Quality Manager at CAERUS CORP

Blaine, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

31 Jul, 26

Salary

130000.0

Posted On

02 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality management system, FDA 21 CFR Part 820, ISO 13485, CAPA, Complaint handling, Root cause analysis, Risk management, Regulatory compliance, Audit preparation, Nonconformance management, Medical device manufacturing, Process improvement, Leadership, Data analysis, Cross-functional collaboration

Industry

Veterinary

Description

Job DetailsJob Location: Corporate HeadQuarters - Blaine, MN 55449Position Type: Full TimeEducation Level: 4 Year DegreeSalary Range: $90,000.00 - $130,000.00 Salary/yearTravel Percentage: Up to 25%Job Category: ManufacturingWhy Join Us? We’re a mid-sized medical device and contract manufacturer, which means you get the best of both worlds: meaningful work in a regulated environment without the layers of bureaucracy you’ll find at larger organizations. Here, your ideas don’t get lost in an approval chain. Team members are encouraged to provide feedback, share suggestions, and directly see the impact of their work on processes, products, and outcomes. What you contribute matters, and you can see it come to life. Because we’re always growing and evolving, there is a strong opportunity for individuals who enjoy building, improving, and solving problems. If you’re someone who is comfortable rolling up your sleeves, taking ownership, and helping shape how things are done, you’ll thrive here. We do best with people who are curious, hands-on, and motivated to learn and grow. In return, you’ll gain exposure across functions, develop new skills quickly, and have a direct role in improving how we operate. Position Summary: The Quality Manager provides leadership and functional ownership of the Quality Management System (QMS) within a regulated manufacturing environment. This role is responsible for manufacturing and quality operations of Class II medical devices and customer products, ensuring compliance with applicable regulatory requirements, driving continuous improvement, and safeguarding product quality and customer satisfaction. This is a hands-on role requiring direct involvement in CAPA execution, complaint resolution, audit preparation, and quality activities. The position exercises independent judgment and discretion in interpreting quality data, assessing risk, and determining appropriate corrective and preventive actions. Duties and Responsibilities: Provide leadership and functional ownership of the Quality Management System (QMS) within a regulated manufacturing environment, ensuring compliance with FDA, ISO 13485, and other applicable regulatory requirements. Maintain organizational readiness for internal and external regulatory audits and ensure sustained compliance posture, including representation during audits and leadership of audit response and closure activities. Lead the development, implementation, and continuous improvement of quality systems, processes, and standards to ensure operational effectiveness and regulatory compliance. Partner with operations and engineering leadership to resolve complex production quality issues and implement sustainable corrective actions. Own and govern the end-to-end quality system for CAPA and complaints, including prioritization, investigation strategy, root cause analysis, corrective action effectiveness, and closure oversight. Analyze quality data, trends, and systemic issues to drive risk-based decision-making and preventive actions. Provide oversight of supplier quality performance, including escalation and corrective action requirements. Evaluate nonconforming material trends and determine appropriate disposition decisions based on risk and business impact. Provide quality oversight for new product introductions and process changes to ensure compliance and risk mitigation. Collaborate with engineering, manufacturing, and leadership teams to evaluate quality risks and drive resolution strategies. Lead, develop, and support quality personnel by establishing expectations, priorities, and performance standards. Ensure effective execution of quality system requirements across the team and promote accountability and capability development. Align team activities with organizational quality objectives and continuous improvement initiatives. QualificationsMinimum Qualifications: Bachelor’s degree in Engineering, Quality, Life Sciences, or related field (or equivalent experience). 5+ years of progressive quality experience in a regulated manufacturing environment (medical devices strongly preferred). Strong working knowledge of FDA 21 CFR Part 820 and/or ISO 13485 requirements. Direct experience leading CAPA, complaint handling, nonconformance, and audit processes. Demonstrated ability to apply root cause analysis and risk-based thinking to complex quality issues. Proven experience working cross-functionally with engineering, operations, and leadership teams. Experience participating in or leading internal and external regulatory audits Ability to analyze quality trends and drive systemic improvements. Strong communication skills with the ability to influence across functions. What Sets You Apart You take a hands-on approach, take ownership of quality systems and drive issues through resolution. You are comfortable making decisions in a regulated, fast-paced manufacturing environment. You can balance compliance requirements with practical operational execution. You thrive in cross-functional environments and influence outcomes across teams. You focus on long-term system improvement, not just short-term fixes. Compensation: Caerus Corp provides the following information about compensation for this position: Salary Range: $90,000 – $130,000 per year. Benefits: Health, dental, vision, basic life, and AD&D insurance 401(k) retirement plan with employer match Paid time off (Vacation and Protected paid time) and 6 company designated holidays Tuition Assistance Program Employee Brace Program The salary range is based on several factors which will vary based on position. These include labor markets and, in some instances, may include but not limited to education, work experience, scope and responsibilities of position and geographic location. Employment Eligibility / E-Verify: Caerus Corp participates in the federal E-Verify program to confirm the employment eligibility of all newly hired employees. Employment eligibility will be verified after hire through completion of Form I-9 and the E-Verify process, as required by law. Equal Opportunity Employer: Caerus Corp is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by applicable federal, state, or local law. Reasonable Accommodation The Company is committed to providing reasonable accommodation to qualified individuals with disabilities. If you require assistance or accommodation during the application process, please contact talentaquisition@caeruscorp.com. Caerus Corp., headquartered in Blaine, MN is a developer, manufacturer, and marketer of innovative Class II medical devices, medical devices and soft goods. Our brands include: OrthoCor Medical, Red Fox Innovations and New Options Sports.

Responsibilities

The Quality Manager provides leadership and functional ownership of the Quality Management System (QMS) within a regulated medical device manufacturing environment. This role is responsible for ensuring compliance with regulatory standards, managing CAPA and complaint processes, and driving continuous improvement initiatives.