Supply Chain Manager

• Mar 2020 - Present

SC Label Compliance Analyst

• May 2016 - Mar 2020

QC Lab Specialist

• Oct 2013 - Apr 2016

Assistant Scientist

• 2008 - 2013

•Experience with developing, validating, and implementing UPLC-PDA, UPLC-MS, methods for analysis of small molecules in accordance to ISO 17025 Guidelines and internal SOPs. •Proficient in Waters Alliance HPLC and Acquity UPLC instrument troubleshooting, maintenance and calibration verifications. •Reduced analysis costs and time by over 50% by developing, validating, and implementing an UPLC-PDA method for analysis of incoming ingredients for economic adulteration •Recommended and… Show more •Experience with developing, validating, and implementing UPLC-PDA, UPLC-MS, methods for analysis of small molecules in accordance to ISO 17025 Guidelines and internal SOPs. •Proficient in Waters Alliance HPLC and Acquity UPLC instrument troubleshooting, maintenance and calibration verifications. •Reduced analysis costs and time by over 50% by developing, validating, and implementing an UPLC-PDA method for analysis of incoming ingredients for economic adulteration •Recommended and implemented a new process for internal auditing which significantly improved the quality of findings, timeliness of reporting, and compliance to ISO 17025 •Achieved ISO 17025 accreditation for the laboratory for five years as quality systems coordinator which included the following responsibilities: •maintained all quality system documentation and correspondence to A2LA •performed all internal audits •implemented and maintained CAPA database •ensured compliance with the quality system •Decreased the down time on instruments by 20% by performing instrument calibration checks, preventive maintenance and troubleshooting activities on 12 HPLC systems and 2 UPLC systems •Supported the release process of ingredients by performing routine analysis utilizing HPLC, UPLC, refractometer, UV-Vis, and liquid/liquid extraction when necessary to maintain a 99% on-time completion rate Show less •Experience with developing, validating, and implementing UPLC-PDA, UPLC-MS, methods for analysis of small molecules in accordance to ISO 17025 Guidelines and internal SOPs. •Proficient in Waters Alliance HPLC and Acquity UPLC instrument troubleshooting, maintenance and calibration verifications. •Reduced analysis costs and time by over 50% by developing, validating, and implementing an UPLC-PDA method for analysis of incoming ingredients for economic adulteration •Recommended and… Show more •Experience with developing, validating, and implementing UPLC-PDA, UPLC-MS, methods for analysis of small molecules in accordance to ISO 17025 Guidelines and internal SOPs. •Proficient in Waters Alliance HPLC and Acquity UPLC instrument troubleshooting, maintenance and calibration verifications. •Reduced analysis costs and time by over 50% by developing, validating, and implementing an UPLC-PDA method for analysis of incoming ingredients for economic adulteration •Recommended and implemented a new process for internal auditing which significantly improved the quality of findings, timeliness of reporting, and compliance to ISO 17025 •Achieved ISO 17025 accreditation for the laboratory for five years as quality systems coordinator which included the following responsibilities: •maintained all quality system documentation and correspondence to A2LA •performed all internal audits •implemented and maintained CAPA database •ensured compliance with the quality system •Decreased the down time on instruments by 20% by performing instrument calibration checks, preventive maintenance and troubleshooting activities on 12 HPLC systems and 2 UPLC systems •Supported the release process of ingredients by performing routine analysis utilizing HPLC, UPLC, refractometer, UV-Vis, and liquid/liquid extraction when necessary to maintain a 99% on-time completion rate Show less

Sr. QC Associate

• 2007 - 2008

•Perform routine analysis of in-process, release, and stability samples in compliance with SOPs, STMs, and cGMP regulations utilizing HPLC and SDS-PAGE methodologies •Integral member of QC team whose responsibilities included: testing of new analytical procedures for clarity and ease of use, revising documentation to ensure accurate data reporting, facilitate method transfer from R&D to QC, and act as liaison between R&D and QA •Perform routine analysis of in-process, release, and stability samples in compliance with SOPs, STMs, and cGMP regulations utilizing HPLC and SDS-PAGE methodologies •Integral member of QC team whose responsibilities included: testing of new analytical procedures for clarity and ease of use, revising documentation to ensure accurate data reporting, facilitate method transfer from R&D to QC, and act as liaison between R&D and QA

Analytical Chemist

• 1998 - 2006

•Developed, implemented, and maintained sample submission procedures and data reporting in accordance with ISO 17025 guidelines which significantly improved communication and traceability of work •Utilized organizational skills to coordinate and manage sample preparation, instrumental analysis, and data review for three senior level chemists which enabled faster turn around times for results •Determined and met internal customers’ analytical needs for over 20 projects by performing… Show more •Developed, implemented, and maintained sample submission procedures and data reporting in accordance with ISO 17025 guidelines which significantly improved communication and traceability of work •Utilized organizational skills to coordinate and manage sample preparation, instrumental analysis, and data review for three senior level chemists which enabled faster turn around times for results •Determined and met internal customers’ analytical needs for over 20 projects by performing routine and non-routine analysis of prototypes that incorporated new technologies •Supervised and evaluated the work of up to four laboratory technicians to support a product aging study and routine analyses Show less •Developed, implemented, and maintained sample submission procedures and data reporting in accordance with ISO 17025 guidelines which significantly improved communication and traceability of work •Utilized organizational skills to coordinate and manage sample preparation, instrumental analysis, and data review for three senior level chemists which enabled faster turn around times for results •Determined and met internal customers’ analytical needs for over 20 projects by performing… Show more •Developed, implemented, and maintained sample submission procedures and data reporting in accordance with ISO 17025 guidelines which significantly improved communication and traceability of work •Utilized organizational skills to coordinate and manage sample preparation, instrumental analysis, and data review for three senior level chemists which enabled faster turn around times for results •Determined and met internal customers’ analytical needs for over 20 projects by performing routine and non-routine analysis of prototypes that incorporated new technologies •Supervised and evaluated the work of up to four laboratory technicians to support a product aging study and routine analyses Show less