| Resume alert | Resumes 31 - 35 of 35 |
Quality Control Medical
Greenville, NC, 27858
... device trials accurately • Conducted Site Initiation Visits (SIV) with medical staff and PI for site selection • Adhered to all FDA, ICH-GCP, Central and local IRBs, and state laws • Conducted prescreening for patient recruitment before consenting ... - 2012 Jul 20
... device trials accurately • Conducted Site Initiation Visits (SIV) with medical staff and PI for site selection • Adhered to all FDA, ICH-GCP, Central and local IRBs, and state laws • Conducted prescreening for patient recruitment before consenting ... - 2012 Jul 20
Manager Quality
Wilson, NC, 27893
... Manufacturing Practices in Biomanufacturing Processes (BTEC Capstone Course) Course focused on many areas that included: FDA regulations, ICH Q7A, enforcement, SOPs, quality control, documentation and records, validation, buildings and facilities ... - 2010 Jun 17
... Manufacturing Practices in Biomanufacturing Processes (BTEC Capstone Course) Course focused on many areas that included: FDA regulations, ICH Q7A, enforcement, SOPs, quality control, documentation and records, validation, buildings and facilities ... - 2010 Jun 17
Project Manager Engineering
Wilson, NC, 27893
... Leader of final development of process/facilities/equipment for launch of new Oxycodone HCl formulation (FDA approved in April 2010) . Directed engineering and facilities for Tech Transfer of Naloxone- based antagonist product to U.S. location. ... - 2010 Jun 12
... Leader of final development of process/facilities/equipment for launch of new Oxycodone HCl formulation (FDA approved in April 2010) . Directed engineering and facilities for Tech Transfer of Naloxone- based antagonist product to U.S. location. ... - 2010 Jun 12
Quality Assurance Project Manager
Greenville, NC, 27834
... Generated the Quality integration road-map to ensure current FDA compliance. Directing member of the corporate-wide Computer Compliance Action Team (focused on achieving quality, compliance and validation harmonization & standardization across 8 ... - 2010 Mar 09
... Generated the Quality integration road-map to ensure current FDA compliance. Directing member of the corporate-wide Computer Compliance Action Team (focused on achieving quality, compliance and validation harmonization & standardization across 8 ... - 2010 Mar 09
Quality Assurance Medical Device
Wilson, NC, 27893
... registration with the FDA and directed the regulatory approach for UPG to move from mainly an automotive company into manufacturing Class I and Class II Medical Devices and is working with the Life Science Industry to develop products in these ... - 2010 Mar 09
... registration with the FDA and directed the regulatory approach for UPG to move from mainly an automotive company into manufacturing Class I and Class II Medical Devices and is working with the Life Science Industry to develop products in these ... - 2010 Mar 09