Arcadis is the world's leading company in sustainable design, engineering, and consultancy for natural and built assets.
With over 36,000 professionals across 70+ countries, we are united in our mission to improve quality of life and solve the world's most complex challenges.
Job Summary
Our client, a leading provider of medical device technology, is hiring a Quality Engineer on a 12‑month contract.
In this role you will ensure that products and practices meet high quality standards and remain consistent with all relevant requirements.
Responsibilities
Drive c GMP practices within the quality and operations divisions.
Provide support for all relevant quality systems.
Ensure consistent compliance with all internal and external standards and regulations.
Play an active role in the site internal audit team, collaborating closely with auditors.
Prepare and maintain documents to ensure compliance with regulatory requirements.
Support production personnel with continuous improvement activities, such as Six Sigma.
Qualifications
3+ years' experience in a quality position within the medical device or pharmaceutical industry.
A relevant third‑level qualification.
Ability to work on‑site full time.
Why Join Arcadis
At Arcadis, we empower individuals to excel because your contributions matter.
Taking a skills‑based approach, we provide opportunities for you to shape your career, maximize your impact, and grow professionally.
By joining us, you'll engage in meaningful work that drives sustainable solutions for a better planet while leaving a lasting legacy.
Our Commitment to Equality, Diversity, and Inclusion
We are dedicated to creating an environment where everyone can thrive.
Through our six ED&I workstreams—Age, Disability, Faith, Gender, LGBT+, and Race—we foster innovation by bringing together diverse perspectives.
Together, we strive to improve quality of life while building a more inclusive future.
Seniority level
Associate
Employment type
Full‑time
Job function
Medical Equipment Manufacturing
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