Regulatory Affairs Specialist Jobs in Pennsylvania
Regulatory Affairs Specialist jobs in Pennsylvania are among the most active in the country, concentrated in pharmaceuticals, medical devices, and life sciences, with openings at every level from entry-level associate to senior principal. The heaviest hiring clusters around Philadelphia, Pittsburgh, and the Route 202 corridor in the southeastern suburbs, where established employers like GSK, Merck, and Johnson and Johnson maintain significant operations. Drug approval submissions, quality systems compliance, and FDA regulatory strategy are the most in-demand specialties across Pennsylvania listings. Find a role that fits below and apply directly.
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Description
Penn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine. Working for this leading academic medical center means collaboration with top clinical, technical and business professionals across all disciplines.Today at Penn Medicine, someone will make a breakthrough. Someone will heal a heart, deliver hopeful news, and give comfort and reassurance. Our employees shape our future each day. Are you living your life's work?
- Entity: Corporate
- Department: Government Relations
- Location: Remote
- Hours: 8hr days
Summary:
The Senior Director, State Government Relations and Regulatory Affairs, in Penn Medicine's Department of Government and Community Relations is the health system's lead strategist and representative for all state-level legislative and regulatory matters. This role shapes and advances the organization's policy agenda with the Governor's Office, state agencies, the legislature, and key external partners. The Senior Director provides high-level counsel to executive leaders, anticipates emerging policy trends, and positions the health system as a key voice in state health policy, financing, and public health strategy. Reporting to the AVP of Government & Community Relations, the Director manages the Associate Director of Government Relations and coordinates state advocacy across all entities, departments, faculty and staff to facilitate communication with elected and appointed government officials. This position requires a moderate amount of travel (e.g. Harrisburg, PA and Trenton, NJ.)
Responsibilities:
- Leads the execution of the health system’s state advocacy agenda in both Pennsylvania and New Jersey. Oversee the development and implementation of Penn Medicine’s advocacy agenda. Establishes new relationships and strengthens existing relationships with state government officials and key staff in Harrisburg, PA and Trenton, NJ and their respective district offices.
- Responsible for coordinating regulatory stakeholders and experts on regulatory responses as it relates to government agencies.
- Communicates with internal and external constituencies by drafting reports and updates as necessary, including reports for the Penn Medicine Board of Trustees. This role will lead and manage the Government Relations weekly newsletter process, as well as internal and external updates from the department. Will draft advocacy correspondence on behalf of senior leadership outlining Penn Medicine’s position on current policy matters, and will brief senior leadership as necessary. Responsible for executive level coordination of state government relations with entity CEOs.
- Participates in meetings for industry associations and outside organizations focused on state government relations and health care policy, including but not limited to the Hospital & Healthsystem Association of Pennsylvania, the New Jersey Hospital Association and various chambers of commerce.
- Leads strategic initiatives and short- and long-term planning activities in collaboration with AVP and VP, including special projects and is the lead on projects as assigned.
- Direct and manage the Associate Director of Government and Community Relations to ensure alignment and coordination across entities.
- Leads and provides direction to a team of public affairs consultants who support the development and execution of Penn Medicine’s state advocacy agenda.
- Ensures compliance with lobbying disclosure and reporting requirements as applicable. Maintains ethical standards of conduct at all times.
Education or Equivalent Experience:
- Bachelor of Arts or Science Political Science/Public Administration or related fields (Required)
- 10+ years Extensive experience in the public sector and/or government relations positions. Knowledge of the legislative process, health care industry and health policy required. Position requires extensive knowledge of hospital issues such as Medicare and Medicaid reimbursement, hospital financing, and regulatory issues. (Required)
Live Your Life's Work
We are an Equal Opportunity employer. Candidates are considered for employment without regard to race, ethnicity, color, sex, sexual orientation, gender identity, religion, national origin, ancestry, age, disability, marital status, familial status, genetic information, domestic or sexual violence victim status, citizenship status, military status, status as a protected veteran or any other status protected by applicable law.
