- Carrying out method development, validation, and study sample analysis according to Good Laboratory Practices (GLP), in-house SOPs, and working instructions.
- Ensuring compliance with GLP guidelines for managing the laboratory, including safety, security, and maintenance of equipment.
- Monitoring laboratory work involving various processing techniques, analytical methods, and standard operating procedures in compliance with GLP and approved protocols.
- Reviewing raw data and chromatographic data, and continuously updating the status of ongoing studies to the investigator/manager.
- Reviewing Method SOPs and bio-analytical reports of method validation and studies.
- Performing specific tasks like MD/MV and study sample analysis according to SOPs and working instructions of various equipment and maintaining related records.
- Retrieving plasma, bulk spiking, processing samples along with CC, QC’s according to method SOP and written procedures.
- Ensuring cleanliness of the laboratory and proper disposal of non-bio-waste & bio-waste.
- Preparing bio-analytical reports, SOPs, and Method SOPs.
Qualifications:
- M.Pharm/B.Pharm/M.Sc in Life Sciences
Interview Dates:
- 8 July 2024 to 12 July 2024
- 09:30 AM to 12:30 PM every day
Venue:
- Axis Clinicals Limited, 1-121/1, Survey Nos.66 (Part) & 67(Part), Gachibowli – Miyapur Rd, Serilingampalle (M), Telangana
Contact Information:
- For more information, please contact: Sampathkumar.p@axisclinicals.com