Twin Cities Quality Assurance Association

Sr. Quality Engineer - Nonin Medical, Plymouth

  • 19 Apr 2017 9:22 AM
    Message # 4763329
    Raja Gollamudi (Administrator)

    Sr. Quality Engineer


    Nonin Medical, Inc. is a rapidly growing international medical device manufacturer that has been designing and distributing high quality medical monitoring devices since 1986.  Headquartered in Plymouth, MN, we offer a rewarding work environment with global opportunities while maintaining a small company, employee-focused atmosphere. 


    The Sr. Quality Engineer plans, coordinates, and directs quality programs and activities to ensure the quality and reliability of Nonin Medical products.  Assure the timely, accurate and independent evaluation of product performance and compliance to safety and regulatory requirements prior to manufacturing and market release.  This role develops, executes and/or monitors quality plans and quality engineering tasks, as well as, manufacturing process validations and controls to ensure compliance with established requirements and regulatory expectations.  The Sr. Quality Engineer provides support for released products, evaluates product field performance and reliability, recommends corrective actions, and plans for continuous improvements.


    Essential Job Functions:

    • Represent Quality in product development teams/projects. Develop & execute plans (quality plan, risk management plan) and requirements (safety, functionality, regulatory, usability) to ensure provisions for quality are addressed and resolved prior to release.
    • Coordinate with the development of essential design control deliverables including, but not limited to product performance analysis on similar products, essential requirements checklist, design verification, design validation, design reviews, phase reviews, and product release authorization for distribution of product.
    • Work closely with Product Development and the project team to develop appropriate verifications, validations (software, process), and qualifications (subcontractors, system and subsystem), for both new design and changes to released product.
    • Review design inputs (specifications) and design outputs (reports, prints, etc.) to assure that appropriate design requirements are specified and to evaluate/confirm quality requirements prior to successful design transfer.
    • Responsible for reviewing, approving and taking ownership of product verification and validation plans and respective test methods.
    • Maintain and serve as a technical expert on EMC standards compliance and testing.
    • Participate in CR/CO process to review and approve engineering change requests.
    • Participate in Material Review Board (MRB) to review and disposition nonconformities and to work with Supplier Quality Engineering to coordinate supplier corrective actions.
    • Work with Manufacturing to direct, coordinate, and monitor production processes to ensure compliance to FDA QSR, ISO 13485, and other applicable regulatory requirements (JPAL, Canada, etc.) and to ensure that safe and effective products are produced.
    • Provide validation support by applying manufacturing quality tools including, but not limited to: FMEA, DFMEA, PFMEA, IQ, OQ, PQ, control plans, process verification/validation plans, Cpk, Cp, SPC, DOE, process data analysis, and DMAIC.
    • Manage complaint investigations, failure analysis of returned products, and issues resulting in a stop ship/stop production; document findings, provide reports and analysis, & document health risk assessment.
    • Compile and institute quality metrics to present at QIT meetings to trend, recommend, and implement corrective actions and appropriate follow-up, when necessary.
    • Lead and manage other, non-product related or continuous improvement projects, as assigned.

    Minimum Qualifications:

                    Required Education and Experience:

    • Bachelors Degree in Electrical Engineering
    • 7 years related experience in Product Development, Manufacturing Engineering and/or Quality Engineering

    Required Knowledge, Skills, & Abilities:

    • Ability to read, analyze, and interpret technical procedures and governmental regulations.
    • Ability to write technical reports, business correspondence, technical procedures, as well as, administrative procedures.
    • Ability to present proposals, data, and issues to Nonin Medical personnel at all levels.
    • Ability to independently determine and develop an approach to a wide range of issues and problems. Solutions must be thorough, practical, and consistent with organization objectives.
    • Ability to represent the department in frequent cross-functional interactions and possible customer, subcontractor, or vendor contacts.
    • Ability to provide solutions to difficult technical issues associated with specific projects.
    • Ability to independently determine and develop technical solutions to a wide range of difficult problems.

    Preferred Qualifications:

    • Experience in product testing and compliance to EMC standards
    • Knowledge of FDA QSR requirements.
    • Knowledge of ISO 13485 and other recognized international quality system standards.
    • Knowledge of world class quality techniques and implementation.
    • Guide the successful completion of major programs and have an ability to perform in a leadership role.

    Physical Requirements:

    • While performing the duties of this job, the employee is regularly required to sit, stand, walk.
    • Must be able to examine assemblies and subassemblies using a microscope.
    • Employee must occasionally lift and/or move up to 50 pounds.
    • On call or after hours support – may be required to support process and design validation efforts during weekends or after work hours.

      Nonin Medical is an Equal Opportunity/Affirmative Action Employer - Minority/Female/Disabled/Veteran.

    Last modified: 28 Jul 2017 3:17 PM | Raja Gollamudi (Administrator)

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