| Resume alert | Resumes 81 - 90 of 305 |
Manager Quality
Emmaus, PA
... Experience: QuVa Pharma – Bloomsbury, NJ October 2018 – February 2019 Manager, Quality Systems - Laboratory Responsible for ensuring that all laboratory investigations are conducted in compliance with internal procedures and FDA regulations. ... - 2019 Mar 05
... Experience: QuVa Pharma – Bloomsbury, NJ October 2018 – February 2019 Manager, Quality Systems - Laboratory Responsible for ensuring that all laboratory investigations are conducted in compliance with internal procedures and FDA regulations. ... - 2019 Mar 05
Project Manager
Allentown, PA
... Developed and implemented internal Protocol Operational Review process of clinical draft protocols prior to IRB/FDA submissions for Japanese headquartered pharmaceutical company in order to increase clinical trial protocol validity and acceptance ... - 2019 Feb 13
... Developed and implemented internal Protocol Operational Review process of clinical draft protocols prior to IRB/FDA submissions for Japanese headquartered pharmaceutical company in order to increase clinical trial protocol validity and acceptance ... - 2019 Feb 13
Mechanical Design
Pottstown, PA
... Terumo Medical Corporation - Elkton MD, New Product Development Design & Technology Co-Op March - September 2016 • Conduct Design of Experiments and other related processes for the improvement of and FDA compliance of catheter manufacturing while ... - 2019 Feb 08
... Terumo Medical Corporation - Elkton MD, New Product Development Design & Technology Co-Op March - September 2016 • Conduct Design of Experiments and other related processes for the improvement of and FDA compliance of catheter manufacturing while ... - 2019 Feb 08
Product Manager / Technical Writer
Gilbertsville, PA
... for protocols, reports, SOPs, MBRs, change control, product /process verification/validation protocols (IQ, OQ, PQ), and training materials to support production, QA, FDA 21 CFR Parts 210/211 and compliance requirements for new product launches. ... - 2018 Dec 11
... for protocols, reports, SOPs, MBRs, change control, product /process verification/validation protocols (IQ, OQ, PQ), and training materials to support production, QA, FDA 21 CFR Parts 210/211 and compliance requirements for new product launches. ... - 2018 Dec 11
Research Scientist, Medical writer/editor
Colmar, PA
... to submission process Strong working knowledge of clinical trials stages and drug development process, ICH guidelines, GCP, GLP, GMP principles, site monitoring, and audit process, medical and regulatory affairs such as IRB and FDA Education Ph.D. ... - 2018 Nov 29
... to submission process Strong working knowledge of clinical trials stages and drug development process, ICH guidelines, GCP, GLP, GMP principles, site monitoring, and audit process, medical and regulatory affairs such as IRB and FDA Education Ph.D. ... - 2018 Nov 29
Data Management
TATAMY Borough, PA, 18045
... -Applied Good Manufacturing Principles to be FDA complaint. -Resolve escalated issues as per Service Level Agreements. -Managed DNS, NFS and DHCP for Global Unix servers. -Provided 2/3 level support for Incident/Issues with systems. -Managed RedHat ... - 2018 Nov 03
... -Applied Good Manufacturing Principles to be FDA complaint. -Resolve escalated issues as per Service Level Agreements. -Managed DNS, NFS and DHCP for Global Unix servers. -Provided 2/3 level support for Incident/Issues with systems. -Managed RedHat ... - 2018 Nov 03
Customer Service Machine Operator
Bethlehem, PA
... Extensive knowledge in: Project Management, FDA and ISO Regulations, MSDS, Lock out/Tag out, Microsoft Office, Bilingual (Spanish) Education BUSINESS ADMINISTRATION IN PROGRESS MUHLENBERG COLLEGE Major: Business Administration Current GPA: 3.84 N/A ... - 2018 Oct 23
... Extensive knowledge in: Project Management, FDA and ISO Regulations, MSDS, Lock out/Tag out, Microsoft Office, Bilingual (Spanish) Education BUSINESS ADMINISTRATION IN PROGRESS MUHLENBERG COLLEGE Major: Business Administration Current GPA: 3.84 N/A ... - 2018 Oct 23
Supply Chain Medical Device
Douglassville, PA, 19518
... 2014 - 2017 • Designed and led Global data integration and governance program for Trading Partners compliance (NHS, FDA, EU) Arthrex, Inc. • Directed validation of hardware and software for global medical device company Integra Life Sciences. Lead ... - 2018 Oct 11
... 2014 - 2017 • Designed and led Global data integration and governance program for Trading Partners compliance (NHS, FDA, EU) Arthrex, Inc. • Directed validation of hardware and software for global medical device company Integra Life Sciences. Lead ... - 2018 Oct 11
Transportation Planner
Norristown, PA
... All medications shipped thru various channels must meet, and qualify for Federal Guidelines adhered to by the FDA, And Insurance Regulatory Dispatcher /Logistics Coordinator Coca Cola Bottling Consolidated Company - Charlotte, NC November 2004 to ... - 2018 Sep 29
... All medications shipped thru various channels must meet, and qualify for Federal Guidelines adhered to by the FDA, And Insurance Regulatory Dispatcher /Logistics Coordinator Coca Cola Bottling Consolidated Company - Charlotte, NC November 2004 to ... - 2018 Sep 29
Partner Line Manager/Associate Director of Clinical Operations
North Wales, PA
... teams are provided with adequate levels of appropriately qualified resources Leads activities associated with the evaluation, initiation and management of clinical studies to ensure compliance with SOPs, FDA regulations and ICH/GCP guidelines. ... - 2018 Aug 21
... teams are provided with adequate levels of appropriately qualified resources Leads activities associated with the evaluation, initiation and management of clinical studies to ensure compliance with SOPs, FDA regulations and ICH/GCP guidelines. ... - 2018 Aug 21