Staff Auditor, Quality System Compliance & Audit (Hybrid - Acton, MA)

We are seeking a seasoned and strategic Staff Internal Quality Auditor to join our Quality Compliance & Audit team under the global Quality Systems organization. This role is critical to ensuring the integrity and continuous improvement of our Quality Management System (QMS). The ideal candidate will bring 8–10 years of experience in Quality Assurance or Regulatory Affairs within the medical device industry, with expertise in auditing, regulatory compliance, and quality systems leadership. Reporting to the Director of Quality Systems Compliance & Audit, the Staff Auditor owns, drives, and leads multiple quality system processes, including Internal/External Audit and Inspection, Corrective and Preventive Action (CAPA), Risk Management, and Metrics & Reporting.

Key Responsibilities

• Lead the planning, execution, and reporting of complex internal audits across global sites in accordance with Insulet requirements, applicable international regulations and standards including ISO 13485, 21 CFR Part 820, EU MDR 2017/745, and the MDSAP approach.
• Develop, maintain, and execute a robust, risk-based, internal audit program that proactively identifies compliance risks and drives continuous improvement.
• Serve as a key liaison and subject matter expert during external audits, including FDA inspections, Notified Body audits, and other regulatory authority engagements.
• Lead cross-functional teams supporting external audits including preparation, back-room management, issue tracking, and driving follow-up activities.
• Oversee audit responses including root cause analysis and ensure timely and effective implementation of CAPAs resulting from audit findings.
• Collaborate with global quality, regulatory, and other internal risk control teams to harmonize audit practices and ensure consistent compliance across the organization.
• Analyze audit data, identify trends, and present findings to management and/or regulatory bodies in support of the audit process, which may include coaching process owners and key stakeholders on compliance gaps, data, and/or resulting corrective actions.
• Design, develop, and facilitate training programs to enhance organizational understanding of quality system requirements, audit preparedness, and regulatory compliance.
• Influence key cross-functional stakeholders to adopt quality improvements and act as a catalyst for organizational change.
• Author and present high-impact presentations and executive summaries to senior management.
• Oversight and management of the internal guest auditor program
• Mentor and train junior auditors and cross-functional teams on audit readiness, regulatory expectations, and quality system best practices.
• Partner with key stakeholders to support the development, implementation and continuous improvement of the established risk-based QMS and process-approach.
• Create and/or improve quality systems to ensure best practices are utilized including conducting assessments, write and execute quality plans, manage change.
• Regularly advise key stakeholders and management on ways to improve quality system effectiveness, with emphasis on preventive action.
• Review procedures to ensure compliance with applicable regulatory and corporate standards
• Perform additional duties as part of the Quality Systems team as required
  
  

Education And Experience

• Bachelor’s degree in engineering, life sciences, or a related technical discipline; advanced degree preferred.
• 8–10 years of experience in Quality Assurance or Regulatory Affairs in the medical device industry.
• Extensive functional knowledge of ISO 13485, 21 CFR 820, EU MDR 2017/745, MDSAP, and global regulatory requirements.
• Demonstrated success leading internal audits and managing external regulatory inspections.
• Strong command of audit, CAPA processes, risk management, and quality system controls with ability to educate others.
• Exceptional attention to detail with the ability to manage multiple high-priority projects in a fast-paced environment.
• Excellent written and verbal communication skills, including experience presenting to executive leadership.
• Proven ability to influence and lead cross-functional teams and drive change.
• High level of integrity, professionalism, and strategic/risk-based thinking.
  
  

Required Skills/Competencies

• CQA, CMDA, or equivalent active certification
• Ability to inspire and motivate cross-functional teams by building trust through active engagement, delivering impactful coaching and feedback, and fostering a culture of accountability and continuous improvement.
• Strategic mindset with a proactive approach to identifying and mitigating compliance risks.
• Strong analytical and problem-solving skills with a focus on root cause and sustainable solutions.
• Effective communicator with the ability to tailor messaging to diverse audiences, including executive leadership.
• Working with various digital business platforms and eQMS tools (LMS, LIMS, PLM, ERP, etc.)
  
  

Preferred Skills/Competencies

• Expert user skills in the M365 Office suite including Teams, and SharePoint
• Experience with electronic QMS solutions and audit management tools
• Familiarity with additional international regulatory frameworks (e.g., Health Canada, TGA, PMDA)
• Experience with PLM tools such as Agile and/or Arena
  
  

Job Type: Full-time

Travel: Minimal, up to 20%

NOTE: This position is eligible for hybrid working arrangements and requires on-site work from an Insulet office.

Additional Information

Compensation & Benefits: For U.S.-based positions only, the annual base salary range for this role is $112,425.00 - $168,637.50 This position may also be eligible for incentive compensation. We offer a comprehensive benefits package, including:

• Medical, dental, and vision insurance
• 401(k) with company match
• Paid time off (PTO)
• And additional employee wellness programs Application Details: This job posting will remain open until the position is filled. To apply, please visit the Insulet Careers site and submit your application online. Actual pay depends on skills, experience, and education.
  
  

Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet’s flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com.

We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!

At Insulet Corporation all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

(Know Your Rights)