Research Scientist

Lambda Therapeutic Research Ltd.; India; On-site; INR 350,000 - 550,000; Full time

Job summary

Lambda Therapeutic Research Ltd. in Ahmedabad, Gujarat, invites applications for a Research Associate in Bioanalytical Operations.

The role focuses on developing and validating bioanalytical methods and handling sample analysis for various projects. You will operate and troubleshoot LC-MS/MS and other analytical instruments, prepare SOP drafts, and ensure GLP and 21 CFR Part 11 compliance, with emphasis on proper logbooks and equipment calibration.

Responsibilities

• To develop and validate Bioanalytical methods.
• To process /analyze samples of allotted projects.
• To operate, calibrate and troubleshooting of LC-MS/MS instruments and other analytical instruments.
• Preparation of draft and method SOP and to work in-compliance to System/Method Specific SOPs and relevant Plan/Protocol.
• To ensure training of all required SOPs/documents prior to initiating any related activities.
• To ensure effective implementation of GLP and 21CFR Part 11 by checking of instrument labels, completeness of logbooks of equipment’s and instruments and ensuring the instrument calibrations are done before due date. Work as per OECD GLP principles.

Skills

Bioanalytical methods

LC-MS/MS operation

GLP compliance

Tools

LC-MS/MS instruments

Job description

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Company: Lambda Therapeutic Research Ltd.

CTC Range (INR): 350000 - 550000

ORGANISATIONAL OVERVIEW

Lambda Therapeutic Research is a full-service Global Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Pittsburgh (USA), Toronto (Canada), Warsaw (Poland) and London (UK), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries.

JOB DETAILS

Department: Bioanalytical Operations

Designation: Research Associate

Job Location: Ahmedabad (Gujarat)

KEY DELIVERABLES

• To develop and validate Bioanalytical methods.
• To process /analyze samples of allotted projects.
• To operate, calibrate and troubleshooting of LC-MS/MS instruments and other analytical instruments.
• Preparation of draft and method SOP and to work in-compliance to System/Method Specific SOPs and relevant Plan/Protocol.
• To ensure training of all required SOPs/documents prior to initiating any related activities.
• To ensure effective implementation of GLP and 21CFR Part 11 by checking of instrument labels, completeness of logbooks of equipment’s and instruments and ensuring the instrument calibrations are done before due date. Work as per OECD GLP principles.