Thread View: sci.bio.herp
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Started by http://biotech.fyicenter.com
Tue, 04 Nov 2008 16:50
US-AZ-Tempe: Biocompatibility Engineer
Author: http://biotech.fyicenter.com
Date: Tue, 04 Nov 2008 16:50
Date: Tue, 04 Nov 2008 16:50
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4241 bytes
US-AZ-Tempe: Biocompatibility Engineer To apply for this position, please visit this Website. http://biotech.fyicenter.com/jobs/99894175_Biocompatibility_Engineer.html To see other BioTech job opportunities, please visit http://biotech.fyicenter.com/ Date: 04-Nov-2008 Biocompatibility Engineer Overview: This position is responsible for assessing material changes and understanding biologic, polymeric, and metallic delivery materials and implants, and for identifying the appropriate biocompatibility testing for new materials. Responsibilities: 1. Works independently and/or within a team to develop and assess issues related to the development of new or improved medical products. 2. Recommends material testing using NMR, IR, DSC, ESCA, SEM, GPC, and HPLC techniques. 3. Implements laboratory procedures and policies relating to new material assessments and their biocompatibility. 4. Provides timely information to product teams on material issues which will affect the new product development. 5. Prepares technical presentation relevant to material technologies. 6. Assesses biocompatibility and aging test requirements for new products. 7. Functions as a team member on product development teams. Qualifications: Ph.D. in Materials Science or M.S. in Materials Science with 5 years experience within the medical device or closely related industry. 1. Ability to concurrently handle a variety of projects. 2. Ability to independently work with in-house and outside industry/academia to maximize scientific outcomes. 3. Ability to independently work with outside medical and technical professionals. 4. Skills in communicating with all levels of technical and operating management. 4. Knowledgeable in problem solving concepts. 5. Ability to generate test protocols and reports. 6. Comprehensive understanding of regulatory environment (FDA and ISO 10993). 7. Comprehensive understanding of GMP and GLP requirements. 8. Ability to understand toxicological assessments. 9. Strong knowledge of material/tissue/ blood interactions. 10. Strong knowledge of common surface and analytical analyses techiniques. 11. Knowledge of software application skills. 12. Knowledge of general medical device process technology. Thank you, BioTech FYI Center http://biotech.fyicenter.com/
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