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Hiring Research Associate – GLP Compliance | Lambda Therapeutic Research Job

Published on

Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

Lambda Therapeutic Research is a leading Global Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With facilities in Mehsana (India), Las Vegas (USA), Pittsburgh (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), Lambda provides end-to-end clinical research services to pharmaceutical, biotech, and generic drug companies worldwide. The company is known for its GLP-compliant, OECD-aligned, and 21 CFR Part 11-regulated bioanalytical research.

Job Description: Research Associate – Bioanalytical Operations

As a Research Associate in Bioanalytical Operations, you will be responsible for:

✔ Developing and validating bioanalytical methods (LC-MS/MS)
✔ Processing and analyzing samples for assigned projects
✔ Operating, calibrating, and troubleshooting LC-MS/MS and other analytical instruments
✔ Preparing draft methods, SOPs, and ensuring compliance with GLP, OECD, and 21 CFR Part 11 guidelines
✔ Ensuring instrument calibration and maintaining logbooks
✔ Training on SOPs before initiating any project-related activities

Key Competencies Required

✅ Strong communication and presentation skills
✅ High work ethic and accountability
✅ Ability to fit into organizational culture
✅ Knowledge of GLP, OECD, and regulatory compliance

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Eligibility Criteria

  • Education: M.Pharm / B.Pharm / M.Sc (Life Sciences)
  • Experience: 2-3 years in bioanalytical method development (LC-MS/MS)
  • Location: Ahmedabad, Gujarat

How to Apply?

Application Link