*Hope you are doing good.*
*Please let me know you have suitable consultants for* *Sr Validation Engineer with Biovia,* *At Foster City, CA* *Please send resume to pa...@clearthougtsolutions.com <pa...@clearthougtsolutions.com>* *Job Description:* Position: Sr Validation Engineer with Biovia Duration: Long term Location: Foster City, CA *1. Sr Validation Engineer with Biovia* *2. Sr Validation Engineer Document Management* *3. Validation, 21 CFR PART 11* *Required Skills* • 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 and Regards,* Pavan Kumar K, Jr IT Recruiter, Clear Thought Solutions LLC., eMail: pa...@clearthoughtsolutions.com, www.clearthoughtsolutions.com Gtalk ID: cts.pavankumar11 -- You received this message because you are subscribed to the Google Groups "oraapps" group. To unsubscribe from this group and stop receiving emails from it, send an email to oraapps+unsubscr...@googlegroups.com. To post to this group, send email to oraapps@googlegroups.com. Visit this group at http://groups.google.com/group/oraapps. For more options, visit https://groups.google.com/d/optout.
