| Resume alert | Resumes 1 - 10 of 550 |
Patient Care Sterile Processing
Lowell, MA
... of customer service, communication skills and professionalism Discuss compliance standards and the role of HIPAA, OSHA, CDC, FDA, ANSI, AAMI, and other regulating agencies Identify central service workflows processes from cleaning, decontamination, ... - Jun 11
... of customer service, communication skills and professionalism Discuss compliance standards and the role of HIPAA, OSHA, CDC, FDA, ANSI, AAMI, and other regulating agencies Identify central service workflows processes from cleaning, decontamination, ... - Jun 11
Clinical Research Internal Medicine
Medford, MA
... IRB approval per regulations (NIH, DHHS,FDA) 2015-18 Committee Member, Disaster Response and Preparedness Committee, ACEP American College of Emergency Physicians, Committee Membership 1998-2008 Founder and CEO of Flights for Humanity, Inc. ... - Jun 07
... IRB approval per regulations (NIH, DHHS,FDA) 2015-18 Committee Member, Disaster Response and Preparedness Committee, ACEP American College of Emergency Physicians, Committee Membership 1998-2008 Founder and CEO of Flights for Humanity, Inc. ... - Jun 07
Supply Chain Inventory Management
Boston, MA, 02210
... Master Data, product definition, product impurity profile, including safety stock, lead times, time fences, aligned to new FDA requirements Supported FTZ implementation and balancing domestic and international storage requirements vs FTZ storage ... - Jun 07
... Master Data, product definition, product impurity profile, including safety stock, lead times, time fences, aligned to new FDA requirements Supported FTZ implementation and balancing domestic and international storage requirements vs FTZ storage ... - Jun 07
Quality Engineer Supplier
Hudson, MA, 01749
... (Printed circuit board assembly, electro-mechanical assembly, and injection molding processes across multiple quality management systems (ISO 9001, 13485, AS9100, FDA CFR 820, DoD). I am currently looking for employment opportunities and open to new ... - Jun 04
... (Printed circuit board assembly, electro-mechanical assembly, and injection molding processes across multiple quality management systems (ISO 9001, 13485, AS9100, FDA CFR 820, DoD). I am currently looking for employment opportunities and open to new ... - Jun 04
Quality Control X-Ray
Newton, MA
... • Illustrated hundreds of significant protein mutations and analyzed them against a panel of FDA approved drugs. • Produced DNA clones of significant mutations to be tested in cell lines. • Docked millions of purchasable compounds against the ... - May 30
... • Illustrated hundreds of significant protein mutations and analyzed them against a panel of FDA approved drugs. • Produced DNA clones of significant mutations to be tested in cell lines. • Docked millions of purchasable compounds against the ... - May 30
Ph D Flow Cytometry
Andover, MA
... Knowledgeable of GxP practices and familiar with ICH, FDA and EMA guidance. Co-travel with the field sales team to provide customer support services. Massachusetts Institute of Technology, Cambridge MA March 2012-Dec 2015 Postdoctoral Fellow Studied ... - May 24
... Knowledgeable of GxP practices and familiar with ICH, FDA and EMA guidance. Co-travel with the field sales team to provide customer support services. Massachusetts Institute of Technology, Cambridge MA March 2012-Dec 2015 Postdoctoral Fellow Studied ... - May 24
Information Technology Project Management
Natick, MA
... Electronic CTD submissions to the FDA. Electronic Lab Notebook. • International project manager for Cisco VOIP deployment. • Vendor management for enterprise applications, infrastructure, data and voice. SLA contractual agreements and negotiations. ... - Apr 23
... Electronic CTD submissions to the FDA. Electronic Lab Notebook. • International project manager for Cisco VOIP deployment. • Vendor management for enterprise applications, infrastructure, data and voice. SLA contractual agreements and negotiations. ... - Apr 23
Quality Assurance Clinical Trials
Boston, MA
... Extensive knowledge of pharmacy operations, FDA regulatory affairs, clinical trials of GCP, GMP & GLP, and quality assurance. Proven track record of proper customer advisement and an empathetic attitude towards customers. Superior training and ... - Apr 22
... Extensive knowledge of pharmacy operations, FDA regulatory affairs, clinical trials of GCP, GMP & GLP, and quality assurance. Proven track record of proper customer advisement and an empathetic attitude towards customers. Superior training and ... - Apr 22
Clinical Research Regulatory Affairs
Brookline, MA
... Regulatory Affairs GPA: 4.0/4.0 Relevant Courses: Regulatory Compliance, FDA Pharmaceutical Regulation, Regulatory Strategy for Product development and lifecycle management, Safety sciences, Human experimentation: methodological issues fundamentals. ... - Apr 20
... Regulatory Affairs GPA: 4.0/4.0 Relevant Courses: Regulatory Compliance, FDA Pharmaceutical Regulation, Regulatory Strategy for Product development and lifecycle management, Safety sciences, Human experimentation: methodological issues fundamentals. ... - Apr 20
Drug Safety
Brockton, MA
... Authored company-wide Work Instruction (WI) - Reviewed and processed serious and non-serious product complaints of AEs, including those associated with a medical device, for the FDA, Health Canada and ROW; Initiated and completed the monthly reports ... - Apr 10
... Authored company-wide Work Instruction (WI) - Reviewed and processed serious and non-serious product complaints of AEs, including those associated with a medical device, for the FDA, Health Canada and ROW; Initiated and completed the monthly reports ... - Apr 10