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Job Title: Validation Engineer - Routine (West Point) - III (Experienced)
Category:  Professional & Business Operations
•Primary responsibilities for the validation engineer include:
-Day-to-day validation support to manufacturing operations including conducting equipment performance qualifications (specifically cleaning and sterilization validation)
-Authoring validation protocols and final reports, executing validation studies, analysis of validation data
-Resolving technical issues encountered during study execution
-Providing Validation support of manufacturing investigations
•This individual will be required to work in a cross-functional team and independently to accomplish validation objectives
•Off-shift and weekend work may be required 
•B.S./M.S. degree in an engineering/scientific field
•Minimum of 8+ years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry
•Previous experience with cleaning and sterilization validation required
•Proven problem solving/ troubleshooting abilities
•Working knowledge of Microsoft Office products, LIMs, and Trackwise
•Strong technical writing and oral communication skills
•Attention to detail is a must
•Demonstrated ability to work both independently and as a part of a cross-functional team 
Location  West Point , PA
Minimum Experience (yrs):  7+
Required Education:  Not Specified

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