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Quality Control Inspector

Job in Norwood, Norfolk County, Massachusetts, 02062, USA
Listing for: NOVA Biomedical GmbH
Full Time position
Listed on 2026-03-06
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Quality Control / Manager
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Career Opportunities with Nova Biomedical Corporation

Nova Biomedical is an Equal Opportunity Employer in compliance with affirmative action in hiring and promoting women, minorities, veterans, and individuals with disabilities.

Nova Biomedical:
One Global Brand. One Vision. Together under one name.

Advanced Instruments and Nova Biomedical are now united under one brand,
Nova Biomedical
, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we’re accelerating innovation, supporting critical workflows, and delivering world‑class service across the biopharmaceutical and clinical markets.

About the company

At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science‑driven solutions are trusted in over 100 countries to speed drug development and enhance patient care.

Our integration brings together more than 70 years of scientific excellence with Nova’s cutting‑edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA‑registered, ISO‑certified manufacturing, more than 125 FDA approvals, and industry‑trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences.

With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values:
Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity
.

Working at Nova Biomedical means joining a mission‑driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real‑world impact on global health.

The Quality Control Inspector is responsible for inspecting raw materials, assemblies, and finished products using a range of measurement tools and testing software. This role ensures that all products conform to established quality standards, drawings, and specifications. Responsibilities also include documenting inspection results, managing non‑conforming material, and supporting continuous improvement across incoming, in‑process, and final inspection activities.

If you’re passionate about quality control and want to be part of a team that is shaping the future of life sciences, we’d love to hear from you, apply today!

What you’ll do
  • Perform both mechanical and electrical inspections including visual, physical, or functional tests on raw materials and sub‑assemblies to support production.
  • Perform final inspection and operational testing of instruments and review of Device History Records (DHR’s) prior to shipment.
  • Manage and maintain the documentation (electronic and paper), filing, and tracking of incoming inspection reports, as well as non‑conforming material reports (NCMR) for incoming, in‑process, and final inspections.
  • Perform first article inspections to support new suppliers and/or changes to parts.
  • Coordinate and manage calibration activities including record maintenance and scheduling of calibrations.
  • Aid in the maintenance of all Inspection and production records in line with procedures.
  • Promote a culture of quality focused on compliance with customer needs and regulatory requirements.
  • Other duties as assigned.
What we are looking for in you
  • 2–4 years of related experience and/or training, or an equivalent combination of education and experience.
  • Ability to read and write in English.
  • Proficiency with Microsoft Office and comfort learning new software for document control, training, calibration, and ERP systems.
  • Experience in a regulated environment (e.g., medical device, aerospace) preferred.
  • Strong mechanical and electrical aptitude, with the ability to use hand tools and gauges to set up, operate, and troubleshoot related equipment.
  • Associate’s degree (A.A.)…
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