Research Associate

Cadila Pharmaceuticals

  • Dholka, Gujarat
  • Permanent
  • Full-time
  • 1 month ago
Core responsibility related to GLP: 1. Record raw data accurately and directly during conduct of activity, verify the data collected, prepare reports and archive these records 2. Request for test and reference item and its receipt, safe handling and disposal as per in-house SOPs 3. Participate in method development and method validation studies of various molecules 4. Preparation and labelling of reagents, solutions chemicals and testing samples in the laboratory areas 5. Wearing appropriate protective clothing and follow all safety precautions 6. Operation, calibration, cleaning, labelling and maintenance of instruments used for routine activity and maintain these records 7. Maintaining cleanliness of the section. 8. Procurements of materials for conduct of experimental activity in laboratory. 9. Request for controlled documents and maintain accountability as per in-house SOPs 10. Participate in the formulation sample analysis as per in-house SOP and study plan 11. Coordinating with RQA during the facility audits and study based inspections and complying with RQA audit observations 12. Ensure computerized system used in study is validated 13. Prepare and follow STPs for the samples analysis according to analytical method development & validation 14. Preparation of SOPs relevant to activities performed in laboratory area, conduct the training on SOPs Allied responsibility: 15. General material procurement. 16. Following GPCB guidelines for waste management system and maintenance of its records 17. Performing assigned duties on weekly off and holidays based on requirements, where required. Any additional responsibility / activity as and when assigned by management which would not arise any conflict of interest.

Cadila Pharmaceuticals

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