Research Associate - ADL

Role & responsibilities

• Routine Analysis: Plan and execute the analysis of formulation Development and Stability samples within predefined timelines.
• Instrument Upkeep: Ensure routine calibration and smooth operation of critical laboratory instruments (HPLC, Dissolution, UV-VIS, KF).
• Method Execution: Assist in developing stable analytical methods and completing their validation and subsequent transfer to plant QC labs.
• Documentation Compliance: Prepare, review, and finalize precise technical documents, including Specifications, STPs, and analytical reports.
• Timely Delivery: Review and submit accurate analytical reports promptly to minimize project lag times.
• Supervisory Oversight (For 4-5 Years Exp): Guide junior analysts, troubleshoot technical issues during analysis, and take responsibility for primary data review.
• Cross-Functional Coordination: Collaborate closely with Formulation R&D, Tech Transfer, and Quality Assurance teams to ensure seamless project progression.

Preferred candidate profile

• Equipment Operation & Calibration: Robust hands-on experience in operating and calibrating high-end instruments like HPLC, Dissolution Testers, UV-VIS Spectrophotometer, and Karl-Fischer (KF) titrators.
• Method Development & Validation: Strong foundational knowledge and practical execution of Analytical Method Development followed by Method Validation.
• Method Transfer: Experience in executing analytical method transfers to Receiving Laboratories (commercial manufacturing sites/QC).
• Compliance & Documentation: Thorough knowledge of Good Laboratory Practices (GLP), data integrity, and strict documentation management systems.
• Review & Reporting: Ability to prepare and review Specifications and Standard Testing Procedures (STP) in compliance with In-house and various Pharmacopoeias.