Friday, January 22, 2016

Position: Validation Lead, Richmond, VA

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

ashok@atikatech.com

http://www.atikatech.com

 


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