Research Associate Jobs at Lambda Therapeutic | MSc Chemistry Jobs
Lambda Therapeutic Research is hiring Research Associates for its Bioanalytical Operations team in Ahmedabad. This role is ideal for candidates with hands-on experience in LC-MS/MS, bioanalytical method development, and GLP-compliant workflows. If you’re looking to grow your career in clinical research and bioanalysis, this opportunity lets you work on global projects in a top CRO environment. Interested candidates are invited to apply for the exciting opportunity of MSc Chemistry Jobs at Lambda Therapeutics.
Company Overview
Lambda Therapeutic Research Ltd. 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 Title: Research Associate – Bioanalytical Operations
- Req ID: 1363
- Date: Nov 15, 2025
- Location: Ahmedabad, India
- Company: Lambda Therapeutic Research Ltd.
- CTC Range (INR): 300000 – 500000
Organizational 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)
Job Description:
- To develop and validate Bioanalytical methods.
- To process / analyze samples of allotted projects.
- To operate, calibrate and troubleshoot 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.
Experience: 2 to 3 years
Educational Qualification:Â M.Pharm/M.Sc./B.Pharm
