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Regulatory Program Manager Jobs in Massachusetts

Diamond Antenna and Microwave

PROGRAM MANAGER

Brockton, MA · On-site

$120K - $140K/yr

Ensure compliance with contractual requirements, industry standards, and regulatory requirements ... Experience with program management tools such as Microsoft Project, Jira, Smartsheet, or Primavera.

DIAMOND ANTENNA & MICROWAVE

PROGRAM MANAGER

Brockton, MA · Hybrid

$120K - $140K/yr

Ensure compliance with contractual requirements, industry standards, and regulatory requirements ... Experience with program management tools such as Microsoft Project, Jira, Smartsheet, or Primavera.

Applied Research Solutions

Program Manager

Bedford, MA · On-site

$130K - $152K/yr

Provide Program Management inputs to Request for Proposal (RFPs) including systems specs ... Support, prepare, review and develop acquisition reports, including statutory and regulatory ...

Clinovo

Program Manager

Cambridge, MA · On-site

Coordinate activities across Clinical Development, Regulatory Affairs, Nonclinical Development ... Experience managing multiple development programs simultaneously is preferred.

HX5 LLC

Program Manager

Bedford, MA · On-site

$130K - $154K/yr

Program Manager Program Manager, Senior Hanscom Air Force Base HX5 is an award-winning provider of ... Must be able to support and develop acquisition reports, including statutory and regulatory reports ...

CPI International

Program Manager

Hudson, MA · On-site

$110K - $140K/yr

Ensure compliance with safety standards, regulatory requirements (e.g., FAA, DoD), and internal ... Experience managing programs for both defense and commercial aerospace sectors, with a focus on ...

Busek Co Inc

Program Manager

Natick, MA · On-site

$110K - $180K/yr

Summary: As a Program Manager, you will oversee the planning, development, and execution of ... Government space technology export regulations, including the International Traffic in Arms ...

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All JobsRegulatory Program JobsRegulatory Program Manager JobsRegulatory Program Manager Jobs in Massachusetts

Regulatory Program Manager information

See Massachusetts salary details

$42K

$117.4K

$171.5K

How much do regulatory program manager jobs pay per year?

As of Aug 23, 2026, the average yearly pay for regulatory program manager in Massachusetts is $117,360.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,800.00 and $144,700.00 per year, depending on experience, location, and employer.

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 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 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 popular job titles related to Regulatory Program Manager jobs in Massachusetts?

For Regulatory Program Manager jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Regulatory Program Manager jobs in Massachusetts look for?

The top searched job categories for Regulatory Program Manager jobs in Massachusetts are:

What cities in Massachusetts are hiring for Regulatory Program Manager jobs?

Cities in Massachusetts with the most Regulatory Program Manager job openings:

Regulatory Program Manager jobs near you
Infographic showing various Regulatory Program Manager job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $117,360 per year, or $56.4 per hour.

Regulatory Affairs Program Manager

Stark Pharma Solutions Inc

Raynham, MA • On-site

Contractor

Re-posted 17 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Regulatory Affairs Program Manager position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Job Title: Regulatory Affairs Program Manager (Medical Device – Divestiture)

Location: Raynham, MA / West Chester, PA / Palm Beach Gardens, FL (Hybrid – 3–4 days onsite)
Duration: 12+ Months (Extension Possible)
 

We are seeking an experienced Regulatory Affairs Program Manager to lead a large-scale Medical Device Divestiture initiative. This role will manage the transfer of global regulatory registrations, submissions, and documentation from a large healthcare organization to a newly established medical device company while ensuring regulatory compliance and seamless execution.

Key Responsibilities:

  • Lead regulatory activities supporting a global divestiture program.
  • Complete and execute the Regulatory Registration Transfer Strategy.
  • Manage ownership transfers, amendments, renewals, notifications, and new submissions.
  • Coordinate with cross-functional Regulatory, Quality, and Project teams.
  • Identify project risks, develop mitigation plans, and ensure GMP compliance.
  • Maintain project documentation, timelines, and stakeholder communication.

Required Skills:

  • 10+ years of Regulatory Affairs experience in the Medical Device industry.
  • Hands-on experience with Divestiture/Business Separation projects.
  • Strong Regulatory Program Management experience.
  • Expertise with FDA 510(k), PMA, global registrations, labeling changes, design changes, and regulatory submissions.
  • Knowledge of registration ownership transfers, submission pathways, and health authority interactions.
  • Excellent communication, leadership, and stakeholder management skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com