| Resume alert | Resumes 21 - 30 of 42 |
Engineer Project Manager
Peoria, IL
... Extensive knowledge of biological and pharmaceutical principles and techniques: Genetic Engineering, DNA transformation, isolation, amplification, and purification, FDA Regulations, Quality Control, Clinical Trials, Adverse drug reactions, and ... - 2012 Sep 29
... Extensive knowledge of biological and pharmaceutical principles and techniques: Genetic Engineering, DNA transformation, isolation, amplification, and purification, FDA Regulations, Quality Control, Clinical Trials, Adverse drug reactions, and ... - 2012 Sep 29
Medical Quality Assurance
Gurnee, IL, 60031
... • Experience with IRB submissions, Informed Consents, and FDA regulations. • Experience in regulatory processing of Research Clinical Trials. • Experience with enrolling patients, informed consents, and reporting adverse effects for clinical trial ... - 2012 May 11
... • Experience with IRB submissions, Informed Consents, and FDA regulations. • Experience in regulatory processing of Research Clinical Trials. • Experience with enrolling patients, informed consents, and reporting adverse effects for clinical trial ... - 2012 May 11
Medical Data Entry
Lombard, IL, 60148
... Have extensive understanding of FDA and IRB regulations and operations. Experience in investigator initiated as well as industry sponsored research. My key skills include very detail oriented, enthusiastic, team worker and able to lead. I have ... - 2012 Apr 20
... Have extensive understanding of FDA and IRB regulations and operations. Experience in investigator initiated as well as industry sponsored research. My key skills include very detail oriented, enthusiastic, team worker and able to lead. I have ... - 2012 Apr 20
Project Manager Process
bourbonnais, IL, 60914
... 8+ years specialized experience in validation • Developed documentation for Type C meeting with FDA • Participate on large global team to support technology transfer project • Support the development and implementation of novel approaches to solving ... - 2012 Apr 18
... 8+ years specialized experience in validation • Developed documentation for Type C meeting with FDA • Participate on large global team to support technology transfer project • Support the development and implementation of novel approaches to solving ... - 2012 Apr 18
Executive Assistant, Management
Alton, IL, 62002
... LOUIS, MO 1991 - 2002 Executive Assistant to Vice President of Nutrition Science 1991 –1998 • Participated as team member in submission of FDA petition resulting in soy protein health claim. Received DuPont Marketing Excellence Recognition. • ... - 2012 Apr 09
... LOUIS, MO 1991 - 2002 Executive Assistant to Vice President of Nutrition Science 1991 –1998 • Participated as team member in submission of FDA petition resulting in soy protein health claim. Received DuPont Marketing Excellence Recognition. • ... - 2012 Apr 09
Customer Service Medical
Waukegan, IL, 60085
... Additionally accomplished following: • Documentation of complaints to insure compliance with Operating Procedures and FDA regulations • Established and maintained active communication with vendors, sales and marketing • Involved in redlining CELL ... - 2012 Apr 05
... Additionally accomplished following: • Documentation of complaints to insure compliance with Operating Procedures and FDA regulations • Established and maintained active communication with vendors, sales and marketing • Involved in redlining CELL ... - 2012 Apr 05
Manager Quality Control
Oak Lawn, IL, 60453
... as well as ISO 9000 standards • Maintaining HACCP standards • Practice of GLP and cGMP in a pharmaceutical, food, and FDA setting • GC-MS/FID • Aseptic technique • FTIR • Experience with USDA and FDA guidelines • UPLC/HPLC • LC/MS • Exactive ... - 2012 Apr 05
... as well as ISO 9000 standards • Maintaining HACCP standards • Practice of GLP and cGMP in a pharmaceutical, food, and FDA setting • GC-MS/FID • Aseptic technique • FTIR • Experience with USDA and FDA guidelines • UPLC/HPLC • LC/MS • Exactive ... - 2012 Apr 05
Project Manager
Wauconda, IL, 60084
... Sponsored by the FDA/NIH. VOLUNTEERING Volunteer Advocacy Project (Middle TN) Summer 2010- January 2011 Vanderbilt University Kennedy Center for Research on Human Development Nashville, TN Completed training Projected to serve up to four families ... - 2012 Mar 28
... Sponsored by the FDA/NIH. VOLUNTEERING Volunteer Advocacy Project (Middle TN) Summer 2010- January 2011 Vanderbilt University Kennedy Center for Research on Human Development Nashville, TN Completed training Projected to serve up to four families ... - 2012 Mar 28
Technician Manager
Park Ridge, IL, 60068
... Provided daily documentation as required by DOT, FDA, JACHO, Human Resource. 07/08-09/08 Rehab Tech, Inc, Burr Ridge, IL - Rehab Repair Technician Job description and duties transferred with sale of Apria’s Rehab Division. 09/07-07/08 Apria ... - 2012 Mar 26
... Provided daily documentation as required by DOT, FDA, JACHO, Human Resource. 07/08-09/08 Rehab Tech, Inc, Burr Ridge, IL - Rehab Repair Technician Job description and duties transferred with sale of Apria’s Rehab Division. 09/07-07/08 Apria ... - 2012 Mar 26
Analytical Scientist III, EHS Advisor
Columbia, IL, 62236
... • Developed anti-nerve agents for allied military forces, with specific formulations and component design requirements conforming to FDA, BP, and JP regulations. • Conducted EHS audits and compliance reports for laboratory and formulation ... - 2012 Mar 16
... • Developed anti-nerve agents for allied military forces, with specific formulations and component design requirements conforming to FDA, BP, and JP regulations. • Conducted EHS audits and compliance reports for laboratory and formulation ... - 2012 Mar 16