Quality Control Inspector Review and Release

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.

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, 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
.

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.

• This role is responsible for the completion of the work assigned to you and will contribute to the overall success of the Quality Control (QC) Department.
• Under limited supervision and following established procedures and guidelines, this position supplies assistance and support to the manufacturing operations (consumables or Reagent department areas) and R&D groups.
• You will be self‑motivated and responsible for performing the Real Time Inspection of the Reagent Department filling and packaging, review of Device History Records (DHR), inspection of labels / final products, the performance of line clearances, and possibly the processing of Non‑Conforming Materials in support of Manufacturing’s schedule.
• You will be highly experienced in the inspection of consumables and fluid manufacturing products.
• You will electronically transact product to Finished Goods and will generate and maintain certification for all released products. You will be familiar with retrieving various DHRs per established procedures. You will train other Review & Release Inspectors.

If you’re passionate about [insert relevant part of role] 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!

• Understanding of QSR, GMP, GDP requirements as it relates to assigned responsibilities
• Read and understand APs, TPs, OIs, OPs, drawings, MVs, ECOs, test data and any other documentation in the DHR for the area.
• Correctly scan and file DHR’s and product related information, as needed.
• Perform data entry, as needed
• Final approval of test results and the DHR for product to be released to Finished Goods.
• Perform inspection of documentation revision.
• Will perform visual and/or mechanical inspections on all completed consumable and Reagent Department products
• Will assist in the processing of non‑conforming materials.
• Will generate and maintain certification for reagent products and all consumables for customer use
• Will perform Real Time Inspections in both the Reagent Department and consumables
• Will perform or verify area inspections.
• Communicate to QC group staff and supervisor information to maximize quality and productivity.
• Attend meetings when required.

• List Qualifications/Requirements for role
• Physica…