Hello All, Hope you are doing good.
Send me resumes at <[email protected]> Validation Specialist/Tester with Medical Device Experience *LOCATION: *Philadelphia, PA We're looking for 4-5 experienced CSV specialist/tester resources to fill spots on our large on-site testing team. *REQ. SKILLS* *Perform software verification for a Software as a Medical Device project* Experience with validation of software applications in the medical device industry; Knowledge of GxP; 21 CFR Part 820/ISO 13485 Familiarity with Software Development Life Cycle (SDLC) methodologies and associated CSV deliverables - Validation Plan, URS/FRS, DDS, System and UAT protocols; reports, etc. Hands-on experience with CSV within Johnson & Johnson Operating companies is highly preferable; *Work: *on-site 40hrs week *START DATE: *06/15/2015 *INTERVIEW: **Phone* *DURATION: **6+ months* *Amith* * Sr. Recruitment Manager* *Zenith tech Solutions* * Desk: **518-621-004* <518-621-0048>*6* * Fax: **518-244-4977* <518-244-4977> * 3 park Hill* *Albany, NY 12204* *[email protected]* <[email protected]> -- You received this message because you are subscribed to the Google Groups "Hot List" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/directclienteq. For more options, visit https://groups.google.com/d/optout.
