Sr. Quality Engineer

Responsibilities:
Change Control and Design:
Lead the execution of defect management and engineering escalation processes, ensuring timely identification, resolution, and reporting of product issues.
Drive the review and approval of design and service verification and validation protocols, with a focus on product changes and lifecycle processes.
Manage cross-functional teams in product change control processes and ensure comprehensive documentation of product modifications.
Take ownership of maintaining and updating the Device Master Record (DMR) for assigned product lines during post-market changes.
Ensure alignment of design outputs with inputs, proactively addressing discrepancies and ensuring compliance with internal protocols.
Act as the lead liaison between engineering, product management, and quality teams to integrate quality considerations early in the product design phase.
Field, Customer and Safety:
Independently process and triage out-of-box quality issues, conducting root cause analyses and collaborating with teams to drive corrective actions.
Lead post-production safety risk assessments and implement solutions to mitigate safety concerns.
Drive the Medical Device Reporting (MDR) process, coordinating with regulatory bodies and managing field actions and recalls.
Present safety and risk management updates during Safety Risk Management Board Meetings, with responsibility for product-specific risks.
Compliance and Continuous Improvement:
Lead quality improvement projects aimed at optimizing processes, reducing defects, and enhancing customer satisfaction.
Ensure adherence to ISO 9001, ISO 13485, and other relevant regulatory standards, acting as a subject matter expert for compliance.
Implement and analyze quality metrics, creating reports to monitor process performance and drive data-driven improvements.
Conduct internal audits and manage corrective and preventive actions (CAPA) to ensure continued compliance and improvement.
Required Knowledge and Skills:
Advanced knowledge of QMS (Quality Management System) documentation and regulatory standards (ISO 9001, ISO 13485).
Proficiency in quality investigation tools (e.g., Fishbone diagrams, 5 Whys) and statistical analysis (e.g., SPC, Six Sigma).
Understanding of software development lifecycle (SDLC) and experience in defect tracking platforms like Jira
Experience in leading cross-functional teams and managing product changes from initiation through post-market stages.
Strong project management skills and the ability to manage multiple priorities effectively.
Excellent problem-solving, communication, and leadership abilities.
Basic Qualifications:

Bachelor’s degree in Engineering or Science discipline
5+ years in Engineering, Quality or related technical professional experience
Experience in product development and/or maintenance
Experience in process development
Experience working in a regulated environment (i.e. ISO 9001, ISO 13485 or FDA QMSR)
Preferred Qualifications:
Experience working with complex electro-mechanical systems
Experience working with Cloud software and AI/ML
Work Conditions:
Office Environment
May travel up to 25%
Drug Screen: Required
Base Compensation: $80,000.00 to $115,000.00
(Actual compensation is subject to variation due to such factors as location, education, experience, and skillset. We offer a comprehensive benefits package, including medical, dental and vision plans covering eligible US employees and dependents, voluntary wellness and employee assistance programs, life insurance, disability, retirement plans with matching, and paid time off.)
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