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Quality Design Engineer

  • Ubicación:

    Galway, Irlanda

  • Contacto:

    Nigel O'Callaghan

  • Tipo de trabajo:

    Permanent

  • Teléfono de contacto:

    +353 21 485 7209

  • Industrias:

    Medical Device & Diagnostics

  • Correo de contacto:

    nigel_ocallaghan@oxfordcorp.com

Are you interested in progressing your career with a global leader in medical devices? Are you ready to challenge yourself in a fast-paced, highly-regulated environment? Are you an experienced Quality Engineer with technical expertise in pharmaceutical or medical device environments? You could be the perfect candidate for this opportunity! Don't hesitate, apply today!

Job Description

You will be fulfilling the QA responsibilities for new product development and post market (commercial product) support, including:

  • Improving patient safety, customer satisfaction and product quality.
  • Understanding and complying to quality, business, health & safety systems and market/legal regulations governing the quality systems.
  • Removing or mitigating against risks associated with the design, use and manufacture of medical devices.
  • Ensuring commitment to training requirements and understanding and complying with all required regulations.


Key Responsibilities

  • Interface with R&D, Regulatory Affairs, Clinical, Medical Safety, Complaints Management Centres and Post Market Quality Assurance team environment providing technical and quality systems input.
  • Familiarity with requirements and procedures that govern medical device Design Control
  • Represent the function for area of responsibility in both Internal and regulated Authority Audits
  • Understanding of Design Assurance requirements to ensure new product/technology transfers comply to all internal and regulatory requirements.
  • Identify and resolve complex exceptions to work assignments.
  • Seek to support improvements in product and process quality.
  • Provides both quality and technical input to ongoing product development and post market commercial product activities.


Key Requirements

  • HETAC Level 8 (240 credits) in a STEM discipline with a minimum of 2-4 years' experience in a similar role.
  • Experienced in risk management, design and process change, standards compliance (to regulatory requirements).
  • Practical knowledge of 13485 and FDA part 820.
  • Good technical capabilities, communication skills, teamwork abilities and initiative.
  • Proven ability to work well as part of a team & on own with minimum supervision


Benefits

  • Competitive and attractive employee compensation package
  • Pension contributions
  • Health insurance
  • Paid holidays


Location: Galway | Ireland