Companies nationwide are actively searching for a skilled regulatory specialist to help navigate complex compliance landscapes, and remote opportunities are growing fast. With 500+ open positions currently available, this is an excellent time to explore regulatory specialist jobs in the USA that offer flexibility without sacrificing career growth. Organizations across pharmaceuticals, healthcare, and manufacturing sectors are expanding their compliance teams to meet evolving regulations.
Successful candidates typically bring strong analytical skills, attention to detail, and a solid understanding of regulatory frameworks such as FDA, EMA, or ISO standards. Excellent written communication is essential, since the role often involves preparing submissions, reviewing documentation, and liaising with regulatory agencies. Employers seeking to hire a regulatory specialist also value proficiency in regulatory software systems, adaptability to changing guidelines, and the ability to manage multiple projects simultaneously while maintaining accuracy under tight deadlines.
Remote work has become the standard setup for many regulatory specialist positions, allowing professionals to collaborate with cross-functional teams through digital platforms while maintaining rigorous compliance standards. Companies across the USA increasingly favor distributed teams, recognizing that talent for this specialized field isn't confined to one region. This shift has fueled a steady rise in demand, making regulatory specialist vacancies more accessible to qualified professionals regardless of their physical location.
If you're ready to advance your career, now is the perfect moment to explore current regulatory specialist positions available through Global Work AI. Our platform connects talented professionals with employers seeking dedicated compliance experts ready to make an impact. Take the next step and discover how your expertise can fit into a thriving, remote-friendly industry today.
PacificSource
Monitor and report on Health Services operational activities and compliance with regulations. Conduct internal audits, oversee vendor compliance, and ensure adherence to clinical policies.
remote, GA, United States$71k – $106k/yrFull TimeSenior (5+ years)
CooperCompanies
Develop and execute regulatory strategies for medical devices and life science products. Prepare and maintain regulatory submissions, manage global product registrations, and ensure compliance with applicable regulations.
remote, Trumbull, CT, United States$80k – $107k/yrFull TimeJunior (<2 years)
Turing
Review and evaluate AI-generated responses to healthcare law hypotheticals, including HIPAA and FDA regulations. Apply a structured legal rubric to assess accuracy and compliance. Identify gaps in AI reasoning regarding fraud, abuse compliance, and clinical trial regulations.
remote, United States$202k – $403k/yrPart TimeMiddle (2-4 years)
Amerihealth Caritas
Lead the development and implementation of business and technical solutions for regulatory reporting. Identify and implement process enhancements for data integrity and efficiency. Coordinate with internal and external contacts to resolve reporting issues.
remote, Central, United StatesFull TimeLead / Manager
Vantage Risk Companies
Conduct regulatory reporting for insurance entities, ensuring timely submissions to state and federal agencies. Manage adjuster licensing, including renewals and compliance monitoring. Process producer license applications and maintain organized records.
remote, Chicago, IL, United States$120k – $140k/yrFull TimeSenior (5+ years)
Siemens Healthineers
Prepare and maintain regulatory submissions, including FDA 510(k) and IVDR Class C recertifications. Serve as a subject matter expert in Regulatory Affairs, guiding design control and product development teams.
remote, United States$127k – $174k/yrFull TimeSenior (5+ years)
Zimmer, Inc.
Assist with regulatory submissions, including authoring and publishing electronic submissions. Provide regulatory direction to development teams, evaluate risks of regulatory strategies, and review labeling for compliance.
remote, United StatesFull TimeSenior (5+ years)
BD
Coordinate and prepare premarket applications to the US FDA, including 510(k) submissions. Prepare technical files for CE marking of products and provide regulatory guidance throughout product development.
remote, NJ, United States$136k – $217k/yrFull TimeSenior (5+ years)
Environmental Research Group
Lead and support environmental compliance projects, conduct regulatory research, write reports, and assist in the permitting process. Perform site visits and surveys, ensuring compliance with federal and state regulations. Collaborate with team members while prioritizing client needs and deadlines.
remote, United States$80k – $90k/yrFull TimeJunior (<2 years)
Saratoga Medical Center
Prepare and review IND/IDE applications, protocol amendments, and annual reports. Manage regulatory correspondence and support FDA meetings, including pre-IND interactions.
