| Resume alert | Resumes 71 - 80 of 82 |
Medical Project
Providence, RI
... Committee on Pulmonary Artery Catheterization and Clinical Outcomes (PACCO), joint committee of NHLBI and Center for Devices and Radiological Health-FDA, 1997. Abstract Reviewer, American College of Chest Physicians, 1998-1999. Study Section, ... - 2012 Oct 15
... Committee on Pulmonary Artery Catheterization and Clinical Outcomes (PACCO), joint committee of NHLBI and Center for Devices and Radiological Health-FDA, 1997. Abstract Reviewer, American College of Chest Physicians, 1998-1999. Study Section, ... - 2012 Oct 15
Medical Manager
Warwick, RI
Patricia Kauffman Email: aboueu@r.postjobfree.com Address: ** **** ****** City: Warwick State: RI Zip: 02888 Country: USA Phone: 401-***-**** Skill Level: Entry Salary Range: 35 Primary Skills/Experience: See Resume Educational Background: See... - 2012 Oct 09
Patricia Kauffman Email: aboueu@r.postjobfree.com Address: ** **** ****** City: Warwick State: RI Zip: 02888 Country: USA Phone: 401-***-**** Skill Level: Entry Salary Range: 35 Primary Skills/Experience: See Resume Educational Background: See... - 2012 Oct 09
Medical Internal Medicine
Providence, RI
... This advisory committee will be responsible for recommending the changes for pregnancy labeling for all FDA approved drugs. st 2000 Edited, Medical Care of the Pregnant Patient, 1 edition. (700 pgs) ACP-ASIM. Richard V. Lee, M.D., Karen Rosene ... - 2012 Sep 30
... This advisory committee will be responsible for recommending the changes for pregnancy labeling for all FDA approved drugs. st 2000 Edited, Medical Care of the Pregnant Patient, 1 edition. (700 pgs) ACP-ASIM. Richard V. Lee, M.D., Karen Rosene ... - 2012 Sep 30
Quality Assurance Manager
North Providence, RI, 02904
... I have knowledge and experience with FDA, GMP, GR&R, PFMEA, DFMEA, CAPA, "Quality Systems" ISO9000. I have an outstanding interpersonal, organizational and team building skills with a record of improving efficiency, productivity, and profitability ... - 2012 Sep 29
... I have knowledge and experience with FDA, GMP, GR&R, PFMEA, DFMEA, CAPA, "Quality Systems" ISO9000. I have an outstanding interpersonal, organizational and team building skills with a record of improving efficiency, productivity, and profitability ... - 2012 Sep 29
Manager Quality
Somerset, MA, 02724
... confirm expectations and requirements – process validation Achieved business goals working with cross functional teams and staff 2006- 2008 Director of Quality Quality Management Representative for ISO 13485 and FDA regulated audits and activities. ... - 2012 Jul 09
... confirm expectations and requirements – process validation Achieved business goals working with cross functional teams and staff 2006- 2008 Director of Quality Quality Management Representative for ISO 13485 and FDA regulated audits and activities. ... - 2012 Jul 09
Medical Device Project Management
Cumberland, RI
... Regulatory: FDA, DEA, ICH, EMA, OSHA, Six Sigma Quality attributes, Medical Device regulations Process Analytical Technology (PAT), Statistical Process Control, QSR regulations, educational knowledge of regulations of Australia, Japan and India. ... - 2012 May 01
... Regulatory: FDA, DEA, ICH, EMA, OSHA, Six Sigma Quality attributes, Medical Device regulations Process Analytical Technology (PAT), Statistical Process Control, QSR regulations, educational knowledge of regulations of Australia, Japan and India. ... - 2012 May 01
Product Manager
Providence, RI
... As Product Manager I was the company representative to a major medical OEM responsible for all aspects of our relationship including CAPA, CIM, RMA, PPAP, FMEA and compliance to their stringent FDA requirements in addition to all contract ... - 2011 Oct 14
... As Product Manager I was the company representative to a major medical OEM responsible for all aspects of our relationship including CAPA, CIM, RMA, PPAP, FMEA and compliance to their stringent FDA requirements in addition to all contract ... - 2011 Oct 14
Quality/Project Manager
Easton, MA, 02375
... Responsible for ISO13485 Quality Management System in support of FDA regulated Class I and Class II Medical Devices. ● Medical Device experience includes 510K , Device History Files, Risk Management (FMEA‘s & Hazard Analysis), Registrations and ... - 2011 Aug 14
... Responsible for ISO13485 Quality Management System in support of FDA regulated Class I and Class II Medical Devices. ● Medical Device experience includes 510K , Device History Files, Risk Management (FMEA‘s & Hazard Analysis), Registrations and ... - 2011 Aug 14
Project Manager Health
Providence, RI, 02909
... Clinical Research Coordinator, Neuropathic Pain in terminally ill cancer patients Department of Anesthesia (1995-2000) Device and Stem Cell Implant • Wrote IRB study protocol, consent, study documents, generated documentation for FDA submission. ... - 2011 Jul 17
... Clinical Research Coordinator, Neuropathic Pain in terminally ill cancer patients Department of Anesthesia (1995-2000) Device and Stem Cell Implant • Wrote IRB study protocol, consent, study documents, generated documentation for FDA submission. ... - 2011 Jul 17
Research scientist, chemist, manager, cordinator
Johnston, RI, 02919
... problem-solving, data review and interpretation, and multi-tasking Training Analytical Methods Validation – For FDA Compliance, 03/01/10-03/03/10 The Center for Professional Advancement A broad understanding and hands-on knowledge of the ... - 2011 Apr 21
... problem-solving, data review and interpretation, and multi-tasking Training Analytical Methods Validation – For FDA Compliance, 03/01/10-03/03/10 The Center for Professional Advancement A broad understanding and hands-on knowledge of the ... - 2011 Apr 21