Quality Engineer

1970-01-01Davis Companieshttp://daviscos.com/wp-content/themes/davis_theme/assets/images/logo.svg325 Donald J. Lynch Boulevard, Suite 201MarlboroughMA01752USAcustomer support[+800-482-9494][+508-481-8519]
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Quality Engineer

  • Specialty:

    Engineering
    • City:

      Dover
    • State:

      NH
    • 03820
  • Assignment Type:

    Direct Hire
  • Job Id:

    48062

Description

We are looking for a Quality Engineer to join our client in Dover, NH on a direct hire basis. 

The Quality Engineer is responsible for activities related to the quality and regulatory compliance to the Quality Management System and external medical device quality/regulatory bodies. The Quality Engineer plays a key role in the manufacture and distribution of products. This position reports directly to the Quality Manager.

 

Essential Functions:
  • Develop, document and implement QA Procedures as needed.
  • Responsible for products within a given therapy line (Design to Product Release)
  • Ensures that suppliers deliver quality parts, materials, and services.
  • Helps qualify suppliers according to company standards and may assist with supplier audits as needed.
  • Maintains risk management files for products within a given therapy line
  • Interpret and assess conformity to appropriate regulatory standards.
  • Analyze non-conforming materials and returned goods and recommend disposition and corrective actions.
  • Create suitable data analysis tables and report findings based on statistical evidence and trending.
  • Provide analytical investigations and develop root cause for non-conformances and deviations.
  • Design and specify gauging and test equipment for quality assurance functions.
  • Analyze data and generate summary reports.
  • Interface with vendors and customers as required.
  • Review documentation for completeness and accuracy.
  • Independently develops qualification and validation protocols/reports.
  • Complete other tasks as assigned by the Quality Manager.
  • Collaborate with quality, production engineering and manufacturing teams to establish quality standards for new and existing products.
  • Participates in design reviews, risk management, validations, CAPA’s, NCMR’s, etc.
  • Assures the content of Design History File meets regulatory and company requirements.
  • Develop and manage metrics for product reviews, quality management reviews, contract manufacturer oversight and other quality data.
  • Support planning and execution of design verification, validation, and risk management reviews.
  • Support process qualification and verification.

 

Education and Experience:

  • BS or MS in Engineering, or scientific disciple with 3+ (MS) or 5+ (BS)  years of experience in the manufacture of medical devices/disposables for the medical device market.
  • Medical Device industry experience required; preferably in vascular access.
  • Experience working with remote suppliers and facilities, both domestic and international - preferred
  • Certified Quality Auditor or Certified Biomedical Auditor (ASQ) – preferred.
  • Clean Room experience – preferred.

 

Knowledge, Skills and Abilities: 

  • Travel up to 25%
  • Knowledge of Sterilization: Ethylene Oxide & Gamma Radiation
  • Team player with strong communication, interpersonal and presentation skills.
  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, drawings and procedure manuals. 
  • Ability to speak and present effectively in a group setting.
  • Ability to write routine reports and correspondence.
  • Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry.  Ability to apply concepts such as fractions, percentages, ratios and proportions to practical situations.
  • Ability to problem solve.
  • Must possess a strong attention to detail.
  • Must have a strong computer literacy.
  • Expert understanding of GMP, quality systems, ISO 13485 and FDA QSR for medical devices.
  • Knowledge of standards applicable to Medical Device Safety Risk Management (ISO 14971) & device related compliance standards.
  • Knowledge of Class II medical devices.

Quick Apply

  • As an Equal Employment Opportunity Employer, DAVIS has reporting requirements which require us to invite employees to voluntarily self-identify their race/ethnicity. Submission of this information is voluntary and refusal to provided it will not subject you to any adverse treatment. The information obtained will be kept confidential.
  • Accepted file types: pdf, doc, docx, txt, rtf.
  • By applying to this position and providing my contact information, I give The DAVIS Companies permission to provide me with email communications and information.

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