Regulatory Writing Jobs

Lead and execute complex EHS compliance programs and audits for clients as a Senior Safety, Health & Environment Specialist on AECOM’s Environmental Health & Safety team.

Experienced regulatory technical writer needed to author and manage CMC submission content for cell therapy programs in a hybrid, cross-functional PMO environment.

AECOM seeks an experienced Air Quality Engineer in Chelmsford, MA to lead air permitting, regulatory compliance, and emissions inventory work while supporting client-facing projects and proposals.

An Associate Medical Writer role at a global medical communications agency supporting preparation of scientific materials (abstracts, posters, manuscripts, slide decks) and collaborating with cross-functional teams on client deliverables.

Staff Scientist at the University of Rochester's Del Monte Institute to lead complex research projects, supervise lab personnel, and contribute to publications and program development.

AECOM is hiring a Senior Environmental Planner/Permitting Specialist in Piscataway, NJ to lead NEPA documentation and regulatory permitting for major transportation infrastructure projects.

FINRA’s Office of Strategic Engagement is hiring a Senior Principal Analyst to lead high-impact publications, speaker materials, and external messaging that advance regulatory oversight and industry engagement.

AECOM seeks an experienced Environmental Remediation Project Manager in Dallas to lead remediation projects, manage client relationships, and deliver projects on scope, schedule, and budget.

DELC is hiring a bilingual (English/Spanish) Licensing Specialist to conduct licensing visits, compliance reviews, and investigations that protect children and support early learning providers across the region.

Lead cross-functional clinical readiness efforts for complex devices and combination products within AbbVie's DCPD organization to enable early-stage clinical trials.

Lead Aidoc's clinical research strategy and team to deliver rigorous studies and publications that validate AI-driven medical solutions and support market adoption.

Lumafield is hiring a Regulatory Affairs Specialist to define and execute regulatory strategy and compliance processes for its industrial CT hardware-software products.

Lead Aidoc's clinical research strategy and team to deliver rigorous studies and publications that validate AI-driven medical solutions and accelerate clinical adoption across the U.S.

ProSidian is hiring a seasoned Technical Editor to produce and manage high-quality, controlled technical documentation supporting DOE-EM Hanford tank waste and treatment program activities.

M&T Bank seeks an experienced Credit Policy Manager to rebuild, govern and maintain the bank’s Credit Policy Manual across NY locations in a hybrid role.

Commonwealth Fusion Systems is hiring a Public Policy Intern in Devens, MA to support research, policy drafting, and stakeholder engagement to advance commercial fusion energy deployment.

Serve as an Associate Project Manager within AbbVie's DCPD team to coordinate device and drug delivery system readiness for early-stage clinical trials across cross-functional partners.

Lead clinical evidence strategy for neuromodulation and pelvic health by developing integrated evidence roadmaps and applying RWE and AI to accelerate therapy adoption and access.

QRC Group is hiring a Specialist QA in Juncos, Puerto Rico to lead validation, commissioning/qualifications and quality system activities for manufacturing operations.

Experienced regulatory scientist (M.S. or Ph.D.) needed to lead pesticide registration strategy and client-facing regulatory work within Exponent’s Chemical Regulation and Food Safety Practice in Washington, DC.

Experienced environmental or engineering professional needed to lead compliance reviews and conduct statewide site inspections for energy facility siting at the Oregon Department of Energy in a hybrid-remote role.

Legal Researcher (Mandarin/English) — a remote role at Jerry.ai supporting the General Counsel with bilingual legal research, contract drafting and compliance across U.S. and China-related product and regulatory matters.

OLCC is hiring Recreational Marijuana Inspectors to perform field and office-based compliance investigations, inventory audits, and enforcement activities for Oregon's recreational cannabis industry.

Lead the clinical research strategy for an AI-driven medical imaging company, overseeing studies, publications, and a growing team in a remote US role.

Lead Western Digital’s sustainability reporting, policy development, and ESG ratings engagement to strengthen disclosures and regulatory readiness.