remote, United StatesFull TimeSenior (5+ years)Lifelancer
Guide product and engineering teams on global regulatory planning and dossier compilation. Review and verify platform outputs, ensuring submission readiness and compliance with health authority data standards. Build a library of regulatory scenarios to enhance platform performance.
remote, MA, United States$120k – $180k/yrFull TimeSenior (5+ years)Saratoga Ascend
Prepare and review IND/IDE applications, protocol amendments, and safety reports. Support FDA meetings and manage regulatory correspondence. Maintain regulatory files and submission trackers while ensuring compliance with FDA regulations for investigator-sponsored studies.
remote, United StatesFull TimeSenior (5+ years)
Meridian Bioscience, Inc.
Support Regulatory Affairs, Design Quality Assurance, and software compliance for IVD instruments. Ensure compliance with design control, software lifecycle, and quality system requirements through documentation review and validation activities.
remote, United StatesFull TimeJunior (<2 years)
Topcon Positioning Systems
Support the development and improvement of the Quality Management System, ensuring compliance with FDA QMSR and ISO 13485. Manage risk for medical device software, including risk analysis and verification.
remote, United States$100k – $120k/yrFull TimeSenior (5+ years)
Evergen
Manage the promotional review process, coordinating the review and approval of advertising and promotional materials. Serve as the liaison for internal teams and external partners, ensuring submission readiness and compliance with regulatory standards.
remote, United StatesFull TimeMiddle (2-4 years)
Volga Partners
Evaluate AI-generated legal content for accuracy and compliance, assess legal reasoning and interpretations, verify information against authoritative sources, identify errors and inconsistencies, and provide structured feedback on findings.
remote, United States$36k – $91k/yrFull TimeMiddle (2-4 years)
Dawar Consulting, Inc.
Lead the preparation, publishing, validation, and electronic submission of regulatory dossiers for diagnostic products. Compile submission packages using tools like Veeva Vault and LORENZ docuBridge.
remote, NJ, United StatesFull TimeSenior (5+ years)
Getinge
Lead regulatory labeling strategy for SWICC consumable medical devices, managing a high volume of labels and versions. Monitor FDA and international labeling requirements, guiding cross-functional teams on compliance.
remote, United States$120k – $150k/yrFull TimeSenior (5+ years)
Lennar
Monitor federal, state, and agency regulations to provide compliance guidance. Assist in developing and implementing policies and procedures, conducting compliance monitoring, and preparing for audits and regulatory examinations. Review marketing and advertising for compliance with TILA regulations.
remote, Tallahassee, FL, United StatesFull TimeMiddle (2-4 years)
Ruger Firearms
Serve as the liaison between Corporate Compliance and Manufacturing Compliance Coordinators. Coordinate ATF compliance initiatives and monitor facility compliance activities. Administer ATF licensing, recordkeeping, and NFA compliance activities.
remote, United StatesFull TimeJunior (<2 years)
JMS Technical Solutions
Review and propose revisions to claim substantiations based on scientific evidence. Collaborate with Regulatory, Research, Product Development, and Marketing teams to ensure compliance with regulations.
remote, United States$105k – $120k/yrFull TimeMiddle (2-4 years)
IMMY
Prepare and maintain U.S. FDA regulatory submissions for in vitro diagnostic products, including 510(k), PMA, and De Novo submissions. Manage Q-Submissions and FDA interactions, ensuring compliance with regulatory requirements.
remote, United StatesFull TimeMiddle (2-4 years)Moffitt Cancer Center
Support research activities by completing protocol-specific documents and standardized reports. Ensure compliance with internal policies, IRBs, and federal regulations. Draft informed consent documents, process BioSafety applications, and submit application documents to the respective IRB.
remote, United States$48k – $73k/yrFull TimeMiddle (2-4 years)
Singota Solutions
Assist in regulatory affairs and compliance programs, providing regulatory guidance to clients. Manage regulatory documentation, support licensing and certification processes, and conduct regulatory surveillance.
remote, IN, United StatesFull TimeMiddle (2-4 years)
SAIC
Provide regulatory support for Food Facility Registration and Complaint Programs, including adverse event reporting and product problem tracking. Manage program records, coordinate cross-functional activities, and ensure timely processing of regulatory submissions.
