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 <609-454-0103>*

*as...@atikatech.com <as...@atikatech.com>*

*http://www.atikatech.com <http://www.atikatech.com/>*

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