Lambda Therapeutic Research Ltd. has announced a recruitment opportunity for a Research Associate in its Bioanalytical Operations department in Ahmedabad, Gujarat. The vacancy is suitable for candidates with a background in Pharmacy or Science and relevant experience in bioanalytical research.
The role involves bioanalytical method development and validation, sample analysis, operation and troubleshooting of LC-MS/MS and other analytical instruments, preparation of SOPs, and compliance with GLP and 21 CFR Part 11 requirements.
According to the recruitment details, candidates with 2 to 3 years of experience and qualifications such as M.Pharm, B.Pharm, or M.Sc. can apply. The advertised CTC range for this position is ₹3.5 lakh to ₹5.5 lakh per year.
Lambda Therapeutic Research Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Lambda Therapeutic Research Ltd. |
| Job Title on Listing | Research Scientist |
| Designation in Job Details | Research Associate |
| Department | Bioanalytical Operations |
| Job Location | Ahmedabad, Gujarat |
| Req ID | 1562 |
| Experience | 2–3 Years |
| Qualification | M.Pharm / B.Pharm / M.Sc. |
| CTC Range | ₹3,50,000 – ₹5,50,000 per year |
| Date of Listing | September 19, 2026 |
| Industry | Clinical Research / Bioanalytical Research |
About Lambda Therapeutic Research
Lambda Therapeutic Research is a global Contract Research Organization (CRO) headquartered in Ahmedabad, India. The organization provides clinical research services to innovator, biotechnology, and generic pharmaceutical companies.
According to the company information provided in the vacancy, Lambda Therapeutic Research has facilities and operations in locations including India, the United States, Canada, Poland, and the United Kingdom, supporting its global clinical research operations.
Job Description – Research Associate
The Research Associate will work within the Bioanalytical Operations team and contribute to laboratory activities related to bioanalytical method development, validation, sample processing, analytical testing, instrument operation, and regulatory-quality compliance.
The role requires practical knowledge of analytical laboratory instruments and the ability to perform assigned project activities according to applicable protocols, plans, SOPs, and quality requirements.
Key Responsibilities
The major responsibilities associated with this position include:
- Develop and validate bioanalytical methods according to project requirements.
- Process and analyze samples assigned to individual projects.
- Operate LC-MS/MS instruments and other analytical laboratory equipment.
- Perform instrument calibration and support troubleshooting activities when required.
- Prepare draft analytical methods and relevant SOP documentation.
- Follow system-specific and method-specific SOPs during laboratory activities.
- Perform work according to applicable plans and study protocols.
- Complete required training on SOPs and controlled documents before starting relevant activities.
- Support implementation of Good Laboratory Practice (GLP) requirements.
- Follow 21 CFR Part 11 requirements applicable to computerized systems and laboratory activities.
- Check instrument labels and ensure equipment identification is properly maintained.
- Review equipment and instrument logbooks for completeness.
- Monitor calibration due dates and ensure instruments are calibrated within the required timeframe.
- Perform laboratory activities in accordance with OECD GLP principles.
- Maintain appropriate documentation and records related to assigned laboratory work.
Bioanalytical Operations Responsibilities
The position is primarily associated with bioanalytical laboratory activities. Candidates should be comfortable working with analytical instruments, sample analysis, method development, validation, documentation, and laboratory quality systems.
Hands-on exposure to LC-MS/MS is particularly relevant because the job description specifically includes instrument operation, calibration, and troubleshooting.
Educational Qualification
Candidates should possess any of the following qualifications:
- M.Pharm
- B.Pharm
- M.Sc.
The vacancy does not specify a particular M.Sc. specialization in the provided information.
Experience Requirements
The required experience is 2 to 3 years.
Candidates with relevant experience in bioanalytical laboratory operations, analytical testing, method development, method validation, and analytical instrumentation may find the responsibilities aligned with their professional background.
Required Skills
The role requires skills and knowledge related to:
- Bioanalytical method development
- Bioanalytical method validation
- Sample processing and analysis
- LC-MS/MS operation
- Analytical instrument troubleshooting
- Instrument calibration
- SOP preparation and compliance
- Laboratory documentation
- GLP practices
- OECD GLP principles
- 21 CFR Part 11 compliance
- Equipment and instrument logbook management
- Protocol and study-plan compliance
- Laboratory quality systems
GLP and Regulatory Compliance
Quality and regulatory compliance are important components of this position. The Research Associate is expected to work according to applicable GLP and OECD GLP principles and support compliance with 21 CFR Part 11.
The responsibilities include checking instrument labels, maintaining complete equipment and instrument logbooks, and ensuring calibration activities are completed before their due dates.
Job Location
The position is based in:
Ahmedabad, Gujarat, India
The vacancy does not specify a remote or hybrid work arrangement, so candidates should refer to the employer’s official recruitment communication for the applicable work setup.
Salary / CTC
The advertised CTC range for this position is:
₹3,50,000 to ₹5,50,000 per year
The actual compensation offered to an individual candidate may depend on the company’s recruitment terms and the candidate’s qualifications and experience.
Selection Process
The supplied vacancy information does not provide details of the selection process.
Candidates should therefore refer to the company’s recruitment communication for information regarding interviews, assessments, technical discussions, or other selection stages, if applicable.
How to Apply
Interested candidates should apply through the official Lambda Therapeutic Research careers portal and search for the relevant Research Scientist / Research Associate vacancy using Req ID 1562.
The supplied vacancy page identifies the position as Research Scientist, while the job details list the designation as Research Associate. Candidates should verify the exact designation shown on the application page before submitting their application.
Important Details Before Applying
- Company: Lambda Therapeutic Research Ltd.
- Req ID: 1562
- Job Title: Research Scientist
- Designation: Research Associate
- Department: Bioanalytical Operations
- Location: Ahmedabad, Gujarat
- Experience: 2–3 years
- Qualification: M.Pharm / B.Pharm / M.Sc.
- CTC: ₹3.5–₹5.5 LPA
- Key Instrument: LC-MS/MS
- Date Listed: September 19, 2026
- Important Compliance Areas: GLP, OECD GLP and 21 CFR Part 11
Frequently Asked Questions
1. What position is available at Lambda Therapeutic Research?
The recruitment listing is titled Research Scientist, while the job details identify the designation as Research Associate.
2. Where is this job located?
The position is based in Ahmedabad, Gujarat, India.
3. Which department is hiring?
The vacancy is within the Bioanalytical Operations department.
4. What qualifications are required?
Candidates with M.Pharm, B.Pharm, or M.Sc. qualifications can apply according to the provided vacancy details.
5. How much experience is required?
The position requires 2 to 3 years of experience.
6. What is the salary offered?
The advertised CTC range is ₹3,50,000 to ₹5,50,000 per year.
7. Is LC-MS/MS experience relevant to this position?
Yes. The job responsibilities specifically include operating, calibrating, and troubleshooting LC-MS/MS instruments and other analytical instruments.
8. What are the major responsibilities of the Research Associate?
The role includes bioanalytical method development and validation, sample analysis, analytical instrument operation, SOP preparation, documentation, calibration monitoring, and compliance with GLP and 21 CFR Part 11 requirements.
9. Does the role involve GLP compliance?
Yes. The job description specifically requires implementation of GLP and OECD GLP principles.
10. What is the recruitment reference number?
The requisition ID for this vacancy is 1562.
Important Note
Recruitment information can be changed or updated by the employer. Candidates should verify the latest job title, designation, eligibility criteria, CTC, application status, and recruitment requirements on the official Lambda Therapeutic Research careers portal before applying.