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Research Associate | Lambda Therapeutic Research Ltd

Lambda Research accelerated
2-3 years
₹4.0 – ₹5.0 LPA
Ahmedabad, India
15 July 20, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Research Associate | Lambda Therapeutic Research Ltd.

Job Details

  • Job Title: Research Associate

  • Company: Lambda Therapeutic Research Ltd.

  • Job ID (Req ID): 1213

  • Department: Bioanalytical Operations

  • Location: Ahmedabad, Gujarat, India

  • Job Type: Full-time

  • Experience Required: 2–3 years

  • Educational Qualification: M.Pharm, B.Pharm, or M.Sc.

  • CTC Range: ₹4.0 – ₹5.0 LPA

  • Posted Date: 16 July 2026


About the Company

Lambda Therapeutic Research Ltd. is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operations across India, the USA, Canada, Poland, and the UK, the company provides comprehensive clinical research services to innovator, biotechnology, and generic pharmaceutical companies worldwide.


Job Purpose

The Research Associate will be responsible for bioanalytical method development, validation, sample analysis, and operation of LC-MS/MS instruments while ensuring compliance with GLP, OECD GLP, and 21 CFR Part 11 guidelines.


Key Responsibilities

  • Develop and validate bioanalytical methods for research studies.

  • Process and analyze biological samples for assigned projects.

  • Operate, calibrate, and troubleshoot LC-MS/MS and other analytical instruments.

  • Prepare draft methods and Standard Operating Procedures (SOPs).

  • Ensure compliance with system-specific and method-specific SOPs.

  • Complete all required training before performing project-related activities.

  • Ensure effective implementation of GLP, OECD GLP, and 21 CFR Part 11 requirements.

  • Verify equipment labels, instrument logbooks, and calibration records.

  • Ensure instruments are calibrated before their due dates.

  • Maintain accurate documentation and adhere to quality standards.


Required Qualifications

  • M.Pharm, B.Pharm, or M.Sc.

  • 2–3 years of experience in Bioanalytical Operations or a related pharmaceutical/CRO laboratory.

  • Knowledge of LC-MS/MS instrumentation and bioanalytical techniques.

  • Understanding of GLP, OECD GLP, and 21 CFR Part 11 guidelines.


Preferred Skills

  • Bioanalytical method development and validation.

  • LC-MS/MS operation and troubleshooting.

  • Sample preparation and analysis.

  • Analytical instrumentation handling.

  • GLP and OECD GLP compliance.

  • 21 CFR Part 11 knowledge.

  • SOP preparation and documentation.

  • Quality assurance and regulatory compliance.

  • Data analysis and reporting.

  • Laboratory safety and good documentation practices.


Core Competencies

  • Accountability.

  • Effective communication.

  • Strong work ethic.

  • Presentation and communication skills.

  • Teamwork and organizational culture fit.


One-Line Experience

Candidates with 2–3 years of experience in bioanalytical laboratories, LC-MS/MS analysis, method development, and GLP-compliant pharmaceutical or CRO environments are preferred.


Salary Package

  • Official CTC: ₹4.0 – ₹5.0 LPA

  • Market Standard: ₹4.5 – ₹6.5 LPA (depending on LC-MS/MS expertise, bioanalytical experience, and CRO/pharmaceutical background).


Why Join Lambda Therapeutic Research?

  • Opportunity to work with a globally recognized Clinical Research Organization (CRO).

  • Hands-on experience in bioanalytical research using advanced LC-MS/MS technology.

  • Exposure to global clinical research projects and regulatory standards.

  • Strong learning environment with career growth opportunities in bioanalysis and clinical research.

  • Competitive compensation and professional development opportunities.