Senior Medical Device Regulatory Specialist - Part-Time
Listed on 2026-10-02
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Healthcare
Healthcare Compliance, Medical Device Industry, Medical Science Liaison
Blackrock Neurotech is seeking a Contract Senior Regulatory Affairs Specialist for up to 25 hours per week. The role focuses on regulatory support for medical device programs, ISO 13485/14971 expertise, and developing procedures within the QMS.
It offers flexibility to work remotely or onsite at our Salt Lake City office. Responsibilities include preparing SOPs, evaluating regulatory impact of changes, providing guidance on device development, supporting audits, and maintaining labeling changes
Our organisation is growing, and we are hiring a Senior Medical Device Regulatory Specialist
- Part-Time in United States.
We invite applications for the Senior Medical Device Regulatory Specialist
- Part-Time position located in United States.
The following opportunity is for a Senior Medical Device Regulatory Specialist
- Part-Time with Blackrock Neurotech LLC.
Our team is growing, and we are hiring a Senior Medical Device Regulatory Specialist
- Part-Time in United States.
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