281 Results for

Regulatory Affairs Jobs in Taurus, NJ

Jobs

Basking Ridge, NJ9 days ago

$184,240–$276,360 Per Year
Full-time

The Director, Regulatory Affairs Advertising and Promotion (RAAP) provides senior strategic and tactical regulatory leadership for U.S. promotional and selected non-promotional communications across assigned products, therapeutic areas, and key business initiatives within the Daiichi Sankyo portfolio, including alliance assets. Interpret evolving FDA regulations, guidances, enforcement trends, compliance letters, and relevant industry developments, including ambiguous or precedent-setting issues, and translate them into actionable regulatory strategy and business guidance.

Warren, NJ13 days ago

This individual serves as the regulatory affairs main contact to project teams, providing leadership across functions for regulatory strategic planning and execution related to achieving program milestones. Oversees the day-to-day operations within the regulatory affairs function including oversight of submission coordination, submission publishing, advertising/promotional review, and process development/improvement initiatives.

Basking Ridge, NJ11 days ago

$116,400–$174,600 Per Year
Full-time

Acting as QA point person for assigned programs, the Manager collaborates with GxP Quality representatives (Development QA, Audits & Compliance, Quality Management System (QMS) QA including Vendor Quality, Pharmacovigilance QA and provides guidance during the development and execution of Corrective and Preventive Actions (CAPAs), including tracking timely closure, effectiveness checks, and escalation of critical issues. Serve as a key liaison to support audits and inspections as applicable Cross-functional and Global Team Participation: Participate in the review of quality and compliance topics, including KQI, at Quality Governance Meetings, in close alignment with DS QA teams (DSJ, DSI, DSE, DSBR) to proactively identify potential risks and opportunities for continuous improvement.

New!

New York, NY4 days ago

$350,000–$400,000 Per Year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. 4. Collaborate with cross-functional teams including regulatory affairs, pharmacovigilance, and medical affairs to ensure a holistic approach to product development.

Long Island City, NY23 days ago

$48,647–$59,444 Per Year
Full-time
Employee

CREAR (College Readiness, Achievement, and Retention) Futuros—meaning “to create futures”—is a national, Hispanic Federation–powered peer mentorship initiative designed to promote college access, retention, academic success, leadership development, and graduation among Latinx students, while remaining open to all eligible students regardless of background. At LaGuardia Community College, CREAR Futuros is housed within Casa de las Américas, a student-centered cultural and academic hub advancing the educational, professional, and leadership development of Latinx, Latin American, and Caribbean students through high-impact and culturally informed programming.

New!

Totowa, NJ1 day ago

$90,000–$100,000 Per Year

The successful candidate will provide quality assurance management, decision making, and support to the RCM group with specific emphasis on change control, corrective and preventive actions, procedure approval, exception reporting, partner/sponsor communications, validation and qualification reviews, and review and approval of various other documents and reports applicable to new products. This includes making quality related decisions and assisting in the generation, review, and approval of change controls, corrective and preventive actions, procedures, exception reports, protocols, and other documents applicable to new products.

Basking Ridge, NJ11 days ago

$153,600–$230,400 Per Year
Full-time

Provide oversight of ICSR processing activities including, Safety Information submission to Health Authorities and License Partners, Reconciliation with License Partners, Patient Support Programs, Market Research vendors, Global Quality Supply Chain, Medical Information Social Media and other suppliers. Oversees Local/Global Pharmacovigilance (PV) service providers responsible for Call Center, individual safety case processing, and aggregate reporting for DSI products, both investigational and marketed.

Basking Ridge, NJ11 days ago

$242,700–$404,500 Per Year
Full-time

Lead scientist team to collaborate with safety physicians, regulatory affairs, clinical development, other functions and external partners to deliver high-quality safety assessments, regulatory submissions, aggregate reports, and responses to health authority queries. In addition to operational oversight, this role contributes to the development of global safety processes, talent capability building, and strategic alignment across the broader Clinical Safety and Pharmacovigilance (CSPV) function and the enterprise.

New!

New York, NY4 days ago

$180,000–$350,000 Per Year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. We are a leading AM 100 Law Firm specializing in corporate and business law, complex litigation, intellectual property, regulatory matters, and government affairs and employing some of the best and brightest attorneys.

New York, NY7 days ago

$35–$41

This position will primarily support hiring for Resource Development, Marketing, and Communications teams, including roles within Development/Fundraising, Public Affairs, Corporate Communications, and Marketing & Communications. Determining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to: the individual’s skill sets, experience and training; licensure and certification requirements; office location and other geographic considerations; other business and organizational needs.

