Associate Quality Assurance Manager

Posted 22 Days Ago
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Carlsbad, CA, USA
In-Office
115K-135K Annually
Senior level
Artificial Intelligence • Healthtech • Analytics
The Role
Support and maintain the Quality Management System (QMS) for compliance with FDA 21 CFR 820, ISO 13485, and MDSAP. Manage CAPA, nonconformance, change control, supplier quality, audits, and investigations. Monitor quality metrics, lead continuous improvement, and partner cross-functionally while providing leadership, training, and support for regulatory inspections and supplier qualification activities.
Summary Generated by Built In

About Carlsmed

Our mission is to improve outcomes and decrease the cost of healthcare for spine surgery. The Carlsmed aprevo® personalized surgery platform is designed to improve the standard of care for spine surgery one patient at a time.

Position Description

The Associate Manager, Quality Assurance supports the development, implementation, and maintenance of the Quality Management System (QMS) to ensure compliance with applicable regulatory requirements and company quality standards. This role will support the Director of Quality Assurance with all quality assurance activities, including document control, audits, CAPA, nonconformance management, and continuous improvement initiatives, while collaborating cross-functionally to support product quality and regulatory compliance. The Associate Manager provides leadership and guidance to quality team members, drives quality objectives, and promotes a culture of quality throughout the organization.


Key Responsibilities

  • Support and maintain the Quality Management System (QMS) to ensure compliance with FDA 21 CFR Part 820, ISO 13485, MDSAP, and other applicable regulatory requirements.
  • Manage quality system processes, including nonconformance management, CAPA, change control, supplier management, trending analysis and quality records.
  • Develop and update processes to improve effectiveness and efficiency.
  • Support internal and external audits, regulatory inspections, and supplier audits, ensuring timely resolution of audit findings.
  • Lead investigations and quality improvement activities, including root cause analysis, corrective and preventive actions (CAPA), and effectiveness verification.
  • Monitor quality metrics and trends, analyze data, and provide recommendations to management to drive continuous improvement and regulatory compliance.
  • Partner with cross-functional teams including Regulatory Affairs, Operations, Manufacturing, Engineering, and Clinical Affairs to support product development, manufacturing, and post-market activities.
  • Provide leadership, coaching, and training to quality personnel and employees on quality system requirements, procedures, and best practices.
  • Support supplier quality and risk management activities, including supplier qualification, performance monitoring, and quality issue resolution as needed.

Qualifications

  • Bachelor degree in Engineering, Life Sciences, Quality Assurance or a related technical discipline or an equivalent combination of education and relevant professional experience
  • 5-8 years of experience in Quality Assurance within a regulated industry
  • Strong working knowledge of ISO 13485, 21 CFR 820 and MDSAP process
  • Direct experience with managing quality system processes such as CAPA, non-conforming products, product release and supplier monitoring
  • Experience in supporting regulatory inspection, internal and external audits
  • ASQ or ISO 13485 lead auditor certification preferred
  • Effective verbal and written communication skills, including the ability to present information to management and auditors.
  • Strong interpersonal and collaboration skills with the ability to work effectively across cross-functional teams.
  • Demonstrated leadership, coaching, and team development capabilities.
  • Proficiency with electronic quality management systems (eQMS), Microsoft Office applications, and quality-related software tools.

Equal Opportunity Employer

Carlsmed is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. Carlsmed is committed to providing reasonable accommodation for candidates with disabilities in our recruitment process. If you need assistance or accommodation due to a disability, please let us know.


Compensation

We are pleased to provide a competitive salary and benefits. Our benefits reflect our investment in the overall health and well-being of our employees and their families, including paying 100% of monthly healthcare, dental and vision insurance premiums, a 401(k) plan with employer matching, and unlimited PTO. The expected pay range is $115,000 - $135,000. Compensation may vary based on related skills, experience, and relevant key attributes.

Skills Required

  • Bachelor degree in Engineering, Life Sciences, Quality Assurance or related technical discipline or equivalent experience
  • 5-8 years of experience in Quality Assurance within a regulated industry
  • Working knowledge of ISO 13485, 21 CFR 820 and MDSAP processes
  • Direct experience managing CAPA, nonconforming products, product release and supplier monitoring
  • Experience supporting regulatory inspections, internal and external audits
  • Experience with document control, change control, trending analysis, and quality records management
  • Leadership, coaching, and team development capabilities
  • Effective verbal and written communication skills, including presenting to management and auditors
  • Proficiency with electronic quality management systems (eQMS), Microsoft Office, and quality-related software tools
  • ASQ or ISO 13485 lead auditor certification
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The Company
HQ: Carlsbad, CA
91 Employees
Year Founded: 2008

What We Do

Carlsmed is a commercial-stage medical technology leader and creator of the personalized spine surgery market with pioneering technology that is transforming spine surgery. The Company has developed the cutting-edge aprevo® Technology Platform that personalizes surgical procedures through a combination of proprietary AI-driven software and patient-specific fusion devices.

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