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2-3 years
4 to 5 Lacs
10 June 12, 2025
Job Description
Job Type: Full Time Education: B.Pharm/M.Pharm/M.Sc 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 Scientist – Bioanalytical Operations | Lambda Therapeutic Research Ltd. | Ahmedabad, India
Req ID: 1202
Department: Bioanalytical Operations
Date Posted: June 5, 2025
CTC Range: ₹4,00,000 – ₹5,00,000 per annum


Company Overview:
Lambda Therapeutic Research Ltd. is a leading full-service Global Clinical Research Organization (CRO), headquartered in Ahmedabad, India. With global operations in the USA, Canada, UK, Spain, and Poland, Lambda is a trusted partner for end-to-end clinical research services in the innovator, biotech, and generic pharmaceutical sectors.


Position Summary:
Lambda is seeking a Research Scientist for its Bioanalytical Operations team at the Ahmedabad site. The ideal candidate will contribute to bioanalytical method development, validation, and regulated sample analysis, while ensuring adherence to industry compliance standards including GLP and 21 CFR Part 11.


Key Responsibilities:

  • Develop and validate bioanalytical methods in line with global regulatory guidelines.

  • Perform bioanalytical sample processing and analysis for assigned studies.

  • Operate, calibrate, and troubleshoot LC-MS/MS systems and other lab instrumentation.

  • Draft and maintain method-specific SOPs, ensuring alignment with study plans and protocols.

  • Undergo mandatory training on all applicable SOPs prior to initiating any project-related tasks.

  • Implement GLP and 21 CFR Part 11 standards by:

    • Verifying calibration due dates of instruments.

    • Ensuring completeness of logbooks.

    • Monitoring instrument usage labels and documentation.

  • Comply with OECD GLP principles throughout operations and reporting.


Qualifications:

  • M.Pharm / B.Pharm / M.Sc. in a relevant scientific field

  • 2–3 years of hands-on experience in bioanalytical method development and LC-MS/MS instrumentation

  • Strong understanding of GLP, regulatory documentation, and quality assurance practices


Key Competencies:

  • High accountability and attention to detail

  • Clear written and verbal communication skills

  • Strong work ethic and time management

  • Effective presentation and documentation abilities

  • Strong cultural fit and ability to work in a cross-functional team


Salary: ₹4,00,000 – ₹5,00,000 per annum