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Design Engineer / Staff Engineer / Product Reviewer

Vacancy Title: Design Engineer / Staff Engineer / Product Reviewer
Contract Type: Permanent
Location: Dublin, Republic of Ireland
Industry:
Salary: Benefits
Start Date: ASAP
REF: J898133_1543857209
Contact Name: Ben George
Contact Email: ben.george@russell-taylor.co.uk
Vacancy Published: 8 days ago

Vacancy Description

Role: Design Engineer / Staff Engineer / Product Reviewer

Location: Dublin / Ireland

Salary: DOE / Excellent Benefits

Russell Taylor Group has a fantastic opportunity for a Design Engineer / Staff Engineer / Product Reviewer to join our client's location in Ireland, Dublin. Due to the ongoing growth and success, we are searching for an experienced Medical Device Assessor who will join our leading Medical Regulatory Team and working with limited supervision, will independently plan and carry out complex and high-level (often of a highly confidential nature) projects to achieve our company objectives.

Responsibilities:

  • Performs needs analysis to identify areas for study or opportunities for new programs.
  • Resolves technical issues and explains client's procedures and requirements.
  • Coordinates complex laboratory activities by developing data sheets
  • Have a strong customer focus, flexibility subject to training and qualification milestones, perform key CE certification responsibilities to support safe products to market.
  • Resolves complex engineering issues associated with Variation Notices
  • Represents our clients on technical committees of national and/or international organizations.
  • Provides leadership and technical advice on special projects that involve complex, new or unusual issues
  • May provide direction as a Primary Designated Engineer or Designated Engineer for specific product categories.

Skills:

Degree in Microbiology, Biochemistry, Electrical or Mechanical Engineering or equivalent experience

Competent working knowledge of ISO 13485 and relevant medical device directive (MDD)

Technical knowledge of the design / manufacturing of medical devices in line with ISO 13485

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h r @ r u s s e l l - t a y l o r . c o . u k