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Resumes 51 - 60 of 107 |
Pittsburgh, PA
... product photography, TV commercial design Design of marketing 'call sheet', eCommerce and weekly SEO discussions Support of our FDA clinical trials and study support with independent labs Selection of testing labs for medical products research and ...
- 2015 May 28
Pittsburgh, PA
... modeling/drafting (finite element analysis (FEA) and computational fluid dynamics (CFD)) Gained experience with facets of FDA quality system regulations with emphasis on Design Controls (21 CFR 820.30), human factors analysis, formulation of ...
- 2015 Mar 22
Bethel Park, PA
... QUALIFICATIONS • Six Sigma Greenbelt Certified Minitab • Certified IPC 610 Specialist • Knowledge and experience with FDA 21 CFR 820, ISO 9001, IEC 60601, ISO 13485, Lean Manufacturing, 5S, Electrostatic Discharge safety • Experience writing and ...
- 2015 Feb 25
Pittsburgh, PA
... Expanded in large scale and characterized the cord blood T cells in GMP environment for a planned clinical trial to adoptively infuse the expanded CBT cells to patients after cord blood transplantation (submited to FDA as investigational new drug ...
- 2014 Jun 02
New Kensington, PA
... Tested Medical devices using Labview (level 8.5) to determine acceptance for the FDA . Tested devices using Windaq, a data acquisition tool measuring time/amplitude (for data cleansing) . Software: Word, Excel, Outlook (and Paint to edit jpg files ...
- 2014 Mar 22
Pittsburgh, PA
... • Worked in the flow cytometry core facility under FDA and NIH guidelines and regulations and • supervised several graduate students and core facility technicians. Member of International Society of Analytical Cytometry. • ! ! PROFESSIONAL ...
- 2014 Jan 27
Pittsburgh, PA
... Durham, NC ● Discovered unmet clinical needs to develop business cases and surgical solutions for medical devices by working with surgeons and researching applicable markets, patents and FDA regulations ● Collaboratively created conceptual designs ...
- 2014 Jan 23
Washington, PA
... Ensured adherence to FDA Good Manufacturing Practices. Supervisor - Powder Metallurgy Lab, 6/1992-8/1993 Supervised ten union employees in the application of ti tanium powder coatings on medical components. Developed methods for t racking ...
- 2013 Nov 17
Pittsburgh, PA
... my experience in clinical research to coordinate, monitor and manage all aspects of clinical studies in accordance with ICH Good clinical practices, FDA guidelines, local regulation and the standard operating procedures of your establishment. ...
- 2013 Nov 15
Hampton Township, PA
... Part of the IBM R12 Project team responsible for designing complex customizations in the manufacturing track adhering to the FDA CFR 21 Part 11 norms in GMP validated enviornment, remapping the existing customizations, Complete end to end full cycle ...
- 2013 Oct 23