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Regulatory Program Manager Jobs in Alaska (NOW HIRING)

Program Manager

Anchorage, AK ยท On-site +1

$125K - $197K/yr

Specialized experience would include one year of substantive supervisory or program management ... Experience analyzing industry practices, regulatory provisions, and emerging trends to identify ...

ACT Program Manager

Bethel, AK ยท On-site

$83K - $108K/yr

ACT Program Manager Location: Bethel, Alaska Salary: $83,283 - $108,268/Year Employment Type ... and regulatory standards. Requirements * Master's Degree in Social Work, Counseling, Marriage ...

The program manager performs all clinical interventions and supervisory responsibilities in a ... Services are to be provided in compliance with licensure requirements, regulatory and practice ...

Program Manager - Long Term Care

Sitka, AK ยท On-site

$36.46 - $51.29/hr

Manages system for orientation and onboarding of employees. Participate in the development ... Conducts regulatory and policy review and updates in coordination with DON and Administrator.

Overview Regulatory Permitting Manager Pay Status : Full-Time Salary FLSA Status : Exempt Location ... Employee Assistance Program (EAP): Free counseling and support services * Paid Holidays: Observance ...

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Showing results 1-20

Regulatory Program Manager information

See Alaska salary details

$41.5K

$115.7K

$169.1K

How much do regulatory program manager jobs pay per year?

As of Aug 9, 2026, the average yearly pay for regulatory program manager in Alaska is $115,729.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,600.00 and $142,700.00 per year, depending on experience, location, and employer.

What are some common challenges faced by regulatory program managers, and how can they be addressed in day-to-day work?

Regulatory Program Managers often encounter challenges such as navigating evolving regulatory requirements, coordinating across multiple departments, and ensuring timely submissions to regulatory bodies. Staying updated on changes in regulations and fostering strong communication with cross-functional teams are key to overcoming these hurdles. Leveraging project management tools and establishing clear processes can also help maintain compliance and keep projects on track. Building relationships with regulatory agencies and internal stakeholders further facilitates smoother approvals and minimizes delays.

What is the difference between Regulatory Program Manager vs Regulatory Affairs Specialist?

AspectRegulatory Program ManagerRegulatory Affairs Specialist
Required CredentialsBachelor's degree, certifications like RAC often preferredBachelor's degree, certifications like RAC often preferred
Work EnvironmentOversees multiple projects, manages teams, strategic planningFocuses on specific regulatory submissions, documentation, compliance
Employer & Industry UsageUsed in healthcare, pharmaceuticals, medical devicesCommon in similar industries, often collaborates with managers
Search & Comparison IntentUnderstanding managerial roles, project scopeDetailing compliance tasks, submission processes

The Regulatory Program Manager typically oversees multiple regulatory projects, manages teams, and develops strategic compliance plans. In contrast, the Regulatory Affairs Specialist focuses on preparing documentation, ensuring regulatory compliance for specific products, and supporting submissions. Both roles require similar credentials and are vital in regulated industries like healthcare and pharmaceuticals, but they differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as a regulatory program manager?

To excel as a Regulatory Program Manager, you need expertise in regulatory compliance, project management, and industry-specific regulations, often supported by a relevant degree and certifications like PMP or RAC. Familiarity with regulatory submission systems, document management tools, and compliance tracking software is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing complex projects and diverse stakeholders. These abilities ensure regulatory objectives are met efficiently, reducing risks and supporting organizational success in a highly regulated environment.

What does a regulatory program manager do?

A Regulatory Program Manager oversees and coordinates regulatory compliance activities within an organization, often in industries such as pharmaceuticals, healthcare, finance, or energy. They ensure that the company meets all applicable laws, regulations, and industry standards by managing projects related to regulatory submissions, audits, and communications with regulatory agencies. Their role often includes developing strategies for regulatory approvals, monitoring changes in regulations, and working cross-functionally with other departments to maintain compliance. Effective Regulatory Program Managers help minimize compliance risks and support the organization's business objectives.
What job categories do people searching Regulatory Program Manager jobs in Alaska look for? The top searched job categories for Regulatory Program Manager jobs in Alaska are:
Infographic showing various Regulatory Program Manager job openings in Alaska as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $115,729 per year, or $55.6 per hour.

