Quality Systems Engineer III

The Quality Systems Engineer III supports the Global Quality Systems and Acquisition Integration team within the Document and Records Control function. This role provides global process and digital system support, partnering with IT and cross-functional stakeholders to maintain compliance, support continuous improvement and ensure effective quality system performance. The position contributes to the development, maintenance and enhancement of quality system processes and tools that support compliant information lifecycle management across Boston Scientific.

At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model and requires the employee to work from a local Boston Scientific office at least three days per week. Eligible locations include the United States (Marlborough, MA; Arden Hills or Maple Grove, MN; or Dorado, PR), Israel (Yokneam or Yokneam Lumenis), Costa Rica (Global Hub), Ireland (Galway, Cork, or Clonmel), and Canada (Mississauga).

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.

• Execute assigned process ownership responsibilities within a global governance framework while collaborating with global process stewards who provide compliance oversight.
• Support standardization efforts and maintain audit readiness in accordance with applicable regulations and standards, including ISO 13485, 21 CFR Part 820 and EU MDR.
• Participate in process monitoring, documentation updates, regulatory implementation activities and issue resolution to maintain a permanent state of compliance.

• Serve as a quality systems subject matter expert and business partner for digital platforms supporting document and records control processes.
• Collaborate with IT and cross-functional stakeholders to support system configuration, enhancements, issue resolution and lifecycle management activities.
• Partner with IT to translate business and regulatory requirements into technical solutions, validation activities and testing strategies.
• Support root cause investigations, incident management and timely resolution of system-related issues to minimize business disruption.

• Support continuous improvement initiatives using structured methodologies, including VIP, to drive efficiency, scalability and operational excellence.
• Identify, analyze and resolve quality system issues using systematic problem-solving methodologies, considering common practice or procedures.
• Drive process enhancements that strengthen quality culture and improve overall system effectiveness.

• Serve as an owner or contributor for nonconformance, exception and CAPA activities.
• Support root cause analysis, corrective and preventive action planning, implementation and effectiveness verification.
• Contribute to risk management activities and systemic issue resolution efforts.

• Support global quality system projects, including process implementations, business transfers and acquisition integrations.
• Contribute to the global quality systems roadmap and support alignment with organizational commitments and priorities.
• Participate actively in Communities of Practice activities to promote standardization and adoption of best practices.

• Support external audits and regulatory inspections through preparation, execution, back-room…