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Validation Engineer Back to search
Contact Information:
Sunrise Systems Inc
PO Box 4647
Metuchen, NJ 08840
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Contact: 
Phone: 
Fax: 
Dave Karlekar
7326032200
732-603-2208

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Reference Number:
PZ27164Validation

Job Description:
Please send resumes at dave@sunrisesys.com with Job id - PZ27164Validation in the subject line
------------------------------------------------------------
Job id - PZ27164Validation
Client - Pharma Company
Title - Validation Engineer
Duration - 2 months
Location - Peapack, NJ
Rate - Open

In Person Meeting is required after phone screening.

Work Schedule is according to project needs
How much OT if any do you predict? 10 hours posibly during execution
Pharmaceutical Experience is required
Pfizer experience is required ? RCS

OVERALL RESPONSIBILITIES:

The Validation Consultant will prepare scripts and perform software, hardware, interface, and data conversion validation studies required to support Pfizer Logistics operations. The scope of this assignment is limited to the RCS validation portion of the Vocollect system installation in Parsippany, which primarily consists of the execution of an RCS IQ and regression testing picking functionality including PTL (Pick to Lights).

MAJOR DUTIES AND RESPONSIBILITIES:

1. Participates in the preparation of all documentation relating to the RCS portion of the Vocollect system installation in Parsippany such as Validation Plans, System Documentation, Qualification Protocols, Test Scripts and Task Reports.
2. Ensures data is properly set up and configured to avoid unnecessary deviations.
3. Executes validation protocols and properly documents tests scripts.
4. Creates appropriate testing scenarios and capable of data manipulation using SQL queries.
5. Documents and communicates to management quality related findings.
QUALIFICATIONS:

BA/BS in Engineering, Computer Science, Logistics, Business or related discipline required. Competency working with Window based PC applications is a must. Experience with AS/400 applications (RCS) is required and EasyPick preferred. A minimum of one year of related experience in the pharmaceutical industry is required. Knowledge of FDA and International Regulations, including current Good Manufacturing Practices, Validation principles, Electronic Record and Electronic Signature regulations, and Good Documentation Practices. Good oral and written communications skills required. Must be able to work flexible hours. Must be able to manage priorities and work with multidisciplinary teams. Excellent analytical, communication, and interpersonal skills required.

Experience Level:
5+ Years

Requirements:

Location:
Bridgewater NJ

Duration:
1 - 3 months

Pay Rate:
DOE

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Date Posted: 01/14/2008
Last Updated: 01/14/2008
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