Program Manager, Regulatory Affairs

6AM City, LLC

False Pass, AK โ€ข On-site

$106 - $149/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New


Job description

Working Location: Minnesota, Brooklyn Park; Massachusetts, Westborough; Nationwide; Pennsylvania, Center Valley; Washington, Redmond

Workplace Flexibility: Hybrid

For more than 100 years, Olympus has focused on making people's lives healthier, safer and more fulfilling.

Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill their desires, dreams, and lives.

Our five Core Values empower us to achieve Our Purpose:

Patient Focus, Integrity, Innovation, Impact and Empathy.

Learn more about Life at Olympus: https://www.olympusamerica.com/careers.

Job Description

Assist the Manager, Regulatory Affairs in obtaining approval to market Olympus medical devices in the markets served by Olympus.

Job Duties
  • Facilitate development of regulatory strategy for novel technologies or market segments, that lead to product teams responsible for developing new products.
  • Where tasked by Regulatory Management, assist with Business Development opportunities, including due diligence assessments of regulatory posture, research, and capabilities.
  • Responsible for review and approval of product labeling (including IFU) and other ancillary labeling-related matters.
  • Work closely with Upstream Marketing and the Regulatory Labeling Team in developing labeling materials.
  • Responsible for development, coordination, preparation and maintenance of US medical device submissions such as Pre-Submissions, 510ks, PMAs, IDEs and applicable supplements and annual reports and liaise with FDA reviewers as needed.
  • Where designated, responsible for development, coordination, preparation and maintenance of medical device submissions for Canadian Class 2, 3 or 4 Device License submissions.
  • Lead development of responses to regulatory authorities' requests foradditional information.
  • Interface with International Regulatory Affairs Team to support preparation of dossiers for registration for other international markets such as Japan, the Far East, Australia and Latin America.
  • Responsible for keeping abreast of changes and proposed changes to the worldwide regulatory requirements related to our products and processes.
  • May be tasked to formally advise regulatory and business management of changes and as appropriate communicate regulatory initiatives orchanges to other OSTA staff.
  • Responsible for maintenance of regulatory files and tracking databases toensure prompt and accurate access to company regulatory information and to provide reports to management concerning current, pending, and future approvals to management.
Job QuaificationsRequired:
  • BS/BA required, preferably in engineering or life sciences. RAC accreditation or Post-graduate degree preferred.
  • Regulatory affairs experience in the Medical Device industry is mandatory (minimum 10 years with BS/BA, or 7 years with MS preferred).
  • Regulatory affairs experience in writing US submissions and EU submissions is mandatory.
  • Experience in collaboration and working with the Regulatory Authorities directly is mandatory.
Why join Olympus?Equitable Offerings you can count on:
  • Competitive salaries, annual bonus and 401(k)* with company match
  • Comprehensive medical, dental, vision coverage effective on start date
  • 24/7 Employee Assistance Program
  • Free live and on-demand Wellbeing Programs
  • Generous Paid Vacation and Sick Time
  • Paid Parental Leave and Adoption Assistance*
  • 12 Paid Holidays
  • On-Site Child Daycare, Cafรฉ, Fitness Center**

*US Only

Connected Culture you can embrace:
  • Work-life integrated culture that supports an employee centric mindset
  • Offers onsite, hybrid and field work environments
  • Paid volunteering and charitable donation/match programs
  • Employee Resource Groups
  • Dedicated Training Resources and Learning & Development Programs
  • Paid Educational Assistance
Center Valley, PA and Westborough, MA

The anticipated base pay range for this full-time position in this location is $106,402.00 - $148,963.00 / year, plus potential for annual bonus (subject to plan eligibility and other requirements).

Olympus considers a variety of factors when determining actual compensation for this position, including level of experience, working location, and relevant education and certifications.

At Olympus, we are committed to Our Purpose of making people's lives healthier, safer and more fulfilling. As a global medical technology company, we partner with healthcare professionals to provide best-in-class solutions and services for early detection, diagnosis

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