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Find JobsRegulatory Affairs Specialist Jobs by City in Pennsylvania
Where Pennsylvania roles are concentrated, by current openings.
Regulatory Affairs Specialist Job Market in Pennsylvania
A snapshot from current Pennsylvania openings, updated as new roles post.
Who's Hiring



Top Industries Hiring
- Medical Devices
- Chemicals & Materials
- Healthcare & Medical Services
- Consulting & Professional Services
What Pennsylvania Employers Look For
The qualifications that appear most often in regulatory affairs specialist jobs across Pennsylvania.
- Bachelor's degree in life sciences, chemistry, pharmacy, or a closely related field required
- Demonstrated experience with FDA submissions including INDs, NDAs, 510(k)s, or PMAs
- Working knowledge of 21 CFR regulations governing pharmaceuticals or medical devices
- Proficiency with regulatory document management systems such as Veeva Vault or ECTD tools
- Strong technical writing skills for regulatory documents, gap analyses, and SOPs
- RAC certification from the Regulatory Affairs Professionals Society preferred for senior roles
Regulatory Affairs Specialist Jobs in Pennsylvania: Frequently Asked Questions
How do you become a regulatory affairs specialist in Pennsylvania?
A bachelor's degree in a life science, pharmacy, chemistry, or engineering is the standard starting point for regulatory affairs specialists in Pennsylvania. No Pennsylvania state license is required for the role, but many employers expect or prefer the Regulatory Affairs Certification (RAC) credential issued by the Regulatory Affairs Professionals Society. Pennsylvania's dense pharmaceutical corridor means hiring managers often expect familiarity with FDA drug or device submission processes, so coursework or experience in those frameworks strengthens a candidacy significantly.
How much do regulatory affairs specialists make in Pennsylvania?
Regulatory affairs specialists in Pennsylvania earn a median of about $85,580 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $49,910 for the lowest 10% to over $130,990 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire regulatory affairs specialists in Pennsylvania?
Employers hiring regulatory affairs specialists in Pennsylvania right now include West Pharmaceutical Services, Globus Medical, and GSK, based on current listings on Migrate Mate as of September 2026. Pennsylvania's concentration of major pharmaceutical headquarters and regional medical device manufacturers means the pipeline of open positions tends to stay consistent across both large corporate teams and smaller specialty companies.
Which Pennsylvania cities have the most regulatory affairs specialist jobs?
Exton, Philadelphia, and Pittsburgh have the most regulatory affairs specialist openings in Pennsylvania. Philadelphia and its southeastern suburban corridor drive the largest share of listings because of the dense cluster of pharmaceutical and biotech headquarters there, while Pittsburgh contributes through its growing life sciences and hospital-affiliated research sector.
Are there remote regulatory affairs specialist jobs in Pennsylvania?
Yes, and more than most fields, because regulatory affairs work is primarily document-based and does not require hands-on lab or manufacturing presence. About 75% of regulatory affairs specialist openings tied to Pennsylvania are remote or hybrid as of September 2026, reflecting how well the role translates to distributed teams. Submission writing, gap analysis, and regulatory strategy functions are the most likely to be offered remotely.
How can I get hired as a regulatory affairs specialist in Pennsylvania with little or no experience?
The most realistic entry path is a regulatory affairs associate or coordinator role at a pharmaceutical or medical device company in the Philadelphia area, where many employers hire candidates with a relevant science degree and limited industry experience. GSK, Merck, and regional contract research organizations in Pennsylvania regularly post associate-level openings suited to recent graduates. Moving laterally from quality assurance, clinical data management, or scientific writing positions is common because those roles build directly transferable skills. Earning the RAC credential or completing a regulatory affairs certificate program gives candidates a clear edge over peers with comparable experience.
Where can I find and apply to regulatory affairs specialist jobs in Pennsylvania?
You can find and apply to regulatory affairs specialist jobs in Pennsylvania on Migrate Mate, which lists current Pennsylvania openings. Find roles that fit your background and apply directly to the ones that match.
See All 20 Regulatory Affairs Specialist Jobs in Pennsylvania
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