Dear Sir, We are hiring Analysts for our IVRT/IVPT team. Please go through below JD, and share your profiles on harisha.p@invitron.co.in or contact us on 9000251866,if JD suits you. Experience Required: 2 to 6 years (pharmaceutical / CRO industry) Location: Plot No.126,ALEAP Industrial Estate, Pragathinagar, Hyderabad - 90. Department: Analytical Research Key Responsibilities Design, plan, and execute in-vitro permeation testing (IVPT) and in-vitro release testing (IVRT) studies for topical, transdermal, and semi-solid dosage forms in line with regulatory guidance (FDA, EMA). Develop, validate, and implement bioanalytical methods for IVPT/IVRT studies using LC-MS/MS (Sciex systems preferred). Perform method transfers, optimization, and troubleshooting on LC-MS/MS, UPLC and HPLC platforms. Conduct sample preparation, extraction, and quantification for study samples. Ensure GLP compliance and maintain data integrity, documentation, and audit readiness throughout study execution. Prepare and review study protocols, analytical method validation reports, and study reports as per regulatory expectations. Qualifications Masters in Pharmaceutical Sciences, Analytical Chemistry, or related discipline. Strong experience in IVPT and IVRT studies for topical/transdermal formulations. Hands-on expertise in LC-MS/MS (Sciex, Agilent and shimadzu) operation, calibration, troubleshooting, and method development/validation. Knowledge of FDA, EMA, and OECD regulatory guidelines relevant to IVPT/IVRT and bioanalytical method validation. Experience in handling study samples Key Skills Expertise in bioanalytical method development using LC-MS/MS. Strong knowledge of skin permeation, release kinetics, and topical drug delivery. Detail-oriented with strong documentation and regulatory compliance mindset. Good communication and cross-functional collaboration skills. Regards Team HR.