Regulatory Affairs Specialist Jobs in Pennsylvania
Regulatory Affairs Specialist jobs in Pennsylvania are open across King of Prussia, Exton, and West Chester and other Pennsylvania metros, with employers like Globus Medical, Katalyst Healthcares & Life Sciences, and West Pharmaceutical Services hiring at every experience level. Find a role that fits below and apply directly.
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At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible.
Position Summary
Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements. Compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and improves tracking and control systems. Keeps abreast of regulatory procedures and changes. Recommends strategies for earliest possible approvals of clinical trials applications.
Essential Functions
- Determines the appropriate regulatory strategy for new products and documents all related activities to remain in compliance
- Demonstrates global regulatory expertise in product submissions and evaluates changes with local regulations
- Collaborates with various departments to review the required plans, procedures and regulatory decisions for new or existing products
- Reviews regulatory requirements from other departments for new product designs or changes to existing designs
- Reviews technical publications, articles, and abstracts to stay abreast of regulatory and technical developments in the industry
- Prepares and maintains regulatory pre-market submissions and other pre-market filings to assist in acquiring appropriate commercial distribution clearances
- Supports product import by providing applicable regulatory documentation and certificates
- Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies
- Ensures compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role
- Represents the company in a professional manner and upholds the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Qualifications
- Typically requires a minimum of 5 years of related experience with a Bachelor’s degree; or 3 years and a Master’s degree; or a PhD without experience; or equivalent work experience
- 5+ years of related experience in the medical device industry
- Understanding of regulatory requirements throughout the product lifecycle
- Solid understanding of regulatory terminology, pre-market submission types, and requirements
- Able to evaluate regulatory impact of proposed product and process changes
- Capable multi-tasking skills with the ability to project plan and meet deadlines
- Result driven with a sense of responsibility, urgency and ability to perform under pressure
Physical Demands
The physical demands listed here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
- Required to sit; climb or balance; and stoop, kneel, crouch or crawl
- Required to regularly lift and/or move up to 10 pounds, and occasionally lift and/or move up to 25 pounds
- Required to possess specific vision abilities, including close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus
Our Values
Our Life Moves Us philosophy is built on four values: Passionate About Innovation, Customer Focused, Teamwork, and Driven.
- Passionate about Innovation: Improving patient care by delivering advanced technology to our customers is at the core of what we do. We are passionate in our role in improving the lives of patients by continuously developing better solutions.
- Customer Focused: We listen to our customers’ needs and respond with a sense of urgency.
- Teamwork: Working together, anything is possible. We value every person on our team and treat each other with respect. We are accountable to one another and support each other. Together, we make each other stronger.
- Driven: We pursue our mission with energy and passion. We are nimble, results-oriented and decisive. We overcome obstacles that arise in our quest to deliver solutions that will improve the lives of our customers and patients.
Equal Employment Opportunity
Globus Medical is an equal opportunity employer. All applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, age, disability, marital status, pregnancy, national origin or citizenship. We are committed to a diverse workforce. We value all employees’ talents and support an environment that is inclusive and respectful.
Other Duties
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.
See All 5 Regulatory Affairs Specialist Jobs in Pennsylvania
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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
- Globus Medical3

- Katalyst Healthcares & Life Sciences1

- West Pharmaceutical Services1

Top Industries Hiring
- Healthcare & Medical Services3
- Medical Devices3
- Chemicals & Materials1
- Consulting & Professional Services1
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, engineering, or a related field
- Experience preparing and submitting regulatory filings such as 510(k), PMA, NDA, or BLA
- Knowledge of FDA regulations including 21 CFR parts relevant to the product type
- Proficiency with regulatory information management systems such as Veeva Vault or RIMS
- Regulatory Affairs Certification (RAC) from RAPS preferred for senior roles
- Strong technical writing skills for preparing regulatory summaries, briefing documents, and SOPs
Regulatory Affairs Specialist Jobs in Pennsylvania: Frequently Asked Questions
How many regulatory affairs specialist jobs are there in Pennsylvania?
There are 5+ regulatory affairs specialist openings in Pennsylvania on Migrate Mate as of June 2026, with the most roles in King of Prussia, Exton, and West Chester. New positions post regularly as employers across Pennsylvania hire.
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 Pennsylvania cities have the most regulatory affairs specialist jobs?
King of Prussia, Exton, and West Chester have the most regulatory affairs specialist openings in Pennsylvania right now, with additional roles spread across smaller metros statewide.
Which companies hire regulatory affairs specialists in Pennsylvania?
Employers hiring regulatory affairs specialists in Pennsylvania include Globus Medical, Katalyst Healthcares & Life Sciences, and West Pharmaceutical Services, based on current listings on Migrate Mate as of June 2026.
Are there remote regulatory affairs specialist jobs in Pennsylvania?
Yes. About 20% of regulatory affairs specialist openings tied to Pennsylvania are remote or hybrid as of June 2026. The rest are on-site roles based in Pennsylvania metros.
How do I apply for regulatory affairs specialist jobs in Pennsylvania?
You can apply to regulatory affairs specialist jobs in Pennsylvania directly on Migrate Mate. Search the listings above, find roles that match your experience and preferred Pennsylvania location, then apply to each one that fits.
See All 5 Regulatory Affairs Specialist Jobs in Pennsylvania
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