Quality Engineer II

Boston Scientific • Santa Clarita, CA

277d • $72,800 - $138,300

About The Position

This Quality Engineer II will be primarily supporting a project to relocate sterilization, packaging, and distribution processes and activities from manufacturing sites to sterilization and distribution center locations. This will involve developing, implementing, maintaining and improving quality system elements to ensure a high-quality level of products and processes. Provide guidance and support for other day-to-day activities within the department.

Requirements

• BS/BA Degree in engineering, or a related field.
• 2+ years of experience in quality engineering or related engineering discipline.
• Proficiency in basic Microsoft Office applications (Word, Excel, PowerPoint, Project, Visio).
• Ability to travel up to 10% as needed.

Nice To Haves

• 2+ years of experience in the medical device industry with an understanding of Quality System Requirements.
• Strong technical writing skills and ability to clearly communicate complex information.
• Ability to effectively and efficiently collaborate within cross-functional teams.
• Problem solving experience with nonconformances and/or corrective actions.
• Project/task management experience.

Responsibilities

• Provide Quality Engineering support for sustaining activities and improvement projects for commercial products, with a focus on the project of process relocations within BSC sites.
• Support Non-Conformance Event Prevention (NCEP) and Correction and Preventive Actions (CAPA) activities that include, but not limited to, containment tasks, risk analysis, problem-solving, cause investigations, and written documentation of activities.
• Investigate complaint data, reports, and trends that support projects, issues, and performance of products.
• Participate in project team meetings, contribute to the discussions with questions/feedback, and collaborate with team members to accomplish required project deliverables.
• Review and approve document deliverables in the document approval system. Provide feedback and proposed updates as needed to ensure clear, compliant information.
• Understand, support, and/or drive change assessment strategies.
• Monitor and track the progress of quality-related tasks and initiatives. Collaborate and follow up with team members to ensure completion of assigned tasks within established timelines.
• Communicate across functions and levels to ensure stakeholders are informed and aware of project status, issues, roadblocks, etc.

Benefits

• Compensation for non-exempt (hourly), non-sales roles may include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).
• Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Miscellaneous Manufacturing
• Education Level: Bachelor's degree