Quality Systems Engineer

About this opportunity

About the role: Boston Scientific was recognized by Forbes as one of the Best Workplaces for Engineers in 2026, reflecting a culture where engineers do meaningful work. Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day. Are you passionate about quality, compliance and continuous improvement? Would you like to use your expertise to help 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'll take ownership of key quality system processes, work closely with cross-functional teams and help drive improvements that support product quality and patient safety. Work model, sponsorship, relocation: At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time. 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, 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, supporting 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.