Foresight Diagnostics seeks a Senior Specialist, Regulatory Affairs to lead US regulatory strategy and submissions for next-generation sequencing-based IVD products while partnering cross-functionally through development and lifecycle management.

The NYC Health Department seeks a Public Health Sanitarian to perform inspections of child care programs citywide, enforce regulations, document findings, and support child health and safety initiatives.

Serve as the Compliance Officer at the NYC Mayor's Office of Minority and Women-owned Business Enterprises to lead regulatory research, policy drafting, audits, and stakeholder training that ensure compliance with Administrative Code 6-129.

Lead Aidoc's clinical research efforts to design, execute, and publish high-quality studies that validate AI-enabled medical solutions and accelerate market adoption across the U.S.

Gilead is hiring a Sr. Human Factors Engineer I to drive HFE strategy and usability testing for combination product development at our Foster City site.

USAA is hiring an Advocacy Advisor-Intermediate in San Antonio to manage escalated member complaints, perform root-cause research, and deliver compliant resolutions across verbal and written channels.

USAA is hiring an Advocacy Advisor-Intermediate in San Antonio to investigate and resolve escalated banking and regulatory complaints with accurate documentation, clear communication, and risk-aware solutions.

Klick Health seeks an experienced Medical Writer on a 3-month contract to develop clear, strategic scientific content across medical communications deliverables while working closely with cross-functional teams and clients.

ActiGraph is hiring a Senior Compliance Specialist to lead QMS and regulatory compliance activities across product development, post-market surveillance, and audits for their medical-grade wearable solutions.

Lead strategic regulatory labeling activities for AbbVie’s US/EU products, coordinating cross-functional teams to ensure compliant, consistent and optimized product labeling.

Allucent seeks a seasoned VP, CMC (contractor) to lead regulatory strategy, CMC development, and global Health Authority interactions to accelerate life-changing therapies.

Serve as an experienced regulatory leader providing CMC strategy, hands-on submission support, and Health Authority engagement to advance drug, biologic, and device programs for Allucent clients.

AbbVie is hiring a Senior Clinical Pharmacologist (Immunology) to lead PK/PD strategy, modeling and regulatory pharmacology contributions for immunology programs at its North Chicago site.

CNO Financial Group seeks a motivated JD student (completed 1L) for a paid Summer 2026 Legal Internship to perform legal research, draft documents, and support cross-functional legal matters in a regulated insurance environment.

Experienced clinical pharmacology leader needed to shape PK/PD strategy, lead cross-functional projects, and represent AbbVie in regulatory and business development settings at the North Chicago site.

Lead device and combination product regulatory strategy and submissions at AbbVie to support timely approvals and market access.

Blink Health is hiring a Regulatory Counsel to provide legal and policy guidance on federal and state healthcare and pharmaceutical regulatory matters while supporting advocacy and cross-functional compliance efforts.

AbbVie seeks specialist physicians (MD/DO) for a two-year Physician Development Program based in North Chicago to develop clinical research and medical affairs expertise through rotational assignments across R&D functions.

AbbVie seeks early-career physician specialists to participate in a two-year onsite Physician Development Program in North Chicago, rotating through core R&D functions as Associate Medical Directors.

AbbVie’s two-year Physician Development Program prepares graduating fellows for careers in R&D by providing onsite rotations and mentorship across clinical development, safety, medical affairs and regulatory functions.

Lead and grow an environmental planning practice in San Jose by driving business development, directing CEQA/NEPA projects, and mentoring a multidisciplinary team.

Senior medical writer and team lead role responsible for authoring regulatory submissions and maturing medical writing processes at a growth-stage biotech focused on immunology.

Serve as the primary regulatory investigator for Muckleshoot Tribal gaming operations, enforcing gaming integrity and responding to incidents under Tribal, state, and federal authorities.

AbbVie is hiring a Scientific Director in Medical Affairs (Oncology) to lead medical strategy, evidence generation, and safety oversight for oncology/hematology programs based in Mettawa, IL (hybrid; remote candidates considered).

AbbVie is hiring a Senior Project Engineer to lead and deliver complex engineering projects for drug product manufacturing and packaging at its Cincinnati site.