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Validation Engineer

Job in North Reading, Middlesex County, Massachusetts, 01889, USA
Listing for: 3B Staffing
Full Time position
Listed on 2026-06-17
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing, Validation Engineer, Pharma Engineer, Quality Engineering
Job Description & How to Apply Below
  • Must be local ALREADY in the MA area
  • 3-7 years of experience in pharmaceutical or biopharmaceutical manufacturing validation
  • Direct experience authoring and executing equipment qualification protocols (DQ/IQ/OQ/PQ)
  • Solid working knowledge of FDA cGMP regulations (21 CFR Parts 210/211) and GMP documentation standards
  • Experience writing and managing GMP documentation - protocols, reports, SOPs, batch records
  • Demonstrated project management capability - Gantt ownership, milestone tracking, and cross-functional coordination in a technical environment
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