Support implementation of internal quality system requirements and external regulatory standards (e.g., FDA, ISO 13485, cGMP, EU MDR)
Drive improvements to procedures and standards to enhance efficiency while maintaining compliance
Support and coordinate CAPA and compliance programs, including facilitating CAPA activities across functions
Participate in CAPA management activities and global quality system discussions
Conduct internal audits to identify gaps, ensure compliance, and drive continuous improvement
Support audit readiness, including front-room and back-room activities during external audits and inspections
Deliver quality system training and guidance to employees across the site
Lead or participate in system and process improvement initiatives using structured problem-solving approaches
Identify areas of non-compliance and recommend corrective actions to improve overall quality system effectiveness
Provide quality support and oversight for compliance investigations (e.g., non-conformance, OOS/OOT), where applicable
Requirements
Bachelor’s Degree in Science, Engineering, or a related field
2–5 years of experience in a manufacturing environment
Experience in the medical device industry is desirable
Experience in: Non-conformance and CAPA management; Management Review processes; Internal and external audits
Required Skills & Knowledge
Knowledge of ISO 13485, EU MDR, and FDA regulations
Knowledge of cGMP and combination product/device regulations
About Us
As a global medical technology leader for more than 45 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients. If you’re looking to truly make a difference to people both around the world and around the corner, there’s no better place to make it happen.