Lambda Therapeutic Research Ltd., a global full-service Clinical Research Organization, has announced a hiring opportunity for the position of Research Executive in Ahmedabad. This role is suitable for candidates experienced in method validation report writing, especially for PK, PD, immunogenicity assays, small molecules, biologics, and biosimilars.
The selected candidate will work as an MV report writer, preparing method validation reports as per GLP and non-GLP regulatory guidelines. For life science professionals looking to build a career in clinical research documentation, bioanalytical reporting, and regulatory-compliant scientific writing, this is a strong opportunity.
Job Overview
| Details | Information |
|---|---|
| Company | Lambda Therapeutic Research Ltd. |
| Role | Research Executive |
| Req ID | 1584 |
| Location | Ahmedabad, India |
| Job Type | Full-time |
| Experience | 2+ years |
| Qualification | MSc in Biotechnology, Biochemistry, or Life Science |
| Salary | ₹4,00,000 – ₹8,00,000 per year |
| Posted Date | July 26, 2026 |
| Last Date | Not specified |
Responsibilities
As a Research Executive at Lambda Therapeutic Research, the candidate will be responsible for:
- Preparing method validation reports for PK, PD, and immunogenicity assays.
- Writing MV reports for small molecules, biologics, and biosimilars as per GLP and non-GLP regulatory guidelines.
- Coordinating with the operations team to collect and compile relevant method validation data.
- Working with Quality Control and Quality Assurance teams for QC and QA review of MV reports.
- Resolving QC and QA queries related to method validation report preparation.
- Ensuring proper formatting, review readiness, and finalization of MV reports.
- Maintaining tracking records for method validation report timelines.
- Preparing, updating, and maintaining SOPs related to MV report writing.
Qualifications: Who Can Apply?
Candidates can apply if they have:
- MSc in Biotechnology
- MSc in Biochemistry
- MSc in Life Science
The job description clearly asks for candidates with 2 or more years of MV report writing experience in small molecules, biologics, or biosimilars as per regulatory guidelines.
Skills Required
Technical Skills
- Method validation report writing
- PK/PD assay documentation
- Immunogenicity assay reporting
- GLP and non-GLP guideline understanding
- SOP preparation and maintenance
- Scientific report formatting
Domain Skills
- Clinical research documentation
- Bioanalytical method validation
- Small molecule studies
- Biologics and biosimilar studies
- QC and QA review coordination
- Regulatory-compliant documentation
Soft Skills
- Attention to detail
- Timeline management
- Cross-functional coordination
- Query resolution
- Documentation accuracy
- Communication skills
Salary
The company has mentioned a CTC range of:
₹4,00,000 – ₹8,00,000 per year
Salary may vary depending on experience, report writing expertise, and relevant exposure to GLP/non-GLP method validation documentation.
Benefits
Benefits were not clearly specified in the job description.