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Research Associate - Bioanalytical Operations

4 to 5 Lacs years
2-3
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 Associate – Bioanalytical Operations | Lambda Therapeutic Research Ltd. | Ahmedabad, India
Req ID: 1214
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 international operations in the U.S., Canada, U.K., Spain, and Poland, Lambda offers comprehensive clinical research services for innovator, biotech, and generic pharmaceutical clients.


Position Summary:
We are hiring a Research Associate in our Bioanalytical Operations department in Ahmedabad. This role involves bioanalytical method development, validation, and sample processing using advanced instrumentation, with strict adherence to GLP and regulatory standards.


Key Responsibilities:

  • Develop and validate robust bioanalytical methods in compliance with regulatory guidelines.

  • Process and analyze biological samples for allocated research projects.

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

  • Prepare draft and method-specific SOPs; ensure compliance with all SOPs and relevant protocols.

  • Conduct mandatory training on all applicable SOPs/documents before initiating related activities.

  • Ensure adherence to GLP standards and 21 CFR Part 11 regulations, including:

    • Monitoring instrument calibration due dates.

    • Verifying instrument labels and logbook accuracy.

    • Maintaining audit-readiness across lab operations.

  • Perform tasks aligned with OECD GLP principles and maintain high standards of documentation and traceability.


Qualifications:

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

  • 2–3 years of experience in bioanalytical research, preferably in a regulated CRO environment

  • Hands-on experience with LC-MS/MS instrumentation and troubleshooting

  • Solid understanding of GLP, regulatory protocols, and documentation standards


Key Competencies:

  • Accountability and proactive attitude

  • Effective communication (written and verbal)

  • Strong work ethic and consistent performance

  • Initiative-driven and solutions-oriented mindset

  • Presentation and technical reporting skills

  • Cultural alignment with organizational values


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