Cadila Pharmaceuticals Hiring Research Associate – Pre-Clinical
- Exciting Opportunity in Pre-Clinical Research at Cadila Pharmaceuticals Ltd.
- About Cadila Pharmaceuticals
- Research Associate – Pre-Clinical Department
- Key Responsibilities
- Qualifications & Experience
- Required Educational Background
- Experience
- Skills and Competencies
- Location and Facility
- Why Cadila Pharmaceuticals?
- How to Apply
- Summary Table
M.Pharm/MSc Pre-Clinical Research Jobs | 3+ Years Experience at Cadila Pharma, Ahmedabad
Apply now for Pre-Clinical Research Associate jobs at Cadila Pharmaceuticals Ltd., Dholka – Ahmedabad. Openings for M.Pharm/MSc with 3+ years experience.
Exciting Opportunity in Pre-Clinical Research at Cadila Pharmaceuticals Ltd.
Cadila Pharmaceuticals Ltd., one of India’s largest privately held pharma companies, is actively hiring experienced professionals in its Pre-Clinical Research division (CRO – Pre-Clinical) for the Research Associate role at Dholka, Ahmedabad. This is an excellent opportunity for life science postgraduates with strong pre-clinical and toxicology backgrounds.
About Cadila Pharmaceuticals
With over six decades of innovation, Cadila Pharmaceuticals is a global pioneer in life sciences and drug discovery. It is committed to delivering affordable healthcare solutions across 100+ countries and complies with international regulatory standards like USFDA, MHRA, and WHO-GMP.
Research Associate – Pre-Clinical Department
Key Responsibilities
- Act as Study Director for GLP toxicology studies in certified facilities
- Conduct, schedule, and report toxicological and pharmacological evaluations for various drug formulations
- Ensure GLP compliance, regulatory documentation, and SOP adherence
- Collaborate with cross-functional teams for regulatory audits and facility inspections
- Maintain study documentation as per OECD and GLP guidelines
Qualifications & Experience
Required Educational Background
- Master’s in Pharmacy (M.Pharm)
- Master’s in Science (MSc – preferably Life Sciences or Pharmacology)
Experience
- Minimum 3 years of hands-on experience in a GLP-compliant pre-clinical/toxicology research setup
Skills and Competencies
- Strong understanding of pre-clinical toxicology protocols
- Good command over SOP writing and documentation
- Experience with regulatory study design and reporting
- Strong organizational and leadership capabilities
Location and Facility
- Job Location: Dholka, Ahmedabad (R&D Facility)
- Facility Type: CRO – Pre-Clinical
- Work Mode: Full-time
Why Cadila Pharmaceuticals?
- Work in globally accredited GLP research facilities
- Join a research-driven environment with growth opportunities
- Be part of innovative drug discovery projects impacting global health
How to Apply
Send your CV to disha.bhalani@cadilapharma.com with subject line: Application – Pre-Clinical Research Associate
Summary Table
| Company Name | Cadila Pharmaceuticals Ltd. |
|---|---|
| Current Vacancies | Research Associate – Pre-Clinical |
| Required Education | M.Pharm, MSc |
| Experience Required | Minimum 3 Years |
| Location | Dholka, Ahmedabad |
To apply for this job email your details to disha.bhalani@cadilapharma.com
