Pharma Jobs in Ahmedabad: Lambda is Hiring |
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Are you currently looking for Pharma Jobs in Ahmedabad? Lambda Therapeutic Research Ltd., a leading Global Clinical Research Organization (CRO), is hiring a Research Associate in Bioanalytical Operations at its Ahmedabad facility. This opportunity offers professionals with 2–3 years of experience in bioanalysis, method validation, and LC-MS/MS operations a chance to work in a world-class research environment that adheres to GLP and 21 CFR Part 11 compliance standards. Apply Now for Research Associate Jobs and kickstart your career.
Job Details:
- Job Title: Research Associate – Bioanalytical Operations
- Req ID: 1363
- Location: Ahmedabad, India
About the Company:
Lambda Therapeutic Research Ltd. is a leading Global Clinical Research Organization (CRO) headquartered in Ahmedabad, India, delivering high-quality, end-to-end clinical research services to the global pharmaceutical, biotech, and generic drug industries. With a strong international presence across India, the USA, Canada, Poland, and the UK, Lambda offers a full spectrum of clinical development solutions — from bioanalytical and bioequivalence studies to clinical trials and regulatory support. Driven by scientific excellence, compliance, and innovation, Lambda adheres to OECD GLP, 21 CFR Part 11, and other international quality standards. The organization’s commitment to operational excellence and ethical research practices makes it a trusted partner for global pharmaceutical advancements.
Educational Qualification:
M.Pharm / M.Sc. / B.Pharm
Key Responsibilities for the Research Associate:
- Develop and validate bioanalytical methods.
- Process and analyze samples for allotted projects.
- Operate, calibrate, and troubleshoot LC-MS/MS instruments and other analytical devices.
- Prepare draft and method SOPs; ensure compliance with System/Method Specific SOPs and relevant Plan/Protocol.
- Ensure training for all required SOPs/documents before initiating any related activities.
- Implement Good Laboratory Practices (GLP) and 21 CFR Part 11 by maintaining equipment logbooks, verifying instrument labels, and ensuring timely calibrations.
- Work according to OECD GLP principles to maintain the highest standards of research integrity.
Experience Required for the Research Associate:
2–3 years in bioanalytical method development and LC-MS/MS operations.
