Research Associate – Bioanalytical Operations
Lambda Therapeutic Research Ltd. | Ahmedabad, India
Experience Required: 2-3 years
Salary (CTC): INR 3,00,000 – 5,00,000 per annum
Job ID: 1363
Posted On: 15 November 2025
Location: Ahmedabad, Gujarat
About the Company
Lambda Therapeutic Research Ltd. is a global, full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operational footprints across Mehsana (India), Las Vegas (USA), Pittsburgh (USA), Toronto (Canada), Warsaw (Poland), and London (UK), Lambda delivers comprehensive clinical research solutions to innovator, biotech, and generic pharmaceutical companies worldwide.
The organization is known for its scientific expertise, advanced bioanalytical capabilities, and strong compliance culture aligned with international regulatory standards.
Role Overview
Lambda is hiring a Research Associate – Bioanalytical Operations to support method development, sample analysis, and instrument operations within the bioanalytical division. This role is suitable for freshers who want to build a strong technical foundation in bioanalysis, LC-MS/MS operations, and regulated laboratory environments.
Key Responsibilities
Bioanalytical Method Development & Validation
Assist in developing, optimizing, and validating bioanalytical methods as per project requirements.
Support method execution according to study plans, protocols, and SOPs.
Sample Processing & Analysis
Process and analyze biological samples for assigned studies.
Maintain accuracy, compliance, and timely reporting of analytical results.
Instrument Handling & Calibration
Operate and handle LC-MS/MS and other analytical instruments.
Support calibration, troubleshooting, and routine instrument functionality checks.
Documentation & SOP Compliance
Prepare draft SOPs, method documents, and ensure adherence to system/method-specific SOPs.
Complete mandatory SOP training before initiating any activity.
Maintain logbooks, equipment labels, and calibration records in compliance with GLP expectations.
Quality & Regulatory Compliance
Ensure implementation of GLP, OECD principles, and 21 CFR Part 11 requirements.
Support internal audits by maintaining accurate documentation and instrument records.
Qualifications
M.Pharm / M.Sc. / B.Pharm
Strong interest in bioanalytical research, LC-MS/MS operations, and regulated lab environments.
2-3 years experience with academic or project exposure in analytical techniques will be preferred.
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | Tarasadi | Vadodara | Vapi |Maharashtra :
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Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
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Carlow |Republic of Ireland :
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Donegal |Meath :
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Netherlands |Remote Australia :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Sheffield |Oxfordshire :
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Australia | North York | Mississauga | Richmond Hill | Uxbridge | Renfrew |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
Zaventem |South America :
Peru | Argentina |Brazil :
Sao paulo | Brazil |Attica :
Athens | Koropi |Greece :
Greece |North Island :
Auckland |New Zealand :
New Zealand |Austria :
Austria |Vienna :
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Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
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