Hello, Sunrise Systems Inc is an IT staff augmentation company and a direct vendor for various fortune 1000 clients. Kindly go through the following requirements and send me your resume in word format. Please include your Candidate's complete name, location, availability, rate and contact information in the body of the email along with word copy of the resume.
Please keep the subject line while responding to this email. If you have any more questions, feel free to give me a call. Thanks! -- Sincerely, Dave Karlekar Sunrise Systems [EMAIL PROTECTED] www.sunrisesys.com 732-603-2200 X-216 732-603-2208 (Fax) ------------------------------------------- Job id - PZ30774QMCT Client - Pharma Company Title - Quality Planning & Compliance Reporting Analyst Location - Groton, CT Duration - 3 Months Rate - Open In-person interview is required. Description: QA Tester with experience working in GMP Computer Validation Environment. This is different from the Validation Role. Review and Track the documents - 1000 pages of testing and test scripts Pharma GMP Computer Validation experience is required The Validation QA Consultant, in alignment with the GQO Validation Team, will work to apply global Quality Systems policies and procedures to validation activities for the GDS program. Serves the QM organization as a primary point of contact for quality support requests from the Business & Informatics to ensure that computerized systems are developed & managed in accordance with corporate, regulatory & Informatics standards. . Tasks include writing, revising, and verifying QM deliverables (Quality Planning & Compliance Reporting), reviewing and approval of SLC deliverables (Project planning, requirements and verification). . Contributing to implementation and post implementation planning and monitoring to support effective performance and change management practices. . Provides QA GMP support by reviewing computerized system validation test cases and other quality deliverables as needed. , . Collaborate with business in the creation of validation test cases and documentation. . Knowledge of validation requirements in a GMP environment. . Computerized system validation experience required A minimum of 5 years of GMP validation experience within the Pharmaceutical Industry. The Validation QA Consultant, in alignment with the GQO Validation Team, will work to apply global Quality Systems policies and procedures to validation activities for the GDS program. --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "Embedded_C++_VC++" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [EMAIL PROTECTED] For more options, visit this group at http://groups.google.co.in/group/Embedded_C_VC?hl=en -~----------~----~----~----~------~----~------~--~---
