Material testing & Qualification. Extractables and Leachables in Medical devices EP, USP Pharmacopeia compliance testing on disposable, packaging, and container closure materials and container systems. Identify existing alternative methods and technologies for improving existing or new products/processes.Method development and Validation.

1. Responsible for pharma packaging analysis based on USP 661.1 and 661.2(Plastic Materials of Construction)2. To process the regular analysis for the determination of RoHS(PBBs, PBDEs) as per IEC 62321:2015, RoHS Heavy metals as per IEC 62321:2013, Phthalates as per EN 14372 and CPSC, PAH as per AfPS GS 2014 in Material Samples.3. To conduct the qualitative and quantitative analysis for REACH-191 and Overall and Specific migration of FCM as per EU,IS,GB,US FDA and BfR.4. Preparation of Standard operating procedures for the validated analytical methods in the relevant field.5. Responsible for food contact Material testing section Test Execution.6. Responsible for Food contact material testing as per IS 9845,IS9833,LFGBSEC30& 31, EU 10/2011, 21 CFR 177.1520,1630,2600,176.170,2010 etc...7. Responsible for handling, operations, Maintenance, Troubleshooting of HS-GC-FID/ECD /MS and GC-MS/MS, ICP-OES.8. Responsible for handling and operations of GC-MS-HS for Food-Material-HPC(Homecare-Personalcare-Cosmetics )parameters for various Residual solvents as Per USP-467, EN 13628-2:2004, Inhouse methods .9. Food contact materials as per EU, IS,GB,USFDA and BfR regulations.10. RoHS testing as per EC 65/2011.11. REACH-191 testing as per EC 1907/2006.

1. Maintaining Certified reference materials, chemicals required.2. Ensuring the purity & validity of standard solutions and CRMS3. Preparation of stock and working standard solutions. 4. Ensuring traceability of all reference materials & calibration of equipments.

Project work on estimation of doxofylline 400mg tablets by HPLC(Assay,RS by HPLC and Dissolution Studies)