Testing of Restricted Substances in Fabric,Leather,Plasticisers and other products by using different Instruments like GCMS,LCMS,FTIR,UV-vis and other wet processes.

. Quantitative determination of 26 different banned Aromatic Amines derived from AZO dyes in Leather, Paint, Print and different textile materials using GC-MS and HPLC-DAD. Sample breakdown for AZO, Applicable part and material, Compositing testing, Test methods (EN 14362-1&3). Wet process for testing of AZO dyes in textile materials, quality parameters, analysis and result calculation.

. Quantitative determination of banned Phthalates and their derivatives used in plasticizers, leather and printing materials by using GC-MS and LC-MS. Sample breakdown for Phthalate, Compositing testing, Applicable part and material, Test methods (CPSC, EN, ISO 14389:2014). Wet process for testing of Phthalates, quality parameters, analysis and result calculation.

. Quantitative determination of banned Chlorinated Phenols (MoCP, DiCP, TriCP, TeCP, PCP) in leather products and textile materials by using GC-MS. Sample breakdown for CP, Test methods DIN EN ISO 17070:2015-05, EN ISO 17070:2015 (E). Wet process for testing of Chlorinated Phenols in leather and textile materials, quality parameters, analysis and result and calculation.

. Quantitative determination of Formaldehyde used in leather products by using HPLC-DAD, Test method ISO 17226-1 2008(E), Wet process for testing of Formaldehyde, quality parameters, analysis and result calculation.

. Worked on a case study \"Possibilities of Hexavalent Chromium (Cr-VI) generation in Chrome Tanning Process, situations at which Cr-III converted into Cr-VI, Possible preventive and corrective measures\".

. Pre-Trearment of Fabric
. Dying of Fabric
. Finishing of Fabric

. Sampling and testing of raw materials, intermediates and finished products using current pharmacopeias, any associated ‘wet’ chemistry and instrumental technique (HPLC, IR, UV), as appropriate.
. Preparing Quality reports, including analytical reports (for raw materials and finished products),Certificates of Analysis (CoA) (for finished products) and stability reports.
. Creating and executing method development and method validation test protocols for finished products and generating the appropriate analytical methods.
. Stability testing of products for new formulations and ongoing stability trials, using physical (pH,viscosity) and instrumental (HPLC, UV) techniques, as appropriate
. Writing analytical specifications using current pharmacopoeias and reviewing existing analytical specification.
. Writing/reviewing Standard Operating Procedures (SOPs).
. Calibrating analytical equipment, as and when required.
. Supporting all QC activities.
. Observing and complying with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP).
. Observing and complying with company Health and Safety Policies.
. Observing and complying with company Standard Operating Procedures (SOPs).