| Resume alert | Resumes 51 - 60 of 213 |
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
Manager Engineering
Pennsburg, PA
... I transitioned from engineering testing to engineering design to engineering management to program management(project management) to manufacturing to process improvement to quality assurance (ISO, FDA). While in my Operations roles, I have applied ... - 2018 Jul 30
... I transitioned from engineering testing to engineering design to engineering management to program management(project management) to manufacturing to process improvement to quality assurance (ISO, FDA). While in my Operations roles, I have applied ... - 2018 Jul 30
Quality Engineer Mechanical
Hatfield, PA, 19440
... Carries a proven track record of success in identifying and implementing operational cost savings and productivity improvements while maintaining adherence to strict regulatory standards for FDA and ISO. Excels in directing and leading teams in ... - 2018 Jun 27
... Carries a proven track record of success in identifying and implementing operational cost savings and productivity improvements while maintaining adherence to strict regulatory standards for FDA and ISO. Excels in directing and leading teams in ... - 2018 Jun 27