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Manager, Quality & Regulatory Compliance

Teladoc Health


Job Location:

Goleta, CA - USA

Monthly Salary: $ 140000 - 150000
Posted: 26 July 2026 (30+ days ago)
Application Deadline: 23 October 2026
Vacancies: 1 Vacancy

Job Summary

Join the team leading the next evolution of virtual care.

At Teladoc Health you are empowered to bring your true self to work while helping millions of people live their healthiest lives.

Here you will be part of a high-performance culture where colleagues embrace challenges drive transformative solutions and create opportunities for growth. Together were transforming how better health happens.

Summary of Position

The Manager Quality & Regulatory Compliance oversees the Quality Management System (QMS) and ensures compliance with applicable quality and regulatory requirements. This role partners cross-functionally to support ISO 13485 compliance audits supplier quality CAPA risk management product development post-market activities and regulatory submissions.

Essential Duties and Responsibilities

Quality Systems & Compliance

  • Maintain and improve the QMS in compliance with ISO 13485 and applicable regulations.

  • Manage document control SOPs training quality records and management reviews.

  • Coordinate internal external and certification audits.

  • Monitor quality metrics and drive continuous improvement initiatives.

  • Lead CAPA processes root cause investigations and corrective actions.

Supplier Quality

  • Manage supplier qualification audits and Approved Supplier List activities.

  • Support supplier performance monitoring investigations and corrective actions.

  • Review supplier changes and assess quality and regulatory impact.

Complaint Handling & Post-Market Surveillance

  • Oversee complaint investigations trending adverse event reporting and post-market surveillance activities.

  • Identify quality signals and ensure appropriate escalation and risk management actions.

Risk Management & Product Development

  • Maintain product risk management documentation throughout the product lifecycle.

  • Support design control product development verification validation and change management activities.

  • Ensure quality and regulatory requirements are integrated into development processes.

Regulatory Affairs

  • Develop regulatory strategies and support product registrations submissions approvals and licenses.

  • Maintain technical documentation and regulatory compliance in global markets including CE Marking activities.

  • Review product labeling marketing materials and promotional claims for compliance.

Audits & Operational Quality

  • Support regulatory inspections product audits and ISO 13485 certification audits.

  • Drive operational quality improvements nonconformance investigations process validation inspections calibration and training activities.

Qualifications Expected for Position

  • Bachelors degree in Engineering Quality Regulatory Affairs Life Sciences or related field.

  • 7 years of experience in medical devices healthcare technology or another regulated industry.

  • Experience with ISO 13485 or similar quality management systems.

  • Knowledge of CAPA audits supplier quality complaint handling risk management and design controls.

  • Strong project management organizational and communication skills.

Preferred Qualifications

  • ASQ certification and/or Lead Auditor certification.

  • Experience supporting regulatory inspections and certification audits.

The base salary range for this position is$140000 - $150000. In addition to a base salary this position is eligible for a performance bonus and benefits (subject to eligibility requirements) listed here: Teladoc Health Benefits 2026.Total compensation is based on several factors including but not limited to type of position location education level work experience and information is applicable for all full-time positions.

We follow a Flexible Vacation Policy intended for rest relaxation and personal time. All time off must be approved by your manager prior to use. You will also receive 80 hours of Paid Sick Safe and Caregiver Leave annually. This applies to full-time positions only. If you are applying for a part-time role your recruiter can provide additional details.

As part of our hiring process we verify identity and credentials conduct interviews (live or video) and screen for fraud or misrepresentation. Applicants who falsify information will be disqualified.

Teladoc Health will not sponsor or transfer employment work visas for this position. Applicants must be currently authorized to work in the United States without the need for visa sponsorship now or in the future.

Why join Teladoc Health

As an Equal Opportunity Employer we never have and never will discriminate against any job candidate or employee due to age race religion color ethnicity national origin gender gender identity/expression sexual orientation membership in an employee organization medical condition family history genetic information veteran status marital status parental status or pregnancy). In our innovative and inclusive workplace we prohibit discrimination and harassment of any kind.

Teladoc Health respects your privacy and is committed to maintaining the confidentiality and security of your personal furtherance of your employment relationship with Teladoc Health we collect personal information responsibly and in accordance with applicable data privacy laws including but not limited to the California Consumer Privacy Act (CCPA). Personal information is defined as: Any information or set of information relating to you including (a) all information that identifies you or could reasonably be used to identify you and (b) all information that any applicable law treats as personal information. Teladoc Healths Notice of Privacy Practices for U.S. Employees Personal information is available at this link.


Required Experience:

Manager


About Company

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