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Regulatory Risk Manager Jobs in Preston, ID (NOW HIRING)

Utah State University

Compliance Officer SR

Logan, UT · On-site

... regulatory risk * Oversees or coordinates billing compliance audits and monitoring to evaluate ... Ability to manage multiple complex priorities while exercising sound judgment and discretion.

Utah State University

Compliance Officer SR

Logan, UT · Remote

... regulatory risk * Oversees or coordinates billing compliance audits and monitoring to evaluate ... Ability to manage multiple complex priorities while exercising sound judgment and discretion. Along ...

Flying S Title and Escrow

County Manager

Preston, ID · On-site

Compliance & Risk Management - Ensure adherence to industry regulations and implement risk management procedures. Customer Service - Maintain a customer-centric approach, resolving issues ...

Flying S Title and Escrow

County Manager

Preston, ID · On-site

Compliance & Risk Management - Ensure adherence to industry regulations and implement risk management procedures. Customer Service - Maintain a customer-centric approach, resolving issues ...

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All JobsRegulatory Risk JobsRegulatory Risk Manager JobsRegulatory Risk Manager Jobs in Preston, ID

Regulatory Risk Manager information

See Preston, ID salary details

$50.9K

$103.3K

$169.8K

How much do regulatory risk manager jobs pay per year?

As of Aug 30, 2026, the average yearly pay for regulatory risk manager in Preston, ID is $103,323.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,300.00 and $127,400.00 per year, depending on experience, location, and employer.

What is the difference between Regulatory Risk Manager vs Compliance Analyst?

AspectRegulatory Risk ManagerCompliance Analyst
Required CredentialsBachelor's degree, certifications like CRM or FRM often preferredBachelor's degree, certifications like CCEP or CAMS often preferred
Work EnvironmentFinancial institutions, corporations, regulatory agenciesFinancial firms, healthcare, government agencies
Employer & Industry UsageUsed in banking, finance, insurance sectorsCommon in banking, finance, and corporate compliance
Search & Comparison IntentUnderstanding risk management roles related to regulationsFocus on compliance procedures and regulatory adherence

The Regulatory Risk Manager and Compliance Analyst roles both focus on regulatory adherence but differ in scope. The Regulatory Risk Manager oversees broader risk strategies related to regulations, while the Compliance Analyst concentrates on implementing compliance procedures. Both roles require similar credentials and are prevalent in financial and corporate sectors, but their specific responsibilities and focus areas vary.

Regulatory Risk Manager jobs near you
Infographic showing various Regulatory Risk Manager job openings in Preston, ID as of August 2026, with employment types broken down into 79% Full Time, 20% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $103,323 per year, or $49.7 per hour.

Regulatory Affairs Specialist

Epoch BioSciences

Logan, UT • On-site

Full-time

Re-posted 3 days ago

Job description

Summary

This role is responsible for ensuring that all products comply with applicable global regulatory requirements throughout their lifecycle-from development and registration to post-market surveillance. The Regulatory Affairs Specialist helps ensure regulatory compliance for diagnostics products with FDA, Health Canada, EU, other regulatory bodies, ISO, and business objectives.

Essential Duties and Responsibilities

  • Implement company regulatory affairs procedures.
  • Prepare, compile, and submit regulatory documentation (e.g., 510(k), PMA, CE Technical Files) to global regulatory agencies and with guidance from Regulatory Affairs Manager manage regulatory submissions.
  • Interpret and apply FDA, EU MDR, ISO 13485, and other international regulations to ensure product compliance.
  • Collaborate with cross-functional teams (R&D, Quality, Clinical, Marketing) to support product development and regulatory strategy.
  • Review and approve product labeling, instructions for use (IFUs), and promotional materials for regulatory compliance.
  • Monitor and analyze changes in regulatory requirements and communicate updates to internal stakeholders.
  • Support internal and external audits, including FDA inspections and Notified Body assessments.
  • Maintain regulatory files and databases, ensuring accurate and up-to-date documentation.
  • Participate in post-market surveillance activities, including adverse event reporting and field actions.
  • Provide regulatory input during risk assessments and design control processes.

Qualifications

  • Bachelor's degree in Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field.
  • 2–5 years of experience in regulatory affairs, preferably in the medical device industry.
  • Strong understanding of FDA regulations (21 CFR Part 820), EU MDR, and ISO 13485.
  • Experience with regulatory submissions and product registrations in multiple global markets.
  • Excellent written and verbal communication skills.
  • Strong organizational and project management abilities.

Preferred Qualifications

  • RAC certification (Regulatory Affairs Certification).
  • Experience with electronic submission systems (e.g., eSTAR, EUDAMED).
  • Experience with MDSAP, ISO 14971 (risk management), and clinical evaluation reporting.

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