*Position: Sr. Validation Analyst *

*Location: Hampton, NJ *

*Duration: 2 months (6-8 weeks) and extendable*

*Locals or nearby face to face*

* *

*SAP exp with be huge plus *

* *

*Background Qualifications:*

·        5+ years experience in a regulated environment (pharmaceutical is
required, medical device is desirable).

·        5+ years in a computer systems validation role.

·        Project management experience.

·        Proven computer validation expertise.

·        Excellent technical writing and presentation skills.

·        Strong analytical and problem solving skills

·        Demonstrable knowledge of the pharmaceutical industry and
applicable regulations.

·        Direct experience with key systems: Document Management,
Laboratory Systems, Project Management Systems, Clinical Trial Management
Systems, Clinical Data Management Systems, Quality Tracking Systems,
Regulatory Information Systems, etc. preferred

·        Knowledge and experience in the maintenance and use of
manufacturing systems, especially in a regulated environment.

·        Knowledge and experience in the maintenance and use of scientific
systems, especially in a regulated environment.

·        Experience in the validation of manufacturing, laboratory and
clinical applications as well as quality systems.

·        Self-motivated with the ability to work independently.  Requires
minimal supervision to set and achieve goals.

·        Some travel required.



Thanks & Regards

Nanda Lakkakula

Vertigon Consulting Inc.
Phone: 201-786-2670 Fax: 732-398-0506
Email: na...@vertigonconsulting.com, URL: www.vertigonconsulting.com

YIM: nanda9848075057

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