Hi Partners,
Hope you are doing well.
Please let me know if you have anyone for below mentioned position with resume and following details of your consultant.
Full Name/Phone/Email/Current Location/Availability/Rate
Position: Validation Lead
Location: Richmond, VA
Duration : 6 to 12 months
Job Description:
Experience Required: 8+ years
•Work experience in the FDA regulated Life Science industry.
•Manages computer system validation work, assuring the thoroughness of validation planning and making appropriate progress towards completion of validation work. Write technically sound computer system validation protocols while adhering to company standards and regulatory expectations.
•Perform re-validation(OQ & PQ) and change control validation related activities.
•Acts as liaison between Quality Assurance and the project team to assure that GxP software is implemented in compliance with applicable regulations and guidelines.
•Provides tactical direction and guidance for project teams implementing Computer Systems for new or existing GxP systems including the development and analysis of system requirements.
•Manages all validation aspects of several projects simultaneously.
•Ensure the compliance of computerized systems to regulatory requirements, including but not limited to 21 CFR Parts 210, 211, Part 11 and Eudralex Vol.4 - Annex 11.
Thanks & Regards,
Ashok Kumar
Atika Technologies
5 Independence Way, Suite 300
Princeton, NJ 08540 Direct: 609-454-0103
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