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Program Manager, Regulatory Affairs

Olympus Corporation of the Americas

Center Valley, PA · HybridFull-time$106–149K/yrSeen todaySeen in employer's feed today

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At a glance

Compensation
$106–149K/yr
Location
Center Valley, PAHybrid
Schedule
Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Program Manager, Regulatory Affairs assists with obtaining market approval for Olympus medical devices. The role develops regulatory strategies and submissions, reviews product labeling, coordinates responses to regulatory authorities, and supports registrations in international markets. It is a hybrid position based in Center Valley, Pennsylvania, or Westborough, Massachusetts. The posting requires substantial medical-device regulatory affairs experience, including writing US and EU submissions and working directly with regulatory authorities.

Skills & qualifications

RequiredNice to have

Skills

Regulatory Strategy DevelopmentRegulatory Due DiligenceProduct Labeling ReviewUS Medical Device SubmissionsEU Medical Device SubmissionsRegulatory Authority Collaboration

Qualifications

Bachelor's Degree10+ Years Regulatory Affairs Experience With Bachelor's7+ Years Regulatory Affairs Experience With Master'sRAC AccreditationPostgraduate Degree

Benefits

401(k) Match
Medical Insurance
Dental Insurance
Vision Insurance
Paid Time Off
Parental Leave
Tuition Assistance

Full job description

Working Location: Massachusetts, Westborough; Pennsylvania, Center Valley

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 themarkets 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 Qualifications

Required:

  • 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?

We offer a holistic employee experience supporting personal and professional well-being through meaningful work, equitable offerings, and a connected culture.

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, Café, Fitness Center**

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

*US Only

**Center Valley, PA and Westborough, MA

Are you ready to be a part of our team?

Learn more about our benefits and incentives: https://www.olympusamerica.com/careers/benefits-perks .

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 and minimally invasive treatment, aiming to improve patient outcomes by elevating the standard of care in targeted disease states.

For more than 100 years, Olympus has pursued a goal of contributing to society by producing products designed with the purpose of delivering optimal outcomes for its customers around the world.

Headquartered in Tokyo, Japan, Olympus employs more than 31,000 employees worldwide in nearly 40 countries and regions. Olympus Corporation of the Americas, a wholly owned subsidiary of Olympus Corporation, is headquartered in Center Valley, Pennsylvania, USA, and employs more than 5,200 employees throughout locations in North and South America. For more information, visit www.olympusamerica.com .

You Belong at Olympus

We are deeply committed to fostering a respectful, fair, and welcoming workplace for all individuals, perspectives, and lifestyles. We believe in fostering a non-discriminatory, inclusive work environment where everyone feels a sense of belonging, in full compliance with legal standards. Empathy and unity are core to our company culture, empowering employees to contribute fully and flourish. We warmly encourage all who wish to bring their talents to Olympus to apply.

Applicants Requesting Accommodations: Olympus is committed to the full inclusion of all qualified individuals. As part of this commitment, Olympus will ensure that persons with disabilities are provided reasonable accommodations for the hiring process. If reasonable accommodation is needed, please contact [email protected]. If your disability impairs your ability to email, you may call our HR Compliance Manager at 1-888-Olympus (1-888-659-6787).

Let’s realize your potential, together.

It is the policy of Olympus to extend equal employment and advancement opportunity to all applicants and employees without regard to race, color, national origin (including language use restrictions), citizenship status, religious creed (including dress and grooming practices), age, sex (including pregnancy, childbirth, breastfeeding, medical conditions related to pregnancy, childbirth and/or breastfeeding), gender, gender identity and expression, sexual orientation, marital status, disability (physical or mental) and/or a medical condition, genetic information, ancestry, veteran status or service in the uniformed services, and any other characteristic protected by applicable federal, state or local law.

Posting Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs (QA/RA)

How this job compares

Set against the 996 open Regulatory Affairs jobs on Olive Jobs, counted November 4, 2026.

Pay
  • This posting$106–149K/yr
  • Pennsylvania median$126–201K/yr25 salary ranges
  • US median$142–201K/yr658 salary ranges

This range's midpoint, $128K, is 20% below the Pennsylvania median midpoint ($159K) — in the lowest quarter of Regulatory Affairs salary ranges in Pennsylvania.

Openings
Olive Jobs lists 52 open Regulatory Affairs jobs in Pennsylvania and 996 across the US. 15% of them nationwide are listed as remote or flexible.
Hiring the most in Pennsylvania
Experience
This posting asks for at least 10 years of experience; Regulatory Affairs postings that state a minimum ask for 7 years at the median (864 postings).
Education
This posting asks for a bachelor's degree; 621 of the 996 open Regulatory Affairs jobs (62%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 4, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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