We use cookies. Find out more about it here. By continuing to browse this site you are agreeing to our use of cookies.
#alert
Back to search results
New

Regulatory Quality Engineer

Spectraforce Technologies
United States, California, Santa Clara
Jul 15, 2026
Title: Regulatory Quality Engineer

Duration: 12 Months

Location: Santa Clara, CA 95054

Description / Summary:

This role will provide quality system and compliance support to the Regulatory Affairs (RA) organization by -

  • Driving preparation of KPI dashboards and maintaining a pulse on formal RA management review and internal metrics.
  • Managing strategic program for RA audit preparedness including anticipatory identification of risks, mitigation of risks identified during the audit process, and preventive actions for risks.
  • Investigating non-conformances (e.g., CAPAs), implementing mitigations, and monitoring effectiveness of CAPAs.
  • Identifying and implementing system and/or systemic processes.
  • Supporting tracking and maintenance of regulatory post-approval commitments.
  • Driving quality system process improvement initiatives.


Initiatives include but are not limited to:

1. Establishing audit risk mitigation activities for critical RA tasks.

2. Improving and maintaining quality system procedures (e.g., change management).

3. Liaising with cross-functional partners and international affiliates to meet compliance needs and driving to implementation/resolution.

4. Participating in audit backrooms, and / or front rooms, and

5. Participating in RA projects.

Exposure to Medical Device US and CE regulations, Quality Systems, a Quality role, or a Compliance role is a must.

List of tasks:

  • Develop and implement an "auditing plan" for critical RA tasks (e.g., mock audits for Technical Files/Technical Documentations, Impact Assessments, Archival) as part of audit risk mitigation activities.
  • CAPAs/Auding Finding management.
  • Key Performance Indicator results / metrics management
  • Change management (change orders for procedural updates)
  • Post-Approval Regulatory Commitments management
  • Support QMS audits from an RA perspective
  • Support QMS Integration tasks


Skills:

  • Independent
  • Troubleshooting
  • Critical thinker
  • Communication and Collaboration
  • Ability to drive a problem through resolution and implement mitigations.
  • Ability to handle multiple streams simultaneously with timely execution.


Experience:

5 - 7 years
Applied = 0

(web-77cf7d65c7-jdxdg)