| Resume alert | Resumes 81 - 90 of 308 |
Registered Nurse Manager
Pottstown, PA
... Well versed with regulatory requirements and reporting timelines for adverse events to FDA, MHRA and EMEA. Comprehensive knowledge in handling Individual Case Safety Reports (ICSR’s). Quick learner who really enjoys new and different challenges. Key ... - 2019 May 01
... Well versed with regulatory requirements and reporting timelines for adverse events to FDA, MHRA and EMEA. Comprehensive knowledge in handling Individual Case Safety Reports (ICSR’s). Quick learner who really enjoys new and different challenges. Key ... - 2019 May 01
Engineering Medical
Chester Springs, PA
... Medical, Exton, PA May - August 2018 Assembled and manufactured devices in clean room in accordance to regulatory guidelines and FDA established protocols, and assisted in lot release and quality control inspections Conducted research and laboratory ... - 2019 Apr 30
... Medical, Exton, PA May - August 2018 Assembled and manufactured devices in clean room in accordance to regulatory guidelines and FDA established protocols, and assisted in lot release and quality control inspections Conducted research and laboratory ... - 2019 Apr 30
Technician Training
Pennsburg, PA
... component level using hand tools, ohm meters and oscilloscopes Extensive record keeping of all serialization forms for the FDA Apply labels to all machine parts and dismantle machines for crating Involved in Kaizen and Daily Management Start-up and ... - 2019 Mar 18
... component level using hand tools, ohm meters and oscilloscopes Extensive record keeping of all serialization forms for the FDA Apply labels to all machine parts and dismantle machines for crating Involved in Kaizen and Daily Management Start-up and ... - 2019 Mar 18
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