Experience

CV Sciences, Inc.

• United States
• Health, Wellness & Fitness
• 1 - 100 Employee

• QC Supervisor

  • May 2016 - Present

• Analytical Chemist

  • May 2016 - Present



Reckitt

• United Kingdom
• Manufacturing
• 700 & Above Employee

• R&D Assistant

  • Jun 2010 - Sep 2010

  1.Actively involved in monitoring and conducting stability studies of all healthcare, germ kill, personal care and surface care products to derive the shelf life. 2.As a part of Research and Development team, worked on analysis/testing of samples of new and existing product development. 3.Global update of new raw materials from different vendors used for different products. 4.Calibration and maintenance of all laboratory equipments. 5.Ensure strict adherence to GMP, GLP, COSHH assessment and health and safety standards. 6.Participated in internal auditing and checked for the compliance of quality. 7.Provide training to all fresher, based on previous experience at Reckitt Benckiser. Show less



Reckitt

• United Kingdom
• Manufacturing
• 700 & Above Employee

• Analytical Assistant in R &D (Nurofen Dept)

  • Oct 2009 - Apr 2010

  1.Active member of Method development and method validation team. 2.Stability testing of Nurofen products in accordance with ICH guidelines. 3.Use of Agilent and Waters HPLC system (Software: Empower), automated dissolution, disintegration, FTIR, pH meter and Water content by KF for analysis of various samples. 4.Interpreted data and reporting scientific results. 5.Plan and conduct experiments leading to the development and, or optimization of various analytical methods for active pharmaceutical ingredients, raw materials, intermediates, and finished products. 6.Author of method of analysis, validation protocol and report. 7.Preparation of Certificate of Analysis. 8.Extensive use of Documentum, TDS. 9.Member of HPLC maintenance team Show less



Bristol laboratories limited

• Luton, UK

• Quality Control Analyst

  • Sep 2008 - Sep 2009

  1.Undertake the routine testing of different finished products, intermediates and raw materials under GMP/GLP guidelines. 2.Physical and chemical Testing of Tablets and Capsules (Friability, Disintegration test, Dimensions & Hardness, Weighing, Loss on drying.) 3.Calibration of working standards. 4.Recording all documentation and review all associated analytical and laboratory data 5.Preparation and review of SOP’s, analytical methods and certificate of analysis. 6.Trained for OOS (Out of specification) investigation and preparing related documents. 7.Actively participated in internal and external audits. 8.Worked on Perkin elmer, shimadzu and kroma HPLC systems Show less