Basking Ridge, NJ11 days ago

$175,440–$263,160 Per Year
Full-time

This role will influence the external policy landscape so the value of Daiichi Sankyo's pipeline, portfolio, and business is protected and enhanced – allowing Daiichi Sankyo to continue bringing innovative medicines to patients who need them. Leverage subject matter expertise to assess potential policy implications to Daiichi Sankyo with internal stakeholders (e.g., Market Access, Regulatory Intelligence, etc.), develop DSI policy strategies and shape policy reform.

New!

Basking Ridge, NJ3 days ago

$228,160–$342,240 Per Year
Full-time

Work in an exciting and challenging legal environment by independently providing innovative and strategic legal support and solutions as a brand attorney and the primary legal advisor for the commercial business and operations supporting U.S. approved (or to be approved) oncology products and to specific assigned business functions in the Oncology Business Unit/US Oncology Business Division (including, for example, Medical Affairs, Sales, Marketing, etc.) including, but not limited to, areas of vendor agreements, legal, business and regulatory issues. 7 or More Years pharmaceutical industry experience, particularly supporting specific assigned products and business areas in contracting, general legal advice, policy development and/or review, etc. in specific business support functions in an in-house capacity, as a legal consultant, and/or at a law firm in a practice group focusing on pharmaceutical industry and/or specific corporate business functions preferred .

Brooklyn, NY13 days ago

PAGNY is one of the largest physician groups in the country and directly employs nearly 4,000 physicians and allied health professionals who provide services to NYC Health + Hospitals, the largest municipal health care system in the nation serving more than a million New Yorkers annually. Located in the heart of Brooklyn, Kings County Hospital accommodates more than 518,076 outpatient visits, more than 141,328 emergency room visits, 627 beds, and more than 25,000 inpatient admissions annually.

New!

Rahway, NJ1 day ago

$45–$53.45 Per Hour

Serve as a subject matter expert in immunoassay-based assay development and validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical trials. Translational Molecular Biomarkers (TMB) is responsible for the development and execution of clinical biomarker assays across all therapeutic areas and all phases of clinical development within our company's research laboratories.

Clark, NJ30+ days ago

This role will focus on reviewing product formulas and artwork for regulatory compliance, supporting product notification and registration processes, and maintaining documentation related to regulatory requirements. Compensation: The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more.

New York City, NY30+ days ago

Remote

$79,488–$104,328 Per Year

Manage the end-to-end administrative lifecycle of each dispute by maintaining real-time updates on project management boards, gathering and redacting member documentation, and uploading supporting evidence to the appropriate portal stages within set regulatory deadlines. Work Location: This is a remote position, open to candidates who reside in: Arizona, Florida, Georgia, Illinois, Iowa, Kansas, Michigan, Missouri, Nebraska, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Tennessee, Texas and Virginia.

New York City, NY30+ days ago

Remote

$160,000–$215,000 Per Year

Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Axsome Therapeutics does not accept unsolicited resumes from recruiters or third-party recruitment agencies and will not pay placement fees for unsolicited candidates that are sent to hiring managers, the HR team or other Axsome team members.

Warren, NJ30+ days ago

$190,000–$220,000 Per Year

This individual serves as the regulatory affairs main contact to project teams, providing leadership across functions for regulatory strategic planning and execution related to achieving program milestones. By providing your phone number, you consent to: (1) receive automated text messages and calls from the Judge Group, Inc. and its affiliates (collectively "Judge") to such phone number regarding job opportunities, your job application, and for other related purposes.

Cranbury, New Jersey30+ days ago

$360,000–$400,000 Per Year

Advises leadership team and Board on regulatory strategy and execution for early and late-stage programs, CMC, nonclinical and commercial activities, as well as advice on areas of regulatory risk, and updates on new governmental/regulatory developments. As the company continues to scale, the incumbent will have the ability to contribute to the organizational build and directly impact patients’ lives by gaining approval for, and delivering on, critical gene therapy products for rare and undertreated diseases.

New York, NY30+ days ago

Full-time

As the public policy environment globally is evolving rapidly due to technological change and a desire by policymakers to drive economic growth and international competitiveness, you will provide support to the CIB Regulatory Affairs team in responding to this dynamic environment and feed into the firm's advocacy, engagement, and strategic responses on key regulatory policy issues. Our history spans over 200 years and today we are a leader in investment banking, consumer and small business banking, commercial banking, financial transaction processing and asset management.

