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RESEARCH ASSOCIATE
Corona Remedies · Ahmedabad, India
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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. · Good 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.