Kindly Send Resumes to a...@vertigonconsulting.com
Position: Quality Validation Analyst Location: Andover, MA Duration: 6+ months *Locals or nearby Face to face must * Provide technical writing support for IT Quality Management activities As a document coordinator, organize, standardize and maintain workflow of documents for validation documentation structure including change control Provide technical writing abilities for developing controlled documents involved with new computer systems implementations, change controls and other deliverables of computer systems validation. Develop documentation to capture User Requirements, Functional Requirements, Design Documents, IQ/OQ/PQ Test Scripts, Validation Plans and Summary reports, system manuals, SOPs, etc. in an efficient manner. Must have good working knowledge of 21 CFR Part 11. Maintain reporting data on Key Performance Indicators (KPI’s) regarding Computer System Validation Statistics Support communication between the members of IT and other departments *Qualifications:* BA/BS degree preferred or equivalent pharmaceutical industry experience required. 3-5 years experience in writing GxP computer systems validation documentation in a pharmaceutical or research environment. Must have working experience in 21 CFR Part 11 Must be able to work with minimal supervision Computer skills including MS Word, Excel, PowerPoint and Lotus Notes Must be able to function in a team environment Excellent written skills Excellent communication and interpersonal skills Thanks & Regards Adem Technical Recruiter Vertigon Consulting Phone: 201-786-2670 Fax: 732-398-0506 Email: a...@vertigonconsulting.com URL: www.vertigonconsulting.com IM: adem_verti...@yahoo.com -- You received this message because you are subscribed to the Google Groups "it req" group. To post to this group, send email to it-req@googlegroups.com. To unsubscribe from this group, send email to it-req+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/it-req?hl=en.
