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Quality Control Inspector II

Job in Plainsboro Center, Middlesex County, New Jersey, USA
Listing for: Integra LifeSciences Corporation
Full Time position
Listed on 2026-01-02
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector
Salary/Wage Range or Industry Benchmark: 21.12 - 27.98 USD Hourly USD 21.12 27.98 HOUR
Job Description & How to Apply Below
Location: Plainsboro Center

Changing lives. Building Careers.

Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

Quality Inspector II will be responsible for performing quality assurance inspections on purchased components, manufactured sub‑assemblies and final product. The Quality Inspector will perform all duties in accordance with the requirements of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to be familiar with and able to measure critical dimensions.

ESSENTIAL DUTIES AND RESPONSIBILITIES
  • Perform inspection by using a variety of inspection measuring and test equipment to determine acceptance or rejection of material or parts.
  • Perform first article, incoming/receiving, and in-process inspections of materials or parts; determine acceptance or rejection after inspection and/or testing of materials, parts, and/or equipment.
  • Interpret and work within the guideline of drawings, specifications, charts, procedures, and other data to determine acceptance or rejection of materials.
  • Read and interpret sampling plan as per the American national standard institute (ANSI).
  • Assist in the review and disposition of non‑conforming material and customer returned material, including rework, scrap, and return to vendor.
  • Maintain accurate and current inspection and/or testing records such as, but not limited to, Material Certifications, Inspection/Test Results and reports, Certificates of Conformance, Rejection reports/tags, as required by applicable procedure and/or specification.
  • Coordinate and inform other departments of inspection and/or testing status in support of production and project goals and initiatives.
  • Promote and participate in continuous improvement initiatives.
  • Responsible for the maintenance of appropriate conditions of all quarantine locations.
  • Maintain the QC inspection areas in an orderly fashion conducive to carrying out safe and efficient inspections and procedures.
  • Inspection requirements include training and working in classified clean rooms as necessary to perform in‑process inspections.
  • Maintain records of inspection and all testing performed on the appropriate test records.
  • Perform line clearances and quality reviews in manufacturing, labeling, or other assigned areas during manufacturing activities.
  • Identify and implement opportunities for continuous improvement, including document revisions in order to maintain accurate SOPs.
  • Provide quality support to various departments as needed, e.g. engineering, product development, etc.
  • Assist in training new associates according to the Quality System Regulations and company SOPs as applicable.
  • May also perform other related duties, responsibilities, and special projects as assigned.
DESIRED MINIMUM QUALIFICATIONS
  • Associate degree in science is preferred.
  • 3‑7 years of relevant GMP/GLP experience specific to incoming, line clearance, in‑process, and finished goods inspections in pharmaceutical or medical device industry.
  • QA experience in the medical device industry preferred.
  • Must have strong written and verbal communication skills.
  • Strong organizational skills, self‑directed, strong problem solving and interpersonal skills.
  • Knowledge of CAPA, Validations, Change Control, preferred.
  • Working knowledge of ISO 13485, 21 CFR 820 FDA QSR, and cGMP.
  • Knowledgeable in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) preferred.

Salary Pay Range: $21.12 – $27.98 USD hourly.

Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job‑related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

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