| Resume alert | Resumes 41 - 50 of 103 |
Sales Supply Chain
Overland Park, KS, 66221
... Spearheaded full regulatory recovery in 14 months resulting in zero FDA observations and achieved full product recertification within three months. Optimized asset base to align to new product portfolio to drive target profitability, resulting in ... - 2018 Apr 03
... Spearheaded full regulatory recovery in 14 months resulting in zero FDA observations and achieved full product recertification within three months. Optimized asset base to align to new product portfolio to drive target profitability, resulting in ... - 2018 Apr 03
Manager Customer Service
Kansas City, KS
... Maintained all paperwork associated from the collection of specimens, including shipping those samples according to SOP’s provided by the FDA Education B.S. – Bachelors of Science University of Missouri Kansas City A.S – Associates of Science Penn ... - 2018 Mar 30
... Maintained all paperwork associated from the collection of specimens, including shipping those samples according to SOP’s provided by the FDA Education B.S. – Bachelors of Science University of Missouri Kansas City A.S – Associates of Science Penn ... - 2018 Mar 30
Product Development Engineer
Kansas City, MO
... Provide audit and regulatory support for FDA, CSA, U/L, Intertek & TUV (Notified Bodies). STRYKER INSTRUMENTS, MI (continued) staff Compliance Engineer Key Achievements: EU environmental programs REACH, RoHS, WEEE and Prop 65 for hazardous chemical ... - 2017 Apr 27
... Provide audit and regulatory support for FDA, CSA, U/L, Intertek & TUV (Notified Bodies). STRYKER INSTRUMENTS, MI (continued) staff Compliance Engineer Key Achievements: EU environmental programs REACH, RoHS, WEEE and Prop 65 for hazardous chemical ... - 2017 Apr 27
Manager Data Entry
Blue Springs, MO
... I have received numerous FDA MedWatch citations for participation and diligence toward reporting adverse events. Medication Therapy Management certification. I have been published once by name and about 200 times anonymously in the medical ... - 2017 Mar 16
... I have received numerous FDA MedWatch citations for participation and diligence toward reporting adverse events. Medication Therapy Management certification. I have been published once by name and about 200 times anonymously in the medical ... - 2017 Mar 16
Engineer Microsoft Office
Overland Park, KS
... and Investigator/Staff Training Plans Created reports of adverse events in compliance with IRB stipulations and in accordance with FDA regulations and ICH guidelines Designed Informed Consent Form, Patient Questionnaire, and Subject Monitoring Logs ... - 2017 Jan 23
... and Investigator/Staff Training Plans Created reports of adverse events in compliance with IRB stipulations and in accordance with FDA regulations and ICH guidelines Designed Informed Consent Form, Patient Questionnaire, and Subject Monitoring Logs ... - 2017 Jan 23
Engineer Manufacturing
Kansas City, KS
... Developing and writing documentation as SOP’s, work instructions, personal training complied with ISO and FDA regulation to maintain a consistent and repeatable molding manufacturing process. Procurement, capital justification, reviews and approves ... - 2017 Jan 13
... Developing and writing documentation as SOP’s, work instructions, personal training complied with ISO and FDA regulation to maintain a consistent and repeatable molding manufacturing process. Procurement, capital justification, reviews and approves ... - 2017 Jan 13
SAP implementations, Inventory, Manufacturing and Warehouse experience
Kansas City, MO
... Wrote and updated SOP’s and was liaison person for FDA inspections. Team Member/Processor/Technician: Worked in all areas of the pharmaceutical manufacturing process to include: handling, weighing, granulating, compression and coating tablets. ... - 2016 Nov 30
... Wrote and updated SOP’s and was liaison person for FDA inspections. Team Member/Processor/Technician: Worked in all areas of the pharmaceutical manufacturing process to include: handling, weighing, granulating, compression and coating tablets. ... - 2016 Nov 30
Management Real Estate
Shawnee, KS, 66218
... FDA facility advisor responsible for all compliance procedure reports and audits. Contact for compliance with GMP and CFR21. Designed and installed compressed air and vacuum systems. Traveled to other units outside of Kansas City and designed / ... - 2016 Nov 30
... FDA facility advisor responsible for all compliance procedure reports and audits. Contact for compliance with GMP and CFR21. Designed and installed compressed air and vacuum systems. Traveled to other units outside of Kansas City and designed / ... - 2016 Nov 30
Manager Project
Peculiar, MO, 64078
... Key Achievements: Ensured facility maintained certifications with GMPs, BRC, AIB, ISO, HACCP, and FDA. Handled all facility scheduling including overtime, sick days, vacation, and more. Additional Experience Warehouse Supervisor, American ... - 2016 Aug 20
... Key Achievements: Ensured facility maintained certifications with GMPs, BRC, AIB, ISO, HACCP, and FDA. Handled all facility scheduling including overtime, sick days, vacation, and more. Additional Experience Warehouse Supervisor, American ... - 2016 Aug 20
VP/Director of Operations
Overland Park, KS
... Director of Manufacturing and Operations (2011 – 2015) Responsible for P&L, manufacturing operations, facilities management of a 120 person, $120M ISO 9001:2008/14001:2004/OHSAS 18001:2007/ ITAR/FDA compliant high mix/low volume factory. Achieved ... - 2016 Jul 12
... Director of Manufacturing and Operations (2011 – 2015) Responsible for P&L, manufacturing operations, facilities management of a 120 person, $120M ISO 9001:2008/14001:2004/OHSAS 18001:2007/ ITAR/FDA compliant high mix/low volume factory. Achieved ... - 2016 Jul 12