We are seeking a highly motivated and detail-oriented Analytical R&D; Qualified to support analytical development activities for CDMO projects. The candidate will be responsible for analytical method development, validation, stability studies, impurity profiling, and regulatory-compliant analytical documentation. The role requires solid expertise in chromatographic techniques and compliance with pharmaceutical quality standards

Key Responsibilities
Develop, optimize, and validate analytical methods using HPLC, UPLC, GC, and other analytical instruments.
Perform method validation, verification, and method transfer activities in accordance with ICH guidelines.
Conduct impurity profiling, forced degradation studies, and stability studies for APIs, intermediates, and drug substances.
Support Process R&D;, Manufacturing, Quality Assurance (QA), Quality Control (QC), and Regulatory Affairs teams.
Prepare, review, and maintain analytical protocols, reports, SOPs, specifications, and technical documentation.
Ensure compliance with cGMP, GLP, Data Integrity, and applicable regulatory requirements.

📌 Walk In Analytical Research Associate Senior Research Associate Hyderabad (India)
🏢 Aragen Life Sciences
📍 India