Senior Quality Supervisor

Senior Quality Supervisor

Work mode: Onsite

Onsite Location(s): Maple Grove, MN, US, 55311

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

Responsible for providing leadership to a team of Quality Engineers and Technicians that directly support production in ADSA (Access & Delivery Solutions Assembly) Business Unit. This role will ensure a high level of product & process quality, meeting ISO and regulatory requirements, monitoring key performance indicators, and data analysis for continuous improvement activities.

You will be required to have a sound understanding of the Quality Management System to ensure compliance and assist in troubleshooting quality issues as they arise. In addition, you will be expected to partner with other leaders within the organization to develop business strategy and implement quality strategic initiatives and improvements that will meet or exceed internal and external requirements.

At Boston Scientific, we value collaboration and synergy. This role follows an onsite work model requiring employees to be in our local office five days per week.

Relocation assistance is not available for this position at this time. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

Your Responsibilities Will Include:

• Provides leadership to champion departmental or cross-functional initiatives.
• Provides direction, coaching, and mentoring to engineering team personnel.
• Provides technical guidance in identifying and resolving quality issues using engineering essentials and other related problem-solving tools and techniques.
• Partners with cross-functional teams to ensure quality objectives are met and to provide solutions to quality issues and customer complaints.
• Works closely with business partners to establish project priorities.
• Identifies and implements effective systems and process controls supporting the development, qualification, testing, measurement, or ongoing manufacturing of products.
• Monitors key quality performance indicators of the team and reprioritizes project work in order to meet established objectives.
• Proactively investigates, identifies, and implements best-in-class quality practices.
• Focuses on continuous improvement by championing value improvement projects (VIP) and lean business practices (LBP).
• Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

Required Qualifications

• Bachelor's degree with an Engineering or Science background.
• 4+ years of experience in quality/operations or equivalent.
• 2+ years of direct or indirect leadership experience.
• Demonstrated effective change leadership.
• Demonstrated achieving established goals.
• Demonstrated problem-solving capabilities.
• Strong business acumen and communication skills, with the ability to quickly establish impact and consequences.
• Ability to collaborate and influence across multiple, cross-functional teams.

Preferred Qualifications

• 2-3 years of supervisory experience.
• Understanding and working knowledge of Medical Device Quality Systems and Regulatory Requirements.
• Experience in Medical Device industry.