remote, United StatesFull TimeMiddle (2-4 years)
Recover Medical Group
Support regulatory compliance, audit readiness, licensing, and quality improvement efforts. Coordinate timely submissions for audits and external quality reviews, manage state and county reporting requirements, and monitor EHR reports for data accuracy.
remote, CA, United StatesFull TimeJunior (<2 years)STEM Search Group
Guide product teams through the regulatory submission process for software development, identifying evidence gaps. Prepare U.S. and international submission packages for new and modified medical devices. Evaluate updates to software, firmware, and hardware for filing requirements.
remote, NY, United States$125k – $140k/yrFull TimeSenior (5+ years)
Agile Space Industries, Inc.
Support export-control and trade compliance activities, including ITAR and EAR requirements. Lead export jurisdiction assessments and assist with licensing and authorization requirements. Develop and improve compliance policies and procedures, and maintain accurate compliance records.
remote, North Carolina, United States$104k – $130k/yrFull TimeSenior (5+ years)
Function Health
Partner with product managers to set regulatory paths for new features, review claims and user experiences, prepare regulatory launch documentation, and author FDA submissions.
remote, United StatesFull TimeSenior (5+ years)
Zoetis
Lead global surveillance workstreams, monitor and communicate regulatory requirements, coordinate cross-functional impact assessments, and manage regulatory intelligence communications.
remote, United States$120k – $180k/yrFull TimeLead / Manager
Mohawk Global Logistics Corp
Manage post-entry processes, product classifications, and regulatory documentation to ensure compliance with U.S. Customs and Participating Government Agency requirements. Prepare post-entry filings, maintain compliance documentation, and support internal teams with compliance-related requests.
remote, Atlanta, GA, United StatesFull TimeJunior (<2 years)
Medexus Pharma Careers
Manage Chemistry, Manufacturing and Controls (CMC) change controls and regulatory assessments for pharmaceutical products in Canada and the U.S. Prepare post-approval submissions, coordinate documentation with internal teams and external partners, and ensure compliance with regulatory requirements.
remote, United States$74k – $104k/yrFull TimeSenior (5+ years)
Evergen
Lead regulatory support for product development teams, including preparing regulatory documents and coordinating labeling activities. Review and approve design control documentation and risk management reports. Maintain awareness of global regulatory changes and assess their impact.
remote, United States$100k – $115k/yrFull TimeSenior (5+ years)Moffitt Cancer Center
Evaluate and complete protocol-specific documents and reports for compliance in research activities. Process IRB applications, maintain informed consent forms, and assist with audit documentation.
remote, United States$60k – $92k/yrFull TimeLead / Manager
SOLVENTUM
Lead a regulatory affairs team supporting Restorative Healing Technologies. Develop and execute regulatory strategies for product market authorizations, manage cross-functional stakeholder decisions, and participate in strategic meetings.
remote, United States$124k – $171k/yrFull TimeSenior (5+ years)
Dane Street, LLC
Lead the application, acquisition, and renewal of state licenses and regulatory registrations, including URO and IRO filings. Monitor state laws and regulations to ensure compliance, respond to compliance requests and audits, and maintain compliance documentation.
remote, United StatesFull TimeJunior (<2 years)Zimmer, Inc.
Assist with assembly, distribution, and tracking of regulatory information; author electronic submissions; respond to foreign government requests for marketing approval documentation; provide regulatory direction to project teams; evaluate risks of regulatory strategies; review labeling and…
remote, United States$109k/yrFull TimeSenior (5+ years)C2 Environmental Inc
Assist with transmission line rebuild and routing applications, including permit applications and environmental documentation. Conduct research, prepare reports, perform data compilation and quality control, and complete GIS mapping and analysis.
remote, United StatesFull TimeJunior (<2 years)
RYZE
Review product labels and packaging for FDA compliance, evaluate claims substantiation, and coordinate regulatory clearance for new product launches.
remote, United StatesFull TimeMiddle (2-4 years)
Parsons Corporation
Maintain a tracking matrix of permits, approvals, and regulatory compliance milestones. Verify the status of regulatory approvals and flag compliance gaps. Track requirements from local building departments and state environmental agencies.
remote, United States$88k – $155k/yrFull TimeSenior (5+ years)10,000,000+ more jobs available!
