Regulatory affairs jobs in Union City, NJ - Page 2Create job alerts

Job DescriptionCompany Description We’re the world’s leading sports technology company, at the intersection between sports, media, and betting. More than 1,700 sports federations, media outlets, betting operators, and consumer platforms across 120 countries rely on our know-how and technology t...

Job Description Company Overview: With an annual budget of $2.3 billion and more than 7,000 employees throughout the five boroughs, the New York City Department of Health and Mental Hygiene (NYC DOHMH) is one of the largest public health agencies in the world, serving 8 million New Yorkers from ...

Job DescriptionJob Description Crowell & Moring LLP is an international law firm with offices in the United States, Europe, MENA, and Asia that represents clients in litigation and arbitration, regulatory and policy, intellectual property, and transactional and corporate matters. The firm is in...

Job Description About Figure Figure is maximizing the value of homeownership in ways that benefit consumers and the industry alike. We're helping homeowners tap their liquidity easily, efficiently and reasonably for purpose-driven, significant expenditures – everything from dream home renovation...

Job Description The position will be hybrid requiring three days per week in the office (Tues, Wed and Thurs) at our Nutley location. The position will be covering for someone on leave for 6 months. Knowledge/Skills Required • Advanced bioscience degree required (PharmD preferred), • Oncology exp...

Job Description About Cleerly We're Cleerly – a healthcare company that's revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the world's leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, mark...

Job DescriptionCompany Description EVERSANA has partnered with Mitsubishi Tanabe Pharma America, Inc. for this Direct Hire opportunity. Mitsubishi Tanabe Pharma America, Inc. (MTPA) is a U.S. subsidiary of Mitsubishi Tanabe Pharma Corporation (MTPC) in Japan, which touts a storied reputation mo...

Job DescriptionCorporate Counsel Employment Type: Full-Time Minimum Experience: 5-7 years of experience in a similar role Location: Hybrid in New York City Metropolitan Area About the Role As a fast-growing multinational enterprise, Pixalate is seeking an experienced corporate governance profess...

Job Description Company introduction: Compass Pathways plc (Nasdaq: CMPS) is a biotechnology company dedicated to accelerating patient access to evidence-based innovation in mental health. The Company is headquartered in London, UK, and has offices in New York City and San Francisco in the US. W...

This leader acts as a strategic partner to global functional line leadership across R&D (Regulatory Affairs WW Safety and Medical Digital in-country leadership and supporting functions (e. Pharmacovigilance Regulatory Medical Country & Digital Audit Strategy. Pharmacovigilance Regulatory Pfi

An Innova Solutions Client is immediately hiring for a Regulatory Guidance Specialist – Government Programs Position type: Full-time/Direct Hire Location: New York, NY (REMOTE, must be within commuting distance to NYC) Regulatory Guidance Specialist – Government Programs The Regulatory ...

An Innova Solutions Client is immediately hiring for a Regulatory Guidance Manager – Government Programs Position type: Full-time/Direct Hire Location: New York, NY (REMOTE, must be within commuting distance to NYC) Regulatory Guidance Manager – Government Programs The Regulatory Guidance Man...

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission.We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on res

HonorVet Technologies is seeking a travel nurse RN NICU - Neonatal Intensive Care for a travel nursing job in New York, New York. • Specialty: NICU - Neonatal Intensive Care, • Discipline: RN, • Start Date: ASAP, • Duration: 13 weeks, • 36 hours per week, • Shift: 12 hours, nights, • Employmen...

Prepare, submit, and manage regulatory filings across global regulatory agencies including FDA and EU submissions. As a Regulatory Affairs Lead, you will play a key role in ensuring regulatory compliance and supporting the global market expansion of products commercialized in the smart wearables ...

Develop regulatory packages and documents that meet regulatory and departmental guidelines. Provide regulatory leadership by developing, driving, and implementing regulatory strategies for assigned products. Ensure regulatory management is informed of key regulatory activities and critical issues...

Developing regulatory strategies for assigned products to optimize label and obtain shortest time to approval by regulatory agencies. Leading the Global Regulatory Teams to coordinate cross-functional regulatory support. The Associate Director, Global Regulatory Lead (GRL), will be responsible fo...

Responsibilities: The Manager, Regulatory Affairs will be responsible for managing regulatory requirements and in-market product compliance to maintain and further develop the regulatory capability of the US-based regulatory team for Alchemee. The Manager, Regulatory Affairs serves as the domesti...

ROLE SUMMARY The Global Product Counsel (GPC) for the Vaccines Franchise of Pfizer Commercial will serve as counsel to one or more of our Vaccine product teams. This GPC will provide legal guidance and counsel to commercial medical and cross-functional product teams in a matrixed corporat...

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Responsibilities: The Regulatory Affairs Consultant will be responsible for providing strategic guidance on regulatory requirements and submissions for medical devices. This role involves ensuring compliance with global regulations, preparing and managing regulatory submissions, and acting as a l...

Interact with regulatory agencies (SEC, CFTC, NFA, OCC, etc. Ideally experience with Investment Advisors/RIA from a regulatory perspective. Develop and maintain regulatory submission strategies, ensuring timely and accurate submissions.

Associate Director, Regulatory Affairs. We are seeking an experienced Senior Manager to Associate Director, Regulatory Affairs, to manage our regulatory clinical trial applications (CTAs) and compliance efforts. In this role, they will excel in developing and executing global CTA submission strat...

