Hi , Hope you are doing great!!!
Please send resumes to *[email protected] <[email protected]>* 1. Sr Validation Engineer with Biovia 2. Sr Validation Engineer Document Management *Skills: Validation, 21 CFR PART 11* JD : • Significant experience in Quality and Compliance with substantial hands-on computer system validation experience • Experience in FDA regulated environment with good understanding of GxP related processes including Risk Based validation • Experience with Change Control processes • • Knowledge of FDA guidance’s and industry standards (e.g. GAMP, Quality & Compliance, FDA regulations & international regulations (e.g. 21 CFR Part 11, Part 820, Annex 11)) • Experience with Change Control processes • Hands on experience in HP Quality Center and QTP • Strong verbal and written communication skills • Able to work as a team player, lead a team or accomplish tasks without supervision. • Ability to work with remote teams and support several changes/projects simultaneously. *Thanks & Regards*, Vinay Genuineit LLC *Certified Women Owned Business* (832 539 3475 **[email protected] <[email protected]>* **[email protected] <[email protected]>* **[email protected] <[email protected]>* *http://in.linkedin.com/pub/vinay-b/a1/401/734/ <http://in.linkedin.com/pub/vinay-b/a1/401/734/>* *GTalk id:[email protected] <id%[email protected]>* -- You received this message because you are subscribed to the Google Groups "mainframe" 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/mainframe. For more options, visit https://groups.google.com/d/optout.
