Job Description
· Perform method development, method validation, method transfer, and routine analytical activities for OSD formulations.· Conduct analysis using HPLC, GC, UV-Visible Spectrophotometer, Dissolution Apparatus, FTIR, and other analytical instruments.· Prepare analytical protocols, reports, specifications, SOPs, STPs, and related documentation.· Execute stability sample analysis and support product development activities.· Ensure compliance with cGMP, GLP, Data Integrity, and regulatory requirements.· Maintain laboratory records, logbooks, and instrument calibration/qualification documentation.· Investigate OOS, OOT, and laboratory deviations as per approved procedures.· Coordinate with Formulation Development, QA, QC,



and Regulatory Affairs teams for project execution.· Participate in audits and regulatory inspections as required.Required Skills:· Hands-on experience with HPLC and dissolution testing.· Knowledge of analytical method validation and stability studies.· Understanding of ICH guidelines, cGMP, and GLP requirements.· Valuable documentation and report-writing skills.· Proficiency in MS Office applications.Preferred Candidate Profile:· Experience in OSD pharmaceutical formulation analysis.· Good analytical and problem-solving skills.· Ability to work independently and within cross-functional teams.

📌 Research Associate (Ahmedabad)
🏢 Corona Remedies
📍 Ahmedabad