NOTE: Only Male & Candidates from AP & Telangana Preferred.Kindly Understand the JD & PCI Mandatory 3-Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Kindly carry your educational documents set #MANDATORY 1. Study Custodian Requirements: B.Pharm + PCI Key Responsibilities: Oversee study-related documentation and ensure compliance with regulatory standards. 2. Pharmacist Requirements: B.Pharm + PCI Key Responsibilities: Manage medication dispensing, ensure patient safety, and collaborate with clinical teams. 3. ARA (Assistant Research Associate) Requirements: DMLT + B.Sc Key Responsibilities: Support clinical trials, collect and analyze lab samples, and assist in data collection. 4. Staff Nurse Requirements: Registered Staff Nurse (B.sc Nursing) Key Responsibilities: Provide direct patient care, support clinical trial procedures, and ensure patient safety. Location: Axis Clinicals Limited, Miyapur, HYD. Interested can Directly Walkin on Saturday,5th April 2025 from 10am to 12pm along with your Resume & certifixcates

NOTE: Only Male & Candidates from AP & Telangana Preferred.Kindly Understand the JD It's not for the Clinical Trails Department 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period.Qualifications required: Bachelors / Masters (0-4 yrs. experience) degree level in biological/ life science, pharmacy qualification.Role and responsibility:In process quality control of ongoing studies.Review of raw data, chromatograms and reports of the method validations and studies.Checking of all the instruments and equipments for the calibration status and appropriate labeling.Checking and monitoring of the day-to-day activities in the lab for compliance to SOPs and GLP principles.Checking of the concentration data of subject samples before releasing to PK department.Generation, control and distribution of method SOPs.Logbook handling and archival of the completed logbooks.Performing the routine glassware validations and monitoring of the temperature and humidity in the Bio-analytical lab.Calibration of pipettes and multipedes.Coordinating for training programs on SOPs.Ensure cleanliness of laboratory and disposal of non-bio-waste & Bio-waste.

Qualifications required: Bachelors /Masters (2-5 Years of experience in Bioanalytical Department Role and responsibility:1. To work on the method development / validation / study sample analysis using HPLC, LC/MS/MS techniques as per principles of GLP, SOPs and approved protocols.2. To plan and monitor the laboratory work involving the various processing techniques, analytical methods and standard operating procedures (SOPs) and complying with the principles of Good Laboratory Practices (GLP) as well as approved protocols to ensure the quality, integrity and reliability of the results.3. To establish quality control program and safety of the staff and to establish corresponding corrective actions.4. To review the raw data forms and chromatographic data sheets5. To electronically transfer the data duly checked with the raw data and chromatograms to Pharmacokinetics department for PK analysis.6. Review of Method SOPs, bio-analytical reports of Method Validation and Studies.7. Review and/or approval of operational SOPS and Method SOPs.8. Training of personnel.9. Responding to queries from Sponsor and/or regulatory authorities.