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Remote Fda Jobs in Oregon (NOW HIRING)

Mineralys Therapeutics

Senior Counsel - Compliance

OR · Remote

$262K - $295K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

... remote company. Senior Counsel - Compliance The Senior Director, Compliance will lead the design ... Provide guidance regarding the Anti-Kickback Statute, False Claims Act, Sunshine Act, FDA ...

Care Access

Region Manager

OR · Remote

$95K - $115K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Strong understanding of GCP, FDA regulations, ICH guidelines, and industry best practices required How We Work Together * Location : Remote within the United States. This role requires 100% of work ...

Lumimeds

Healthcare Content Creator (LP/NP/RN/PA/MD)

OR · Remote

Stay current on FDA guidance, GLP-1 research, and compounded medication regulation * Cover topics ... Fully remote, U.S.-based * Time commitment: ~4-10 hours/month, flexible scheduling around shoots ...

ARTHREX

Sr II - Embedded Product Security Engineer (Remote)

OR · On-site +1

$115K - $190K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

REMOTE Title : Sr II - Embedded Product Security Engineer (Remote) Salary Range: Salary Minimum ... Knowledgeable of FDA and ISO guidelines for the development of medical devices required.

Axiom Talent Platform

Life Sciences Attorney (Remote)

OR · On-site +1

$309K/yr

  • Medical

  • Dental

  • Vision

  • PTO

Lead and participate in MLR (Medical, Legal & Regulatory) reviews to ensure promotional content complies with FDA, FTC and other applicable regulations. * Work closely with cross-functional teams ...

micro1 AI

Regulatory Affairs Specialist

Hillsboro, OR · Remote

$50 - $70/hr

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project ... FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to critically read clinical or safety ...

micro1 AI

Biostatistician

Salem, OR · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

micro1 AI

Regulatory Affairs Specialist

Portland, OR · Remote

$50 - $70/hr

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project ... FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to critically read clinical or safety ...

micro1 AI

Biostatistician

Hillsboro, OR · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

micro1 AI

Regulatory Affairs Specialist

Gresham, OR · Remote

$50 - $70/hr

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project ... FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to critically read clinical or safety ...

micro1 AI

Biostatistician

Eugene, OR · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

micro1 AI

Regulatory Affairs Specialist

Beaverton, OR · Remote

$50 - $70/hr

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project ... FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to critically read clinical or safety ...

micro1 AI

Compliance Officers

Beaverton, OR · Remote

$50 - $70/hr

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project ... FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to critically read clinical or safety ...

micro1 AI

Biostatistician

Beaverton, OR · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

micro1 AI

Director of Biostatistics

Bend, OR · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

micro1 AI

Biostatistician

Gresham, OR · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

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Showing results 1-20

All JobsFda JobsRemote Fda JobsRemote Fda Jobs in Oregon

Remote Fda information

See Oregon salary details

$25.9K

$88.4K

$174K

How much do remote fda jobs pay per year?

As of Aug 14, 2026, the average yearly pay for remote fda in Oregon is $88,412.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,366.00 and $114,702.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities of a remote FDA compliance specialist?

A Remote FDA Compliance Specialist generally reviews and updates regulatory documents, conducts virtual audits, and monitors company practices for FDA compliance. They regularly collaborate with cross-functional teams, such as quality assurance, legal, and product development, to provide guidance on regulatory requirements and respond to compliance queries. Additionally, they prepare and submit necessary reports, maintain records for inspections, and stay current on evolving regulations. This remote structure allows flexibility but also demands excellent organization, communication, and self-discipline to ensure all deadlines and compliance standards are met.

What is a remote FDA?

A Remote FDA job typically involves working for or with the U.S. Food and Drug Administration (FDA) from a remote location. These roles can include regulatory affairs, compliance, medical writing, research, and reviewing submissions for drug and medical device approvals. Remote FDA jobs require knowledge of FDA regulations, strong analytical skills, and experience in healthcare, pharmaceuticals, or related fields. They offer flexibility while maintaining high regulatory standards and ensuring public health and safety.

