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Quality Engineer

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1 Vacancy
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Job Location drjobs

London - Canada

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

At Camlon RH we believe that happiness at work comes from the perfect match between the right role the right company the right leader and an environment that truly stimulates you!

We are here to listen understand and get to know the person behind the resume. Our commitment is to present opportunities that will allow you to thrive both professionally and personally.

Are you ready for the Camlon adventure
Our expertise your colors!

Location: London Ontario

Employment Type: Fulltime permanent position

Your Work Environment:

As a Quality Engineer you will play a key role in ensuring compliance with ISO 13485 and FDA regulations managing quality systems and supporting continuous improvement initiatives. You will collaborate with crossfunctional teams to integrate quality into product development supplier management and manufacturing processes while driving regulatory compliance.

Your Daily Responsibilities:

  • Assist in developing and maintaining a robust Quality Management System (QMS) aligned with ISO 13485 and regulatory requirements.
  • Conduct internal audits to ensure compliance and identify areas for improvement.
  • Collaborate with product development teams to integrate quality into design and manufacturing processes.
  • Review design documents and risk assessments ensuring compliance with industry standards.
  • Support supplier evaluations to ensure raw materials and services meet quality expectations.
  • Investigate nonconformances implement corrective and preventive actions (CAPA) and manage resolution processes.
  • Analyze quality data to identify trends and drive continuous improvement initiatives.
  • Oversee customer complaints ensuring appropriate followup and corrective actions.
  • Support training activities to promote quality awareness across the organization.

Your MustHaves:

  • Bachelors degree in Engineering or a related field.
  • Minimum 5 years of experience in medical device quality management systems or a related field.
  • Strong knowledge of ISO 13485 FDA regulations and medical device compliance requirements.
  • Experience with quality analysis tools for problemsolving and continuous improvement.
  • Excellent communication and collaboration skills to work with crossfunctional teams.
  • Strong organizational and problemsolving skills with the ability to prioritize tasks effectively.
  • Ability to work in a fastpaced regulated environment ensuring compliance and quality excellence.

6 Great Reasons to Apply:

  • Competitive salary.
  • Comprehensive insurance program including EAP and telemedicine for you and your family.
  • Companymatched retirement plan.
  • Numerous training coaching and professional development opportunities.
  • A friendly and dynamic work atmosphere with social events sports BBQs and more!

Pssst Looking for a new opportunity but unsure if this one is the right fit

Feel free to send us a spontaneous application at !



Employment Type

Full-Time

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