***Please no outside agencies or recruiters***
Riverside, located in Eau Claire, WI is a precision machining company. Our company mission is to provide custom precision manufacturing and innovative services to medical, aviation, space, defense, and emerging high-tech industries.
We are seeking a QUALITY MANAGER to join our team! An ideal candidate is a talented leader that is passionate about their work and committed to quality, service, excellence, and innovation.
***This is an ON-SITE position***
Our Culture is best in class!
“Built right. Every time” is not just a slogan. A career at Riverside is rewarding for far more reasons than you might imagine. We build things that make a difference in people’s lives. We understand there are lots of choices out there, that is why for over 40 years we have been providing stability, a safe and clean environment, challenging work and are invested in the growth of our people to take them as far as they want to go. At Riverside, your experience and expertise are highly valued, your contributions are recognized, and your professional goals are supported.
DUTIES AND RESPONSIBILITIES include but not limited to:
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Lead QE implementation of quality planning activities.
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Supports LEAN activities associated with the Quality areas.
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Provides support for all 3rd party audits (FDA, ISO, AS9100 notified body) and customer audits.
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Leads and/or assists with CAPA, Deviations.
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Collaborate on disposition and processing of nonconforming products as a member of the Material Review Board.
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Collaborate with Engineering and Manufacturing on job process planning and improvements.
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Lead Quality Engineers on generation, evaluation, and closure of CAPAs and Non-Conformances including tracking and reporting on corrective action progress. Also work with Quality Engineers on coordination of assigned Corrective and Preventive Actions.
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Act as Management Review representative for the facility, including annual reporting of the quality systems.
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Assess training for inspection departments and other departments on quality requirements.
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Leads all inspection team and departmental meetings.
EDUCATION/EXPERIENCE
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Bachelor's degree or equivalent combination of education and experience. Degree in Engineering, Quality, life sciences or related field preferred.
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Aerospace background is a plus.
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5-7 years’ experience of practical experience in quality assurance and manufacturing engineering; previous work in a medical device environment desired.
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Minimum of 3 years previous supervisory experience; preferably in a manufacturing environment.
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Minimum of 3 years leading and developing quality teams.
KNOWLEDGE/SKILLS/ABILITIES
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Ability to read blueprints.
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Ability to use micrometers, Vernier calipers, and other QA gauges.
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CMM operation or programming is a plus.
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Proficient in Microsoft Office including Word, Excel, Outlook and PowerPoint.
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Strong listening, verbal, and written communication skills.
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Strong ability to multitask, prioritize and adapt to shifting priorities.
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Strong problem solving and decision-making skills and the ability to think independently.
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Familiar with the design controls, FDA regulation, and GMP practices, ISO and AS9100 requirements.
CORE VALUES
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People – We can do it
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Innovation – We work together
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Service – We honor our word
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Quality – We do what’s right