Jersey City, NJ15 days ago

The Senior Director will represent Company in key stakeholder and strategy meetings on regulatory matters related to medical product development and commercialization, including meetings with executive leadership, meetings with the Food and Drug Administration (FDA) and other regulators. The Senior Director, Regulatory Affairs is responsible for providing subject matter expertise on matters related to global regulatory activities, as well as providing leadership for the growth and responsibilities of the regulatory department.

Monmouth Junction, New Jersey30+ days ago

Essenlix Corporation is a fast-growing medical device company focused on developing innovative point-of-care (POC) diagnostic systems, including hematology analyzers and disposable cartridges for complete blood count (CBC) testing. We are seeking an experienced Senior Regulatory Affairs & Quality Systems Manager to lead FDA 510(k) and CLIA submissions and global quality system development.

Brooklyn, NY30+ days ago

$100,000–$125,000 Per Year

Prioritize the highest-leverage advocacy opportunities and initiatives related to grid modernization, integrated resource planning, demand-side management, transportation electrification, energy storage, rate cases, state and federal legislation and grant programs, etc. Work with the latest technologies: You'll gain exposure to a broad spectrum of IoT, SaaS and machine learning obstacles, including distributed fault-tolerance, device control optimization, and process modeling to support scalable interaction with disparate downstream APIs.

New!

New York, NY3 days ago

$110,000–$230,000 Per Year

Oversee all facets of compliance-related regulatory exams, as well as additional exams covering other Independent Risk Management (IRM) functions, such as Operational Risk Management, etc., as requested by CRO; manage exam requests, meeting preparation and presentation, exam logistics, and communication of exam deadlines and updates to relevant parties, and Senior and Executive Management; and ensure efficient, effective and accurate communication between regulators and the Bank. The VP establishes and maintains RAO policies/procedures and oversees all Regulatory Affairs Matters, including project management, stakeholder relationships, and day-to-day processes, communication with regulators, tracking and coordinating regulatory deliverables, driving the submission process to ensure timely execution and quality assurance, and reporting regulatory updates to Bank Management and committees.

Parsippany, New Jersey18 days ago

Establish and oversee formal processes to provide regulatory support in the development, revision, review, and approval of labeling content for submission to Health Authorities (USPI, EU PI, and ROW labeling, as well as the internal Company Core Data Sheet). The range considers a wide range of factors that are considered in making compensation decisions, including but not limited to: geographic markets, business or organizational needs, skill sets, experience, training, licensure, and certifications.

New!

New York, New York3 days ago

Remote

$1,150–$1,450

Include design history files, regulatory submissions, DHF/DMR documents, risk-analysis matrices, validation protocols, CAPA records, and email threads. Task Completion Pay: Competitive and based on task quality (~$1,150–$1,450 per completed task).

Madison, NJ30+ days ago

$207,490–$251,433 Per Year

This individual will be involved in integrated strategic planning within Global Medical Affairs under the direction of the US Medical Multiple Myeloma lead and Global Multiple Myeloma disease lead as well as in close partnership with the US Commercialization organization, Clinical Research and Development, HEOR, Market Access, Translational Development, and Regulatory, and will lead the US Medical asset strategy supporting the US and Global Multiple Myeloma Disease Leads. Provide high quality clinical input and review of congress abstracts, posters, presentation slides, manuscripts, educational materials, steering committee and advisory board meeting materials, medical information response documents, scientific educational grant requests, compassionate use requests, and patient advocacy grant requests among others.

Hicksville, NY30+ days ago

Full-time

Seeking a motivated, intelligent and hard-working individual to Develop and maintain quality and regulatory compliance in Genadynes' processes. Maintaining the effectiveness of quality control system and non-conforming materials control system.

New York, NY20 days ago

$175,000–$225,000 Per Year

Reporting to the Chief Medical Officer, this leader will elevate Cellectis’ scientific presence, support pipeline advancement, and ensure medical excellence in evidence generation, scientific communications, and external engagement. Cellectis is seeking a highly experienced Senior Director, Medical Affairs to help shape and operationalize the company’s medical affairs strategy across its clinical‑stage portfolio.

