Job Title: Research Associate – Bioanalytical Operations
Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, Gujarat, India
Job ID: 1213
Employment Type: Full-Time
Experience Required: 2–3 years
CTC Range: INR 4,00,000 – 5,00,000 per annum
About the Company
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The company operates advanced clinical research facilities across Mehsana (India), Las Vegas (USA), Pittsburgh (USA), Toronto (Canada), Warsaw (Poland), and London (UK).
Lambda provides comprehensive end-to-end clinical research solutions to global pharmaceutical innovators, biotechnology companies, and generic drug manufacturers. With strong expertise in bioanalytical research, regulatory compliance, and clinical development, the organization supports high-quality clinical trials and laboratory services worldwide.
Job Overview
Lambda Therapeutic Research Ltd. is seeking a skilled Research Associate to join the Bioanalytical Operations team in Ahmedabad. The role involves developing and validating bioanalytical methods, performing sample analysis, and ensuring laboratory compliance with GLP standards and regulatory guidelines.
The ideal candidate will have experience working with LC-MS/MS instruments, strong analytical capabilities, and a thorough understanding of laboratory quality systems. This role offers an opportunity to contribute to high-impact clinical research projects within a globally recognized CRO.
Key Responsibilities
Develop and validate bioanalytical methods in accordance with regulatory guidelines and laboratory standards.
Perform processing and analysis of biological samples for assigned clinical research projects.
Operate, calibrate, and troubleshoot LC-MS/MS systems and other analytical instruments used in bioanalytical testing.
Prepare draft method SOPs and ensure compliance with system-specific and method-specific SOPs, protocols, and study plans.
Ensure completion of required training on SOPs and documentation prior to initiating laboratory activities.
Maintain strict compliance with GLP requirements and 21 CFR Part 11 regulations related to electronic records and data integrity.
Verify instrument labeling, maintain accurate equipment logbooks, and ensure timely calibration of laboratory instruments.
Follow OECD GLP principles to maintain high standards of laboratory quality and regulatory compliance.
Core Competencies
Strong accountability and ownership of assigned laboratory activities.
Effective communication and documentation skills.
High work ethic and attention to detail in laboratory operations.
Good presentation and scientific reporting abilities.
Ability to work effectively within a collaborative and quality-focused organizational culture.
Educational Qualification
M.Pharm, B.Pharm, or M.Sc. in Pharmaceutical Sciences, Chemistry, Life Sciences, or a related discipline.
Preferred Skills
Hands-on experience with LC-MS/MS instrumentation and bioanalytical techniques.
Strong understanding of GLP guidelines, 21 CFR Part 11 compliance, and OECD GLP principles.
Experience in method development, validation, and sample analysis within a bioanalytical laboratory environment.
Ability to manage multiple research tasks and maintain detailed documentation.
How to Apply
Qualified candidates interested in advancing their careers in bioanalytical research and clinical development are encouraged to apply through the official Lambda Therapeutic Research careers portal or explore more pharmaceutical and clinical research job opportunities on ThePharmaDaily.com.
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