Celldex Therapeutics-posted 8 months ago
Fall River, MA
Chemical Manufacturing
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The CSV will oversee and coordinate new projects related to validation deliverables and qualifications to ensure existing and new system installations meet all internal and external compliance requirements such as 21 CFR Part 11 and EU GMP requirements throughout the systems development life cycle. This position works on moderately complex problems of diverse scope where analysis of data requires solid evaluation of identifiable factors.
