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Equipment Validation Engineer

Job in New York, New York County, New York, 10261, USA
Listing for: Novozen Healthcare LLC
Per diem position
Listed on 2026-02-16
Job specializations:
  • Manufacturing / Production
    Validation Engineer, Quality Engineering
  • Engineering
    Validation Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Location: New York

The Packaging & Assembly Validation team is seeking two experienced Equipment Validation Engineers to support an increased workload across finished goods, packaging, and labeling operations. This is a hands‑on role requiring candidates who can quickly integrate into the team, execute validation activities with minimal onboarding, and adapt to flexible shift requirements in a regulated manufacturing environment.

The ideal candidate will have strong expertise in equipment validation, a solid understanding of quality systems, and demonstrated experience executing IQ, OQ, and PQ activities.

Key Responsibilities
  • Execute equipment qualification and validation activities for:
  • Assembly equipment
  • Packaging systems
  • Labeling equipment
  • Author, review, and execute IQ, OQ, and PQ protocols
  • Perform risk assessments and support commissioning activities
  • Support validation efforts across finished goods manufacturing operations
  • Prepare and maintain validation documentation, including:
  • Protocols
  • Qualification reports
  • Work within established quality systems, supporting:
  • Deviations
  • Investigations
  • Quality-related documentation
  • Collaborate cross‑functionally with Manufacturing, Quality, and Engineering teams
  • Demonstrate flexibility with shift schedules, including occasional weekend support as required
Required Qualifications
  • Hands‑on experience in Equipment Validation
  • Proven experience supporting finished goods, packaging, and labeling operations
  • Strong working knowledge of IQ, OQ, and PQ execution
  • Experience with risk assessments and equipment commissioning
  • Solid understanding of quality systems, including deviations and quality control processes
  • Ability to work independently and execute qualification activities with minimal training or supervision
  • Adaptable, flexible, and comfortable working in a fast‑paced, regulated manufacturing environment
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