About the Job
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
At the company, we provide the opportunity to work with a diverse and high-performing team dedicated to tackling significant health industry challenges. With access to the latest tools, information, and training, we support your career advancement and skills development. You will find an environment that encourages progressing your ambitions.
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Quality Systems Engineer – 12-Month Fixed-Term Contract
About The Role
The company has been recognized by Forbes as one of the Best Workplaces for Engineers in 2026 and as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, showcasing our meaningful work culture.
Are you passionate about quality, compliance, and continuous improvement? Do you want to utilize your expertise to ensure that life-changing medical devices meet the highest quality standards? Join our Quality team at the European Distribution Center as a Quality Systems Engineer on a 12-month fixed-term contract. In this role, you will take ownership of key quality system processes, collaborate with cross-functional teams, and drive improvements that support product quality and patient safety.
Work Model, Sponsorship, Relocation:
This position follows a hybrid work model requiring employees to be in our local office at least three days per week. At this time, the company will not offer sponsorship or take over sponsorship of an employment visa for this position, and relocation assistance is not available.
Your Responsibilities Will Include
- Maintain and continuously improve our Quality Management System (QMS), ensuring compliance with internal procedures and applicable regulations.
- Manage and improve document control processes to ensure accuracy, consistency, and compliance.
- Act as a quality systems subject matter expert while supporting internal and external audits.
- Identify compliance risks, solve complex quality challenges, and drive practical improvements.
- Partner with cross-functional teams to strengthen quality processes and promote a culture of continuous improvement.
- Provide guidance on quality standards and regulatory requirements to support product quality and patient safety.
Qualifications
Required Qualifications:
- Experience working with quality management systems in a regulated environment.
- Strong knowledge of quality assurance, document control, and regulatory compliance.
- Experience supporting quality system processes, audits, or continuous improvement activities.
- Strong analytical, problem-solving, and communication skills.
- Ability to work independently, take ownership, and collaborate effectively across teams.
Preferred Qualifications:
- Experience in the medical device industry or another highly regulated environment.
- Familiarity with ISO 13485, FDA requirements, and European medical device regulations.
- Experience with electronic document management systems and quality improvement initiatives.
- Experience in a distribution, logistics, or supply chain environment.
