve procedure and records of raw materials, intermediates, packaging and labelling materials.3. Review and approve completed batch production and laboratory control records before release of saleable intermediates and API for distribution.4. Review and approve of annual product quality review and applicable QMS tracking reports (Change management, deviation management and CAPA management etc.)5. Providing training to cross functional team members on cGMP procedure and revised standard operating procedure, protocols where applicable.6. Handling of QMS documents such as deviations, out of specifications, complaints, returned goods, change controls, incidents, recalls, vendor qualification and CAPA.7. Review & Approve validation protocols and preparations of reports as applicable.8. Ensure that all applicable CAPAs are implemented and effective.9. Approve all specifications and master production instructions.10. Verify the maintenance and calibration data critical equipments as per approved procedure.11. Review and approve stability protocols and reports of API and/or intermediates as applicable12. Delegate applicable QMS activities to immediate sub-ordinates on need basis.13. Participate in self-inspection, other customer/regulatory inspections14. Approve all procedure impacting the quality of intermediate or APIs; production and control operations are clearly specified in written procedure and adopt GMP requirement.15. Approving raw material, intermediate & API contract manufacturer if applicable as per vendor qualification procedure.16. Review and approve of risk assessments reports for product & other risk assessment.17. Review and approve of equipment and other qualification documents.18. Responsible for the vendor auditing (Vendor, Supplier and External labs) preparing report & review and approve of audit co

Qualification: B.Sc (Chemistry) Experience : 0-5 Years1. Charging correct quantities of inputs as per batch manufacturing record.2. Maintain parameters as per batch manufacturing record.3. Following the instructions of shift in charge.4. Ensure safety practice being followed during manufacturing.5. Ensure equipment surroundings cleanness.6. Ensuring the yields and solvent recovery as per yield standards given in the BMR.7. Handle all packaging process stages (packaging and labelling).8. To check the utilities before batch charging.9. To maintain production area in clean & hygiene condition.10. To ensure proper allocation of works to the Helpers.11. To maintain status board and equipment usage log books in on line.12. To maintain the Batch Manufacturing Record (BMR) in on line.13. To ensure proper labeling for in-process sample label, Material status label, Quarantine label and Accessories status label.14. Report any deviations from standards to Shift in-charge Production Manager promptly.

Maintaining Working Area Hygiene Documents, Floor cleaning, Daily calibration recordsas per standard operating Procedure2. Maintaining Proper Labelling System each product.3. Maintaining MSDS (Material Safety Data Sheet) Normal all lab chemicals.4. Maintaining Product Log Books, Patents and R&D Documents.5. Cleaning of the Glassware.6. Maintaining lab chemicals inward documents.7. Following the instructions of shift chemist.8. Before start the work persons should wear Apron, Nose masks, Gloves, Goggles and safetyshoe during process operations.9. Arrange several types of Set-ups in R&D Laboratory.10. To ensure proper allocation of works to the Lab assistant.11. Maintaining online documentation.12. Ensure the all standards; Reagents are within the valid period.

1. Master STP and relevant work sheet and AR review/ revision.2. Analytical Method validation protocol, monitoring and report (9 No's - 2020)3. Investigations of incidents (139 No's - 2020)4. QC SOP revision (Review, Print, signature followup)5. Review of daly, monthly, quarterly and annual calibrations and schedules.6. Organized data backup as per the schedule7. Stablity study initiation as part of CCF/ Add on batch. accordingly protocols to be review and approval8. Review of IM & FP AWS recordsQMS:12. Change control handling (66 No's)13. Deviation Handling14. OOS handling15. Weekly meeting preparation16. MRM preparation17. Audit support.18. CAPA followup19. CAPA effectiveness20. Internal audits followup and closure