Research associate for Bioanalytical

Company Description Lambda Therapeutic Research is a leading full-service global Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with additional facilities in India, the USA, Canada, the UK, Spain, and Poland. The organization provides end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies, covering early to late phase trials and specialized services. With a team of over 1,200 professionals, Lambda uses advanced technology and innovative approaches to deliver high-quality clinical trial solutions. The company has received multiple industry recognitions, including awards for regulatory excellence, workplace quality, and partnership in generics and biosimilars. Its service portfolio includes Phase I studies, BA/BE, bioanalytical services, data management, medical imaging, pharmacovigilance, biosimilars development, medical and scientific writing, and clinical lab services.
Role Description This is a full-time, on-site role for a Research Associate – Bioanalytical based in Ahmedabad. The role involves performing bioanalytical testing and sample analysis for clinical and preclinical studies using validated analytical methods and instruments (such as LC-MS/MS and HPLC). Responsibilities include preparing biological samples, executing assays, maintaining detailed laboratory records, and ensuring adherence to SOPs, GLP, and regulatory guidelines. The Research Associate will assist in method development and validation, support troubleshooting of analytical issues, and collaborate with cross-functional study teams to meet project timelines. The role also includes routine calibration and maintenance of laboratory equipment, participation in audits and inspections, and contributing to continuous improvement of bioanalytical workflows.
Qualifications
Candidates should possess strong bioanalytical and laboratory skills, including sample preparation, chromatography techniques, and quantitative analysis of drugs and metabolites.
Candidates should possess skills in method development and validation, assay optimization, and troubleshooting analytical procedures.
Candidates should possess knowledge of regulatory and quality standards such as GLP, GCP, FDA, EMA, and OECD guidelines, along with thorough understanding of SOPs and documentation practices.
Candidates should possess skills in data handling and interpretation, including use of analytical software, basic statistics, and preparation of technical reports and documentation.
Candidates should possess strong attention to detail, organizational skills, and the ability to work collaboratively in a fast-paced, project-driven environment.
Relevant educational background such as a bachelor’s or master’s degree in Pharmacy, Biotechnology, Biochemistry, Chemistry, or a related life science field is preferred.
Prior experience in a bioanalytical laboratory or CRO setting, especially in BA/BE or clinical bioanalysis, will be an advantage.
Good written and verbal communication skills and readiness to work in shifts as per project requirements are

Work arrangement
No