[REQ ID-7984]{P-R} Validation Engineer // Piscataway, NJ // 6+ Months

Dear Associate,

Hope you are doing well.

I am trying to reach you regarding an opportunity for “Validation Engineer” Position based in “Piscataway, NJ” and the description and Skills required are copied below.

Please revert back to me if you have any Consultants available & interested in below opportunity with word version of your consultant resume, best time & number to contact them along with the hourly rates. Please feel free to contact me to discuss more about this opportunity.

 

 

This is a very high priority and urgent req. Need resumes urgently.

Position            : Validation Engineer

Location           : Piscataway, NJ

Positions          : 2

Start date         : ASAP

Duration           : 6 months

 

Validation Technical Writer/Tester – Life sciences/ Pharma domain is must.

Model-N application is mandatory skill.

 

• Model N's domain-specific solutions and best practices allow manufacturers to enhance price strategy, enforce prices globally, and manage the entire contract life cycle — from offer development to contract compliance — to ensure maximum contract value. Full visibility and control are enabled by powerful reporting capabilities that provide full auditability and analytics that deliver actionable intelligence and deep business insight.

 

• Validation Technical Writer/Tester will have 6+ years of experience in testing or validation of FDA regulated/GxP sensitive systems.
• Well versed with the Validation Testing environment and also the documentation needs for regulatory purpose.
• knowledge of contracting and contract management and the issues related to that area
• Possess excellent documentation skills.
• To author validation test scripts such as URS, SRS, IQ, OQ, PQ on the guidance from the validation manager.
• The candidate should also have served in the role of validation test script quality reviewer (both pre and post execution).
• Additional responsibilities include participating in authoring and review of validation documentation required throughout the testing life cycle including: Requirements documents, Test Plans, Test Summary Reports, and Traceability Matrix.

 

 

 

 

Warm Regards,

 

Bhageerath M

__________________

 

Resource Manager

SYSTEL INC | Atlanta, GA

Office: +1-678-261-5238

Toll Free: +1-888-8SYSTEL (879-7835) x 324

 : Speak2bhageeratha

 

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