Paramus, New Jersey25 days ago

Qualifications: Bachelor’s degree required, advanced degree strongly preferred (eg, PharmD, PhD, MD), 10+ years experience in Medical Affairs with Bachelor’s degree; 8+ years of experience with advanced degree; experience in the therapeutic area of Neuroscience/CNS is highly preferred, Prior experience in analytics, business intelligence, or related function within the pharmaceutical or biotech industry is preferred, Prior experience in MSL operations, including analytics of field scientific interactions, is preferred, Experience with visualization tools (e.g., Tableau) and CRM systems (e.g., Veeva). Overview: The Senior Director, Medical Affairs Insights & Field Operations, is responsible for supporting a high-performance Medical Science Liaison (MSL) team through strategic planning, performance analytics, and the development of scientific content related to our product, pipeline, and disease state education.

Hackensack, New Jersey30+ days ago

Overview: The Transition APN Per Diem, Medical Affairs utilizes a patient-centered coordinated care model, demonstrating competencies in leadership, direct clinical practice, consultation/collaboration, coaching/guiding, research, and ethical decision-making. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.

Summit, NJ26 days ago

$40–$47 Per Year
Temporary
Contractor
Full-time

Support the shaping and lead the execution of Neutrogena Makeup communication campaigns, partnering with multifunctional teams and leading creative and influencer agencies to deliver campaigns that drive mental availability for the brand and platform. The Brand Manager for Global Makeup is responsible for identifying and executing innovation, claims and communications required to drive global growth on the Makeup platform.

Parsippany, New Jersey30+ days ago

$120,000–$165,000 Per Year

This role is responsible for building and scaling project management capabilities and frameworks for strategic initiative execution, enabling leadership to track program progress and provide transparent visibility into project status, timelines, risks, and critical path activities across Clinical Affairs bridging clinical and commercial planning functions to support data-driven decision-making. Project Manager, Medical Affairs provides strategic oversight and expert project management across the full lifecycle of clinical programs, ensuring alignment, efficiency, and delivery excellence across Clinical Affairs subfunctions, including Clinical Development Operations, Publications, HEOR, Pharmacovigilance, and Late-Stage Research.

Summit, NJ17 days ago

$30–$35 Per Year
Full-time
Employee

Work closely with cross-functional teams, including other R&D functions, Commercial Marketing, Quality Assurance, Regulatory Affairs, and Manufacturing, to achieve project goals. Prepare and maintain detailed documentation for product development processes, including experimental protocols, and technical reports in compliance with Good Documentation Practices (GDP).

Piscataway, NJ30+ days ago

$124,000–$174,000 Per Year

This high-impact role, sitting within the Global Consumer Affairs Team, reporting to the Senior Director of Global Consumer Affairs, is critical to the functional transformation of our worldwide Consumer Affairs organization, ensuring our technology strategy is flawlessly aligned and executed to provide a compliant, efficient, and best-in-class consumer experience across all divisions. + Technical competency: Ability to translate business needs into technical requirements, manage SaaS vendors and IT partners, understand APIs/integrations at a working level and govern change processes (SLAs, root cause, CAPA, validation readiness).

Piscataway, NJ30+ days ago

$124,000–$174,000 Per Year

This high-impact role, sitting within the Global Consumer Affairs Team, reporting to the Senior Director of Global Consumer Affairs, is critical to the functional transformation of our worldwide Consumer Affairs organization, ensuring our technology strategy is flawlessly aligned and executed to provide a compliant, efficient, and best-in-class consumer experience across all divisions. Technical competency: Ability to translate business needs into technical requirements, manage SaaS vendors and IT partners, understand APIs/integrations at a working level and govern change processes (SLAs, root cause, CAPA, validation readiness) .

New York City, NY30+ days ago

$198,720–$260,820 Per Year

You will manage a third-party vendor responsible for building and operating a new national coalition, you will ensure alignment between coalition activity and Oscar's federal and state policy and advocacy objectives, you will translate complex healthcare and technology policy issues into coordinated advocacy and thought-leadership initiatives among a diverse group of external stakeholders. Designs and maintains the strategic framework for Oscar's external coalition; define mission, membership criteria, governance structure, messaging pillars, and policy priorities in alignment with Government Affairs colleagues, communications partners, and key internal business and strategy stakeholders.

Totowa, NJ30+ days ago

Full-time

Responsibilities: The General Affairs & Operations Specialist - Manager is responsible for providing strategic oversight of the company's operational infrastructure and non-payroll expenditures through a variety of tasks, including:Operational Support & Office ManagementOversee day-to-day office operations, including space planning, office supplies procurement, and mail/logistics management to ensure a seamless work environment. The General Affairs & Operations Specialist - Manager provides strategic operational oversight by managing the company’s non-payroll expenditure, physical infrastructure, and contractual ecosystem.

