Job Opportunity: Research Associate / Senior Research Associate – Analytical Solutions (HPLC) at Aragen Life Sciences
Short Summary:
Aragen Life Sciences is seeking experienced analytical professionals for the role of Research Associate / Senior Research Associate at its Hyderabad facility. This is a full-time, lab-based position focusing on HPLC analysis, method development, and quality control. Interested candidates with 2–6 years of experience in the pharma/CRO industry are invited to attend our upcoming walk-in interview on April 5th, 2026.
About the Company
Aragen Life Sciences is a premier Contract Research, Development, and Manufacturing Organization (CRDMO) providing innovative solutions to the global pharmaceutical and biotech industries. We are committed to scientific excellence, regulatory compliance, and the highest standards of quality (GMP, ICH). Join our dynamic team as we continue to push the boundaries of drug discovery and development.
Role Overview
As an Analytical Research Associate, you will play a critical role in our Analytical Solutions department. You will be responsible for ensuring the quality and integrity of pharmaceutical products through precise testing, validation, and comprehensive reporting. This position requires a strong technical background in HPLC and a deep understanding of regulatory requirements in a fast-paced laboratory environment.
Key Responsibilities
1. Analytical & HPLC Operations:
- Perform routine and complex HPLC analyses, including Assay, Related Substances (RS), and Content testing.
- Conduct thorough analysis of raw materials, in-process samples, and finished pharmaceutical products.
- Execute dissolution testing for both stability and regular market release batches.
2. Method Development & Validation:
- Develop, refine, and validate analytical methods in accordance with global regulatory guidelines.
- Prepare detailed validation protocols, technical reports, and analytical summaries to support regulatory submissions.
3. Quality Control & Compliance:
- Perform routine QC analysis while strictly adhering to cGMP and GLP standards.
- Maintain accurate, real-time documentation for all laboratory activities.
- Investigate OOS (Out of Specification), OOT (Out of Trend), and deviations promptly, ensuring appropriate root cause analysis and corrective actions.
4. Instrumentation & Troubleshooting:
- Manage the calibration, qualification, and routine maintenance of analytical instruments.
- Proactively troubleshoot equipment issues to minimize downtime and ensure continuous laboratory operations.
Eligibility Criteria
- Educational Qualifications: M.Pharmacy or M.Sc. (Analytical Chemistry).
- Experience: 2–6 years of relevant experience in a Pharma or CRO setting.
- Core Skills: Proficiency in HPLC, analytical method development, regulatory compliance (ICH/GMP), technical documentation, and complex problem-solving in a laboratory setting.
Walk-In Interview Details
We are hosting a walk-in drive for all eligible candidates. Please bring your updated resume and relevant credentials.
- Date: 5th April 2026 (Sunday)
- Time: 10:00 AM – 1:00 PM
- Venue: Survey No. 125 & 126, IDA Mallapur, Hyderabad – 500076.
- Contact Information: For any queries or to submit your application in advance, please email your profile to [email protected].
Aragen Life Sciences is an equal opportunity employer. We value a diverse workforce and encourage all qualified individuals to apply.