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Research Associate - Bioanalytical Operations

Lambda Research Accelerated
Lambda Research accelerated
3-5 years
3,00,000 – 5,00,000
10 Jan. 2, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Research Associate – Bioanalytical Operations

Location: Ahmedabad, Gujarat, India
Employment Type: Full-Time
CTC Range: INR 3,00,000 – 5,00,000 per annum
Experience Required: 3–5 years
Job ID: 1362


Company Overview

Lambda Therapeutic Research Ltd. is a globally recognized, full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With international operations across Mehsana (India), Las Vegas and Pittsburgh (USA), Toronto (Canada), Warsaw (Poland), and London (UK), Lambda delivers integrated clinical research, bioanalytical, and regulatory solutions to innovator, biotech, and generic pharmaceutical companies worldwide.

With a strong foundation in scientific excellence, regulatory compliance, and quality-driven processes, Lambda supports drug development programs across all phases of clinical research.


Role Overview

Lambda Therapeutic Research is seeking a skilled Research Associate – Bioanalytical Operations to join its Bioanalytical team in Ahmedabad. This role is ideal for professionals with hands-on experience in bioanalytical method development and validation, particularly within regulated laboratory environments. The position offers exposure to advanced analytical platforms and global clinical research projects.


Key Responsibilities

  • Develop, validate, and document bioanalytical methods in compliance with regulatory standards.

  • Perform sample processing and analysis for assigned bioanalytical studies.

  • Operate, calibrate, and troubleshoot LC–MS/MS systems and associated analytical instruments.

  • Prepare and review draft analytical methods, method-specific SOPs, and study documentation.

  • Ensure strict adherence to system-, method-, and study-specific SOPs, protocols, and plans.

  • Maintain compliance with GLP, OECD GLP principles, and 21 CFR Part 11 requirements.

  • Verify instrument labeling, calibration status, and completeness of equipment logbooks.

  • Ensure all required training is completed prior to initiating bioanalytical activities.


Experience & Skills

  • 3–5 years of relevant experience in bioanalytical method development, validation, and sample analysis.

  • Hands-on expertise with LC–MS/MS instrumentation and bioanalytical workflows.

  • Strong understanding of GLP regulations, OECD GLP principles, and 21 CFR Part 11 compliance.

  • Ability to work accurately within regulated laboratory environments with strong attention to detail.

  • Good documentation practices and effective written and verbal communication skills.


Educational Qualifications

  • M.Pharm, M.Sc., or B.Pharm in Pharmaceutical Sciences, Analytical Chemistry, or a related discipline.


Why Join Lambda Therapeutic Research?

  • Work with a globally established CRO supporting diverse clinical and bioanalytical programs.

  • Exposure to international regulatory standards and advanced analytical technologies.

  • Competitive compensation aligned with skills and experience.

  • Opportunity to grow professionally in a quality-driven and collaborative research environment.


Apply Now
Take the next step in your bioanalytical research career with Lambda Therapeutic Research Ltd. and contribute to high-impact global drug development programs.