White Plains, NY30+ days ago

Whether building technology to make our hospitals more efficient, recruiting and growing incredible VEGgies, or bringing our brand to life through marketing, our VQ (VEG Headquarters) team makes it all possible—ensuring our hospitals and people have everything they need to help pets and their families. Strategic Legal Partnership: Serve as a trusted advisor to VEG's business and clinical teams by delivering proactive, business-minded legal guidance that enables smart, fast decision-making.

Stamford, CT26 days ago

$125,000–$150,000

This is a high-impact opportunity for a government affairs leader who can balance strategic thinking with hands-on execution to influence public policy outcomes and protect long-term business interests. Our client, a global consumer products company, is seeking a Government Affairs Manager to lead the development and execution of a comprehensive government affairs strategy aligned with corporate goals and priorities.

Yonkers, NY7 days ago

REQUIRED QUALIFICATIONS: The successful candidate must possess one of the following: A Master's Degree in Education, Educational Administration, Public Administration, Business Administration or a related field and a minimum of two years of experience in the administration of an academic, programmatic or support services area in the field of Education or in the public sector; OR . The Division Coordinator establishes and maintains effective working relationships with internal and external entities, and serves as a primary administrative liaison to vendors and providers, ensuring clear communication, timely issue resolution, and alignment with contractual and funding requirements.

New!

New York, New York3 days ago

Remote

$1,150–$1,450

Annotate, label, and validate data across compliance use cases like control testing and regulatory change management. Create realistic scenarios based on compliance and risk workflows such as regulatory examinations and internal audit findings.

Montville, NJ18 days ago

$115,000–$155,000 Per Year

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. Conduct global risk assessments, interpret complex multi-regional requirements, and develop strategies to mitigate regulatory risks.

New York City, NY30+ days ago

$163,944–$215,176 Per Year

The Director, Corporate and Regulatory Compliance is responsible for designing, implementing, training, investigating, monitoring, and enforcing, when necessary, programs, policies, and practices to ensure all applicable operational functions are in compliance with and maintains compliance with federal, state and local regulatory requirements. In collaboration with the Legal and Government Affairs functions, manage Oscar's relationship with various regulatory entities in order to facilitate tech-driven innovation, remediate identified noncompliance, and meet or exceed Compliance Program Effectiveness requirements.

New York, NY30+ days ago

Full-time

The group is responsible for managing regulatory examinations, reviews, continuous monitoring, inquiries, horizon scanning for emerging regulations, regulatory change management, maintenance of the laws, rules and regulations library, firmwide regulatory projects and other regulatory-related matters. The Regulatory Affairs Group is seeking a Vice President of Regulatory Change Management who will lead the horizon scanning process to identify upcoming regulatory changes, analyze requirements to determine downstream implications and communicate assessments to impacted stakeholders.

Hackensack, NJ30+ days ago

The client is in search of a Quality and Regulatory Manager to join our growing team, responsible for the management and execution of day to day Quality and Regulatory systems. KEY RESPONSIBILITIES:Manage and execute daily QA and Regulatory activities including Change Control, Document Control, Deviations/Non-Conformances, CAPAs, Supplier Management.

New York, NY30+ days ago

Full-time

Responsibilities include, but not limited to, setting up exam SharePoint site, drafting regulatory responses with stakeholders, developing briefing materials and regulatory meeting presentation materials, taking meeting minutes, setting up internal preparation meetings and tracking regulatory requests and firm's responses. Responsibilities include, but not limited to, drafting Management Response Letter and remediation plan with stakeholders, developing regulatory meeting presentation materials, taking meeting minutes, setting up internal meetings and tracking and monitoring milestones.

Stamford, CT30+ days ago

Full-time

10+ years of progressive experience in regulatory reporting, excise/compliance operations, licensing, or regulatory tax operations, 5+ years of experience working in a highly regulated nicotine/tobacco environment (smokeless tobacco, modern oral nicotine pouches, heated tobacco, ENDS, or adjacent regulated consumer goods). Position Overview: The Senior Manager, Regulatory & Compliance Reporting leads U.S. federal and state tobacco/nicotine regulatory reporting and the full lifecycle of tax-related licensing and permits for a multi-entity, multi-site smoke-free and smokeless portfolio (e.g., nicotine pouches, traditional smokeless tobacco, heated tobacco).

New!

