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Engr , Quality

Job in Franklin Lakes, Bergen County, New Jersey, 07417, USA
Listing for: Kaygen
Full Time position
Listed on 2026-01-12
Job specializations:
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Engr 3, Quality

KAYGEN is an emerging leader in providing top talent for technology-based staffing services. We specialize in providing high-volume contingent staffing, direct hire staffing and project-based solutions to companies worldwide ranging from startups to Fortune 500 and Managed Service Providers (MSP) across a wide variety of industries. The Quality Engineer is accountable for supporting new product development and product maintenance through the application of Quality Engineering skills for medical devices.

This person will handle projects and tasks, from product inception through product launch and maintenance, and play an active role in the process to ensure products meet quality standards consistent with both Corporate and Unit policies, while meeting all design control and other regulatory requirements.

Job Responsibilities:

(Primary Duties, Roles, and/or Authorities)

  • Consistent application of technical principles, theories, concepts, techniques, and quality sciences/tools.
  • Proven problem-solving skills.
  • Makes measurable improvements to Client processes and procedures.
  • Ensures that all design control and production/process control projects meet applicable regulatory (local and international), Corporate, and Unit requirements.
  • Acts as a team member representing Quality on new product development and sustaining engineering projects.
  • Reviews and has Quality Engineering approval authority for new and modified design/process specifications including product performance specification, test methods, etc.
  • Assists with supplier and internal quality system audits as a means of evaluating the effectiveness of the established Quality System and good manufacturing practices (Auditor-in-training).
  • May perform other duties as required.
  • Education and Experience:

    Typically requires a minimum of a bachelor’s degree in science, engineering, or other relevant discipline and a minimum of 5 years relevant experience or a combination of equivalent education and relevant experience.

    Knowledge and

    Skills:

    • Applied knowledge of the FDA medical device quality system regulations and international quality system standards/regulations (e.g. – 21 CFR Part 820, ISO 13485, ISO 14971, MDSAP, EU MDR/IVDR) as it relates to the design and continued support of Client products.
    • Applied knowledge of Corporate and/or Unit requirement.
    • Able to contribute to the completion of specific programs and projects.
    • Can ensure quality conduct of projects, including design, data summary and interpretation, and report generation for self and lower level project developers.
    • Able to revise policies and procedures.
    • Able to make presentations.
    • Can independently determine and develop approach to solutions.
    • Able to provide guidance and work direction to lower level project developers.
    • Can design and perform development working independently within defined parameters with minimal supervision required.
    • Experience with Client software systems utilized in the Quality Systems is desirable.
    • Must have knowledge/specialization in one or more of the following areas:
    • Acceptance sampling theory and application
    • Statistical process control methods and application
    • Measurement system/test method knowledge and analysis
    • Quality planning
    • Failure analysis investigation
    • Design of Experiments
    • Process mapping and value stream analysis
    • Hypothesis testing
    • Descriptive statistics
    • Process capability analysis
    • Basic quality tools:
      Pareto, box plots, histograms, scatter diagrams, etc.
    • Risk Management
    • Supplier quality management
    • Auditing
    • Design/development tools
    • Process validation
    • Software validation

    At KAYGEN, we are always looking for dynamic, talented and experienced individuals. We invite you to join our team of talented IT professionals, consulting at client locations across the globe. Our culture is team‑orientated; we strive to stand by our core values of respect, honesty and integrity. Our team of experienced staffing experts will work with you to find you the best opportunity.

    For more information, please visit us at

    Benefits:
    • Free Healthcare Insurance
    • Vision and Dental Insurance
    • 401(k) Retirement Plan
    • Free Life Insurance
    • Sick Time Off

    Achieve your Kaizen by clicking here. A unique and exclusive talent community supported by Kaygen, that includes programs like:

    • Certifications
    • Mentorship Program
    • Referrals
    • Family and Wellness benefits
    • Continuous Growth and Career Development

    Kaygen

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