SQE with 21CFR Part 820, 210, 211 Location: Natick MA Duration: 6+ months
MUST have experience with Medical Deveice - FDA’s regulations such as 21CFR Part 820, 210, 211, 11 and 58 and ISO 13485. Minimum Education and Qualifications · BS degree in software sciences, MS preferred · 5-8 years experience in software system validation in a Medical Device or other FDA regulated environment · Experience will include: Electronic Data Capture, client server applications, PC or network systems, databases and web systems architecture Thanks and Regards, Ram K Vutukuri Pyramid Consulting, Inc. Office: 678-279-7172 Ext. 105 || Fax: 678-935-4466 E-Mail: [email protected]<mailto:[email protected]> || www.pyramidci.com<http://www.pyramidci.com/> || Yahoo IM: ramak77 CMMi Level 3 Certified Offshore center GMSDC- Supplier of the Year (Class IV) - 2008 Deloitte - Technology Fast 50 in Georgia - 2006, 2007 ABC - Georgia Fast 50 Pacesetters Award - 2005, 2006, 2007, 2008 -- You received this message because you are subscribed to the Google Groups "oraapps" group. To post to this group, send email to [email protected]. To unsubscribe from this group, send email to [email protected]. For more options, visit this group at http://groups.google.com/group/oraapps?hl=en.