Madison, NJ6 days ago

$65–$68 Per Hour

Summary Reporting to the Program Management Lead, the incumbent willbe part of the late development translational group based in Giralda Farms NJ and will be responsible for writing scientific documents including biomarker reports, regulatory documents (eg, non-clinical summaries, translational portions of clinical/pharmacology summaries, briefing books, CSRs, investigator brochures) in conjunction with Translational scientists. Strong verbal and written communication skills with experience in developing written documents such as primary manuscripts/publications/reviews, disease strategies, mechanism slides, regulatory submissions, strategic communications, literature/market/pt segment analyses.

Summit, NJ30+ days ago

2. Prepare and review CMC submission documents, registration dossiers, health authority briefing packages and responses to health authorities through collaborations with relevant line functions and with minimal supervision. Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions.

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Regulatory Affairs Jobs in Taurus, NJ

Director, Regulatory Affairs Advertising and Promotion Daiichi Sankyo, Inc.

Director, Regulatory Affairs Strategy Aquestive Therapeutics

Manager, Medical Affairs Quality, RD PV QA Daiichi Sankyo, Inc.

Vice President Clinical Development Ophthalmology Jobot

CREAR Futuros Program Coordinator (Academic Program Coordinator) LaGuardia Community College

Quality Manager, Partners SOFIE

Associate Director, PV Strategic Partner Management Daiichi Sankyo, Inc.

Senior Director, Clinical Safety Scientist Daiichi Sankyo, Inc.

Transactional Construction Associate Attorney Jobot

Talent Acquisition Specialist Vaco LLC

Associate Director, Public Policy Daiichi Sankyo, Inc.

Assistant General Counsel Commercial Daiichi Sankyo, Inc.

Associate Director, Patient Safety and Risk Management - NYC Health + Hospitals/Kings County - Brooklyn, New York Physician Affiliate Group of New York

Scientist - II Nesco Resource

Regulatory Affairs Associate I IntelliPro Group Inc.

Senior Analyst, Regulatory Affairs Oscar Health

Associate Director/Director, Regulatory Affairs Axsome Therapeutics

Director, Regulatory Affairs Strategy Judge Group

Senior Vice President, Regulatory Affairs Rocket Pharmaceuticals

Associate, Regulatory Affairs - Global Government Relations JPMorgan Chase Bank, N.A.

Senior Director, Regulatory Affairs Clinical Dynamix, Inc.

Senior Regulatory Affairs & Quality Systems Manager - IVD / FDA 510(k) Essenlix

Manager, Policy and Regulatory Affairs EnergyHub

Legal & Compliance Department-Regulatory Affairs Office (RAO) AVP/VP Bank of China Limited, New York Branch

Senior Director, Regulatory Affairs Advertising, Promotion, & Labeling Pacira Pharmaceuticals, Inc.

Regulatory Affairs Expert - Fully Remote Mercor

Director, US Medical Affairs, Multiple Myeloma Bristol Myers Squibb

Regulatory Affairs/Quality Assurance Engineer Genadyne Biotechnologies

Senior Director, Medical Affairs Cellectis

Senior Director, Medical Affairs Insights & Field Operations SK Life Science, Inc.

Transition APN Per Diem, Medical Affairs Hackensack Meridian Health

Global Brand Manager YANTRAN LLC

Sr. Project Manager (Medical Affairs) Pacira Pharmaceuticals, Inc.

Research & Development, Scientist 2 YANTRAN LLC

Consumer Affairs Global Systems & Ops Manager Colgate-Palmolive

Consumer Affairs Global Systems & Ops Manager (Piscataway, NJ, US) Colgate-Palmolive Company

Director, Public Affairs Oscar Health

General Affairs & Operations Specialist - Manager - Cosmetics & Skincare Englewood Lab, Inc.

Senior Director, Legal Affairs Veterinary Emergency Group (VEG)

Government Affairs Manager Coastal Wave Recruiting

Division Coordinator (CC-EXT) - WEOC Business Affairs SUNY Westchester Community College

Regulatory Compliance Expert - Risk Specialist Mercor

Global Regulatory Compliance Manager Joulé

Director, Corporate and Regulatory Compliance Oscar Health

Regulatory Change Management Mizuho Americas Services LLC

Quality and Regulatory Manager CEDENT

Regulatory Relations Mizuho Americas Services LLC

Sr. Manager, Regulatory & Compliance Reporting Philip Morris International U.S.

Nonclinical Regulatory Document and Scientific Writer sunrise systems

Scientific - Global Regulatory CMC Manager TechDigital Corporation

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