Base salary + cash-based incentive program; compre...
Bachelor's degree in engineering or related technical field
3 years of experience in quality management
Knowledge of iso 13485, iso 9001, and fda regulations
The primary purpose of this role is to be a functional leader within the quality organization, coordinating team deliverables and providing daily direction to ensure quality requirements are met
Job Summary
The primary purpose of this role is to be a functional leader within the quality organization, coordinating team deliverables and providing daily direction to ensure quality requirements are met.
You will supervise, coach, and direct a team of quality professionals while promoting a diverse and inclusive work environment where team members feel supported and openly communicate opportunities.
The company offers a comprehensive benefits package including immediate eligibility for medical, dental, vision, disability, life insurance, and a 401(k) plan with company matching contributions.
Matching Summary
The primary purpose of this role is to be a functional leader within the quality organization, coordinating team deliverables and providing daily direction to ensure quality requirements are met.
Salary
Base salary and cash-based incentive program; Comprehensive benefits package including medical, dental, vision, disability, life insurance; 401(k) plan with company matching
Skills & Requirements
Must-have
Bachelor's degree in engineering or related technical field
3 years of experience in quality management
Knowledge of ISO 13485, ISO 9001, and FDA regulations
Experience with CAPA and root cause analysis
Ability to lead and develop a team of quality professionals
Nice-to-have
Bias for action and decision making
Strong communication and interpersonal skills
Experience with Manufacturing Excellence culture
Ability to work independently in fast-paced environments
Positive can-do attitude with failure not an option mindset
Key Requirements
Minimum bachelor's degree in engineering or related technical field
Minimum 3 years of relevant experience
Specialized knowledge of EU MDR, ISO 13485, ISO 9001, 21CFR820
Auditing experience required
Technical aptitude for reviewing engineering change requests and nonconformance reports