Quality Systems Analyst I

Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. About the role Boston Scientific is seeking a Quality Systems Analyst I for a 6-month contract position to support the effectiveness, compliance, and continuous improvement of our Quality Management System (QMS). This is an entry-level opportunity designed for a recent graduate or early-career professional interested in developing experience in Quality within a regulated manufacturing environment. In this role, you will work with experienced Quality team members and cross-functional partners to support quality system activities, maintain quality records, monitor quality metrics, and help ensure activities are completed in accordance with established procedures and applicable quality requirements. The Quality Systems Analyst I will gain exposure to a variety of quality system processes, which may include nonconformance management, corrective and preventive action (CAPA), change control, audits, training, document control, management review, and continuous improvement. This role may also involve supporting quality-related activities with external suppliers, including the collection and monitoring of supplier quality information and performance metrics. The successful candidate will have a strong willingness to learn, good attention to detail, effective communication and organizational skills, and the ability to work collaboratively in a fast-paced environment. At Boston Scientific, we are committed to improving patient lives through innovative medical solutions. This role provides an opportunity to build a strong foundation in Quality Systems while contributing to product quality, patient safety, regulatory compliance, and operational excellence within a global organization. Your responsibilities will include: Support the administration and maintenance of the Quality Management System (QMS). Collect, organize, and analyze quality data and metrics to support monitoring, trending, and continuous improvement activities. Assist with the preparation, review, and revision of quality system procedures, work instructions, forms, and records. Support quality system processes such as management review, document control, and training. Assist with internal, corporate, and regulatory audit preparation and support activities. Learn and apply applicable quality standards, regulatory requirements, and company procedures. Assist with the development, coordination, and maintenance of quality system training materials and records. Assist with monitoring supplier quality information and performance metrics, as required. Participate in quality-related activities associated with projects, process changes, and business improvement initiatives. Participate in continuous improvement activities focused on quality, compliance, efficiency, and risk reduction. Maintain accurate and complete quality records in accordance with established procedures. Complete assigned quality system activities within established timelines and escalate questions or concerns when appropriate. Participate in quality system investigations, problem-solving, and root cause analysis activities under the guidance of experienced Quality team members. Work collaboratively with cross-functional teams including Manufacturing, Operations, Supply Chain, Regulatory Affairs, Design Assurance, R&D, Purchasing, and Operations Quality. Required qualifications: Bachelor’s degree in Science, Engineering, Life Sciences, Quality, Manufacturing, or a related technic…

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