Hi ,

Hope you are doing great.!



Please let me know if you are interested for the below requirement .

Please send resume to anil.ku...@stiorg.com or reach me at 609-232-8702



*Details:*

Job title: Validation Engineer

Location: BlvdWoodcliff Lake,NJ

Duration: 12 months



*Job description: *



·         Prepare computer validation documents such as Validation Plans,
User Requirements, Configuration Specifications, Test Protocols, and
Summary Reports. Prepare Change Control documentation.

·         Execute test scripts. Perform risk assessments. Must know 21 CFR
Part 11. Consult on Projects. Prepare Project Plans. BS in a technical
field and 7-10 years’ experience in GxP environment.

·         Provide Leadership to the Validation effort (make sure the right
things are being done)

·         Manage the preparation and approval of (make sure the things
being done a done correctly)

·         Validation documentation deliverables

·         Migration documentation deliverables.

·         Create the content of the validation deliverables

·         Tracking and archiving all documentation deliverables

·         Manage the negotiations of deliverables with CQA

·         Experience in developing test scripts and user acceptance tests
and executing test scripts

·         Experience in developing and writing SOP’s

·         Formulate and compose user training materials, procedure manuals
for implemented systems

*Requirements:*

·         Extensive Pharmaceutical Experience.
7-10 years’ experience in IT Quality Validation in GxP environment. Will
consider less experience.

·         Experience in protocols including IQs/OQs/PQs, project summary
report.
Deep understanding of SDLC and IT/system change management processes.

·         Experienced in writing system implementation project related
documentation such as project charter, implementation plan, communication
plan, risk management plan.
BS degree required. Advanced degree preferred

·         Technical writing experience is a must.
ARISg or another commercial drug safety system exposure/knowledge

·         Experience in validation, pharma industry product saftey systems.

·         This is an upgrade and hosting site changes.
Suppliers: Candidate will be supporting validation for software hosted
internally and externally. Candidate must be familiar with hardware
qualification. Most of the projects are upgrades to systems - some small
and some large.

·         This candidate must be engaged in the projects and understand how
to review proposals, plans and be able to come up with solutions, ideas.
Should be an ""out of the box"" thinker and take initiative.


-------------



*Anil Kumar Software Technology, Inc  Tel: (609)-232-8702*



*Fax: (866) 608-6686 E-mail: anil.ku...@stiorg.com <anil.ku...@stiorg.com>
www.stiorg.com <http://www.stiorg.com/>*

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