Hi All,
Hope you are doing well!!!! Please Send me the suitable profiles to sop...@datagrp.com With rate confirmation Contact Details with Current Location. Position: Sr Validation Analyst Location: Central, NJ (Locals Preferred) Bill Rate: Rate: $60/hr Duration: 6-12+ Months US Citizen or GC/EAD and H1's Pharmaceutical Experience is a MUST! Must have knowledge of Software Validation Life Cycle and the document deliverables associated with the life cycle. This individual must have Quality Assurance experience in the area of review and approval of validation documentation as they pertain to a set of requirements and procedures. Having Maximo experience is a plus. . 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 Thanks & Regards, Sophia Jones Technical Recruiter Data Group, Inc. Certified Minority Women Owned Business Enterprise (MWBE) & Small Business Enterprise (SBE) ________________________________________ |Office: 1 - 732 - 791 - 2348 xtn: 250| Fax: 732 - 907 - 1174 |Email: sop...@datagroupinc.net|Website: www.datagroupinc.net| ________________________________________ Note: Under Bill s.1618 Title III passed by the 105th U.S. Congress this mail cannot be considered Spam as long as we include contact information and a remove link for removal from our mailing list. To be removed from our mailing list reply with "remove" and include your "original email address/addresses" in the subject heading. Include complete address/addresses and/or domain to be removed. We will immediately update accordingly. We apologize for the inconvenience if any caused to you. ________________________________________ --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "REQSRESUMES" group. To post to this group, send email to reqsresumes@googlegroups.com To unsubscribe from this group, send email to reqsresumes+unsubscr...@googlegroups.com For more options, visit this group at http://groups.google.com/group/reqsresumes?hl=en -~----------~----~----~----~------~----~------~--~---
