SonicJobs Logo
Login
Left arrow iconBack to search

Quality Engineer

Gold Group
Posted a day ago, valid for 18 days
Location

Crawley, West Sussex RH10, England

Salary

£45,000 - £50,000 per annum

Contract type

Full Time

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

Sonic Summary

info
  • The Quality Engineer position involves supporting the local quality management system and processes while advocating for quality within the organization.
  • Candidates are required to have a Bachelor's degree in engineering or a related field, along with relevant experience in quality, regulatory, or engineering roles, preferably in the medical device sector.
  • The role includes responsibilities such as analyzing process data, preparing monthly metrics, and participating in external audits before regulatory authorities.
  • Strong communication skills, the ability to work independently, and a structured approach to problem-solving are essential for success in this position.
  • The salary for this role is competitive, and candidates should have a minimum of 3-5 years of experience in a similar role.

Quality Engineer

As a Quality Engineer, you will support the local quality management system and processes. You will act as an advocate of Quality and promotes the group's vision and mission while supporting the goals of the overall business. You will work closely with functional teams in areas such as, Supplier Quality, Manufacturing ,Order fulfilment, and Regulatory Affairs, among others.

Responsibilities

  • Work on projects / compliance activities to completion.
  • Prepare monthly metrics for their area of expertise / responsibility.
  • Analyze process data and trends and drives optimization / improvement.
  • Represent QA organization in specific processes (e.g. CAPA, Order fulfillment, Manufacturing, Deviation management etc.)
  • Support others in the QA organization and other functional organizations on technical aspects to drive results.
  • Participate in external audits before regulatory authorities.
  • Promote and maintain adherence to company values.
  • Preparation of Internal audit plans, execution of audits and preparation of audit reports as applicable.

Required skills and experience

  • Bachelor's degree in engineering or equivalent or a related field or a formal engineering apprenticeship with demonstrated experience in a similar role
  • Training and experience in relevant medical device regulatory requirements and standards (e.g. ISO, IEC, MDR, MDSAP.)
  • Lead audit trained in ISO13485/9001
  • Proven experience in relevant areas of Quality, Regulatory or Engineering, preferably within a medical device environment.
  • Strong written and verbal communication skills and ability to collaborate effectively as part of a team.
  • Objective driven and customer focused.
  • Capable of producing results working unsupervised under own initiative.
  • Professional integrity. Able to translate regulations into meaningful business requirements.
  • Possess a structured approach to problem solving with an appreciation of quality tools & techniques.

Services advertised by Gold Group are those of an Agency and/or an Employment Business.
We will contact you within the next 14 days if you are selected for interview. For a copy of our privacy policy please visit our website.

Apply now in a few quick clicks

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.