What are the key skills and qualifications needed to thrive in the remote FDA position, and why are they important?

To excel as a Remote FDA Compliance Specialist, you need in-depth knowledge of FDA regulations, quality assurance procedures, and a background in life sciences or a related field. Proficiency in using compliance management systems, electronic document management tools, and relevant certifications such as RAC (Regulatory Affairs Certification) are often required. Exceptional attention to detail, self-motivation, and strong written and verbal communication skills are vital for remote collaboration and thorough documentation. These abilities ensure regulatory adherence, minimize compliance risks, and facilitate effective remote teamwork within the pharmaceutical or medical device industry.

What are the most commonly searched types of Fda jobs in Oregon?

The most popular types of Fda jobs in Oregon are:

What are popular job titles related to Remote Fda jobs in Oregon?

For Remote Fda jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Remote Fda jobs in Oregon look for?

The top searched job categories for Remote Fda jobs in Oregon are:

What cities in Oregon are hiring for Remote Fda jobs?

Cities in Oregon with the most Remote Fda job openings:

Remote Fda jobs near you
Infographic showing various Remote Fda job openings in Oregon as of August 2026, with employment types broken down into 80% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $88,412 per year, or $42.5 per hour.

Director, Regulatory Affairs Advertising and Promotion

Ultragenyx Pharmaceutical

OR • Remote

$149K - $197K/yr

Full-time

Posted 8 days ago

Job description

Position Summary:

ultrafocused - Work together to fearlessly uncover new possibilities

The Director of Regulatory Affairs Ad/Promo will serve as a subject matter expert for regulatory review of advertising and promotional, and non-promotional materials for the U.S. and Canada (CA) and provide regulatory leadership to the Materials Review Committee (MRC) to ensure all communications, advertising and promotional materials and programs throughout the product life cycle are compliant with applicable laws, regulations, and company policies.

Work Model: 

Remote: Officially documented as working full-time from home, with travel to Ultragenyx's offices or other locations on occasion as needed.

Responsibilities:

1. Serve as the MRC Chair and provide direction and regulatory expertise for promotional materials, medical, and payer communications.

2. Serve as primary contact with the FDA (OPDP/APLB) and PAAB as needed, including responding to agency inquiries and managing company requests for advisory review of advertising and promotional material.

3. Review and approve Form FDA-2253 submissions.

4. Provide strategic and operational regulatory guidance on new concepts, campaigns, and product labeling to help ensure promotional materials are aligned with promotional regulations, corporate standards, and policies and business objectives.

5. Support the U.S. and CA commercial and medical teams, by participating in strategy discussions and extended team meetings and providing regulatory guidance and perspective on strategies and objectives and tactics.

6. Maintain current awareness of evolving agency regulations and interpretations, FDA advisory letters, enforcement letters and policy issues and trends affecting the industry; communicate significant changes in Agency perspective to relevant stakeholders.

7. May lead cross-functional process improvements or other special projects.

8. Represent Regulatory Affairs Ad/Promo at regulatory sub-team and labeling meetings; provide strategic regulatory guidance.

9. Other duties as required.

Requirements:

Requires a BA/BS degree; advanced degree preferred (PharmD, PhD, MS, MBA, JD).

2. 10+ years of industry experience including 5+ years of advertising promotion experience.

3. Excellent verbal and written communication skills.

4. Attention to detail and ability to manage multiple priorities simultaneously.

5. Strong interpersonal skills with ability to demonstrate strategic and analytical thinking.

6. Demonstrate and proactively advocate working together in the spirit of transparency that encourages engagement, collaboration, and respectful interactions.

7. Experience chairing/leading review committees or other relevant regulatory governance committees.

8. Experience participating in cross-functional projects and teams.

9. Strong interpersonal skills and understanding of team dynamics.

10. Veeva PromoMats experience preferred.

11. When needed, ability to travel.

#LI-CS1, #LI-Remote

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