Hello, Hope you are doing great,
Please go through the below job description and let me know if you are interested in this position. If yes, please send your updated resume with contact details and best pay rate ASAP. *Location: Hopewell, NJ * *Duration: 6 months* *Title: Validation Specialist - Senior* *Category* *Name* *Required* *Importance* *Level* *Last Used* *Experience* Specialties Quality Assurance Yes 1 Advanced Yes 6-10 yrs Specialties Tester Yes 1 Advanced Yes 6-10 yrs Technical Test Scripts Yes 1 Advanced Yes 6-10 yrs Additional Skills required: Test Lead Test Planning (System Test and UAT) Test case writing (system and UAT) System Test case execution UAT coordination Reviewing SOPs and training material ELN and or LIMS validation experience 6+ years experience • Apply FDA, MHRA, and other applicable global regulations to the development of computer systems supporting regulated business processes • Follow SOPs and industry best practices • Conduct training on good documentation and good testing practices • Facilitate the Computer system Validation Risk Assessment to identify governing regulations and validation deliverables during the development of the computer system • Review validation deliverables for projects which are contracted to third party suppliers • Maintain close communication with stakeholders and team members to keep apprised of computerized system needs, impacts on computer validation, project validation status, and other relevant issues • Assist in planning, implementing, and documenting user acceptance testing • Review computerized systems validation documents such as: o Requirements Specification o Design Specification o CSV Risk Assessment o Test Plans o Test Summary Reports o Data Migration Plan o Pre/Post Executed Test Scripts o Traceability Matrix o Release to Production Statements • Direct and review testing • Provide guidance on quality issues that affect the integrity of the data or the system • Prepare validation summary and test summary reports • Obtain and respond to QA review • Participate in establishing standard quality and validation practices • Independently assess compliance practices and recommend corrective actions • Approve validated computer system related change requests • Monitor regulatory and inspection trends and advise the business on suitable action If you are interested in this position please respond with *updated résumé, rate and Contact details ASAP*. Reply to va...@sureitinc.com<http://us.mc374.mail.yahoo.com/mc/compose?to=va...@sureitinc.com> or call me on 602-334-4209 -- Please ADD MY *Yahoo IM: krishnavarma09* ** Thanks, Best Regards, Varma Sure IT Solutions Inc. 1801 W Queen Creek RD | Suite # 3 | Chandler | AZ 85248 Phone:602-334-4209 FAX: 866-322-0121 Email: va...@sureitinc.com, varma.sur...@gmail.com http:/www.sureitinc.com http://www.linkedin.com/in/krishvarma Arizona. (The contents of this e-mail are confidential to the ordinary user of the e-mail address to which it was addressed and may also be privileged. If the reader of this message is not the intended recipient, any dissemination, distribution or copying of the information contained in this Internet message is strictly prohibited. If you have received this e-mail in error please notify us by telephone or e-mail the sender by replying to this message, and then delete the e-mail and other copies of it from your computer system. Thank you. We believe this email to be virus free but do not warrant that this is the case and we will not accept liability for any losses arising from any virus being transmitted unintentionally by us.) --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "zilliontechnologies" group. To post to this group, send email to zilliontechnologies@googlegroups.com To unsubscribe from this group, send email to zilliontechnologies+unsubscr...@googlegroups.com For more options, visit this group at http://groups.google.com/group/zilliontechnologies?hl=en -~----------~----~----~----~------~----~------~--~---