Independently prepare and maintain the Tracking Sheets for the global regulatory dossiers related to labelling projects in close collaboration with GLM/GL-TAL. Regulatory Labelling Documentation. Support the creation and maintenance of assigned labelling projects to enable worldwide regulatory su...

Associate Director, IT R&D Operations.The call to action to extend and improve the lives of cancer patients is louder than ever before, and Syndax is seeking individuals who are committed to science, innovation and excellence to join us on this mission.With offices in NYC and experts employed aro...

Vice President Regulatory Group.We are seeking a seasoned professional to join our Regulatory Group as a Vice President, with a primary focus on managing regulatory exams.This role is part of the Firm's Legal Department and plays a key role in ensuring regulatory compliance and oversight.While a ...

Deliver all regulatory milestones for assigned products across the product lifecycle + Identify, communicate and escalate potential regulatory issues to Organon Regulatory CMC management, as needed Required Education, Experience and Skills + Bachelor’s Degree, in a science, enginee

Prepare, submit, and manage regulatory filings across global regulatory agencies including FDA and EU submissions. As a Regulatory Affairs Lead, you will play a key role in ensuring regulatory compliance and supporting the global market expansion of products commercialized in the smart wearables ...

Collaborates with Nursing Leadership and Regulatory Affairs Leadership to develop and improve departmental, interdisciplinary, and service structure standards. Serves as a liaison between the leadership on premises and the administrator-on-call, Office of Public Affairs, Chief Medical Officer and...

Our teams include Communications, Community Impact and Investment, Community Finance, CRA Strategy and Program Management, the Government and Political Affairs Group, Regulatory Relations, and Strategy and Engagement. Community Finance builds inclusive, thriving resident-centered communities that...

Notary licensed in New York State. NewYork-Presbyterian Hospital is an equal opportunity employer. Regulatory Associate (Federal/State) Regulatory Affairs.

Europe, support of international product registrations and related regulatory affairs activities, including execution of procedures and systems designed to ensure that the product development process addresses all regulatory requirements as well. Responsibilities: This position is responsible for...

Finalize consumer-facing claims in partnership with regulatory counsel before organizational release. Manage the regulatory budget, including testing, claims validation, international registration fees, and corporate brand spend. Strategic Thinking: Ability to develop long-term regulatory strateg...

Regulatory Affairs Specialist Immigration Law. Required: Master in Law & 6-month law firm experience to perform compliance research and regulatory analysis.

Edit or manage the editing of scientific sections of regulatory documentation against the regulatory requirements. Participate in multidisciplinary project teams to provide regulatory guidance and communicate regulatory goals. Accountable for ensuring the completeness and accuracy of all regulato...

Responsibilities: In this critical role, you will lead regulatory strategies, product submissions, and a team of talented regulatory affairs professionals to drive timely product approvals and ensure ongoing regulatory compliance in key markets such as USA (FDA), EU (MDR), China (NMPA), and more....

Responsibilities: Under general supervision responsible for the coordination and the preparation of documents/packages for regulatory submissions.

Medical Devices, Regulatory Specialist. We're seeking a regulatory affairs specialist to join our medical devices compliance team. You will get to work on wearables and Software as a Medical Device (SaMD) applications for the US and worldwide approvals.

Job Description At Oura, our mission is to empower every person to own their inner potential. With our award-winning Oura Ring and app, we help over 2.5 million people turn insights about sleep, activity, and readiness into healthier, more balanced lives. We believe that starts from within — by c...

Under the direction of the Director, Medical and Regulatory Affairs, is responsible for working with key stakeholders to execute the medical affairs plan, including post-marketing research, congress management, medical education, research grants, medical advisory boards, and scientific communicat...

About the Team The Medical and Scientific Affairs, Core Lab, Regulatory and AI/Innovative Product Affairs teams share dedication and passion to release innovative products that will guide physicians to lower the number of heart attacks in their patients by providing a personalized assessment of r...

We invested in new offices, sector teams and practice groups including investor engagement; shareholder activism; governance; regulatory and public affairs, including geopolitical; crisis; litigation; social issues including climate change and diversity, equity and inclusion; cybersecurity, data ...

HonorVet Technologies is seeking a travel nurse RN Infection Control for a travel nursing job in New York, New York. • Specialty: Infection Control, • Discipline: RN, • Start Date: 08/25/2025, • Duration: 8 weeks, • 40 hours per week, • Shift: 8 hours, days, • Employment Type: Travel Job Tit...

Are you looking for a Challenge?.Looking for an innovative organization and the opportunity to learn and grow professionally? We can help! We are seeking a .Food and Drug Administration's (FDA) Office of Regulatory Affairs (ORA) Office of Regulatory Sciences (ORS) in Jamaica, NY.I've never hear

The Associate Principal Scientist (Associate Director) is responsible for developing and implementing Regulatory Chemistry, Manufacturing & Controls (CMC) strategies for assigned small molecule and/or biological products in accordance with global regulations and guidance

This position serves as a key liaison between Claims Operations, Customer Service, Regulatory Affairs, IT,Legal and other departments, proactively identifying, assessing, and mitigating compliance risks.The Analyst will monitor regulatory changes, interpret their impact on operational processes, ...

Key contributor responsible for the preparation and review of regulatory submissions consistent within global regulatory requirements and guidelines and assures complete and timely response to Health Authorities during application review. Operates in compliance with regulations, company policies,...

Job Description Job Title: Assistant Manager, Campaign Department: Health Fund Admin Reports To: Manager, Campaign FLSA Status: Exempt, Management Created: 7/1/2025 Overview of the Health Fund: The 32BJ Health Fund is a multiemployer labor-management fund that provides health ben...