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.
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