| New Role - Quality Specialist Pharma - Onsite @ Lexington, MA at Lexington, Massachusetts, USA |
| Email: [email protected] |
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http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=1530399&uid= Kindly don't send any QA/Tester Profiles, read the JD clearly and share only suitable Profiles. Role: Quality Specialist Location: Lexington, MA Duration: 9+ Months Rate: $50/HR on C2C only (share profiles if you're Ok with this Rate) Implementation Partner: Alku Project: Day to day this person will be routing SOPs thru Veeva, updating plans, managing that entire process start to finish. In addition, part of this role will be managing the records retention room, ensuring integrity of documents, processing requests from the lab. This role will require scanning, filing, being familiar with the Veeva system and occasionally sending off documents to iron mountain. Must Required Skills: - Veeva - Record management - Data integrity - 3 years of pharmaceutical CGMP (Current Good Manufacturing Practice) Thanks & Regards, Rama Krishna K Senior IT Recruiter - US Rudhra Info Solutions 1604 US Highway 130, North Brunswick, NJ-08902 Mail: [email protected] -- Keywords: quality analyst information technology Massachusetts New Jersey New Role - Quality Specialist Pharma - Onsite @ Lexington, MA [email protected] http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=1530399&uid= |
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| 11:43 PM 02-Jul-24 |