164 Results for

Regulatory Affairs Jobs in Elwood, NY

Jobs

Regulatory Affairs Specialist Joulé

Trumbull, CT

$30–$35 / hour

Skills — strong communication skills, ability to manage projects with cross functional teams, proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), SAP experience helpful. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.

9 days ago

Manager, Regulatory Affairs, Advertising & Promotion Regeneron Pharmaceuticals Inc

$128,600–$210,000 / year

Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions. Provide timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs.

30+ days ago

Regulatory Affairs Specialist Regulatory Affairs Specialist Lancesoft

Trumbull, CT

Skills —strong communication skills, ability to manage projects with cross functional teams, proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), SAP experience helpful. Manage workload, priority and performance of regulatory staff, in addition to providing development opportunities to build capability.

16 days ago

Regulatory Affairs Admin Asst Life's WORC

Garden City, New York

Excellent verbal & written communication skills, excellent organizational & time management skills, as well as excellent customer service skills. Assist with follow up on incident items needed from various departments to ensure incidents are completed/closed within the regulatory timeframe.

30+ days ago

Associate Director, CMC Regulatory Affairs (Hematology/Oncology) Regeneron Pharmaceuticals Inc

Remote

$157,200–$256,600 / year

Perform final review and approval of the compliance activities of the portfolios to confirm regulatory impact and associated submission requirements for clinical and commercial regulatory filings in accordance with country-specific regulatory guidance documents; • Mentor colleagues in difficult compliance assessment discussions with SMEs or Senior Management; find opportunities for improvement of processes for compliance tasks. • Critically review and provide meaningful and strategic input on regulatory filing documents (e.g., INDs, IMPDs, meeting packages, scientific advice, BLAs, MAAs, BPDRs, annual reports, DSUR, amendments, supplements) to facilitate and expedite the development, licensure, and marketing of drugs and/or biologics.

30+ days ago

Regulatory Affairs Specialist Zobility

Trumbull, CT

Strong communication skills, ability to manage projects with cross functional teams, proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), SAP experience helpful. Work proactively with cross-functional teams to ensure product regulatory compliance and provide necessary regulatory documentation.

16 days ago

Vice President, Food Safety, Quality & Regulatory Affairs DO & CO AG

Jamaica, NY

$200,000–$230,000 / year

The ideal candidate is a transformational leader with extensive experience in multi-site food manufacturing, airline catering, commissary, or high-volume food production environments and a proven ability to build world-class food safety programs that protect consumers, strengthen customer partnerships, and uphold the integrity of the DO & CO brand. DO & CO is seeking an accomplished Vice President of Food Safety, Quality & Regulatory Affairs to provide executive leadership for all food safety, quality assurance, regulatory compliance, sanitation, supplier quality, and product integrity initiatives across our North American operations.

16 days ago

Director, Quality Systems & Regulatory Affairs (Remote - East Coast) CEFALY Technology

Darien, CT

Remote

A critical priority for this role will be optimizing and expanding the company's electronic Quality Management System (eQMS), conducting comprehensive assessments of quality documentation and system effectiveness, and driving sustainable process improvements across the organization. This role is being added to strengthen organizational quality and regulatory capabilities, reduce single-point dependency risk, improve QMS sustainability, and establish scalable systems supporting long-term growth and compliance excellence.

10 days ago

Manager, Regulatory Affairs Strategy - Immunology & Inflammation Regeneron Pharmaceuticals Inc

TARRYTOWN, NY

$128,600–$210,000 / year

A typical day might include the following: Coordinate the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development, including, but not limited to, the following: INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator's Brochure. The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures required to ensure compliance with regulations.

30+ days ago

Regulatory Affairs Specialist Globalchannelmanagement

Trumbull, CT

Strong communication skills, ability to manage projects with cross functional teams, proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), SAP experience helpful. Regulatory Affairs Specialist requires: 1-3 years experience in regulatory affairs field of Laundry and detergents or CPG products.

13 days ago

Regulatory Affairs Specialist Elliquence

BALDWIN, NY

Full time

This role collaborates cross-functionally with Quality, Engineering, Clinical, and Manufacturing teams to prepare, submit, and maintain regulatory filings with agencies such as the U.S. FDA, European Notified Bodies, and other international authorities. Create documentation in response to customer regulatory requests which includes regulatory letters, authorization letters, certifications, attestations, technical packages, etc. for tenders and for pre-market clearance.

30+ days ago

Pesticides Regulatory Affairs Specialist Globalchannelmanagement

Trumbull, Connecticut

Pesticides Regulatory Affairs Specialist needs 5 years of experience in pesticide product registration; or equivalent combination of education and experience, including preparation and submission of pesticide registration applications, product labels, offers-to-pay, data matrices, etc. Support FIFRA registrations for conventional pesticides including preparing, submitting and/or managing product applications.

13 days ago

Regulatory Affairs Specialist Lancesoft

Trumbull, CT

Skills, experience and qualifications: At least 5 years of experience in pesticide product registration;or equivalent combination of education and experience, including preparation and submission of pesticide registration applications, product labels, offers-to-pay, data matrices, etc. Responsibilities: This is work in pesticide product registration and compliance requiring an entrepreneurial attitude, and enthusiasm for supporting business development and technical efforts supporting new end-use product registrations.

16 days ago

Director, Regulatory Affairs Strategy - Genetics Medicine Regeneron Pharmaceuticals Inc

$205,000–$341,600 / year

The Director will develop and maintain regulatory strategy at the study, indication, and program level, lead interactions with global health authorities, and serve as a key cross-functional partner and subject matter expert. Working with cross-functional project teams to resolve complex regulatory issues, utilizing deep expertise in global regulations and guidances to strategically plan and communicate requirements.

20 days ago

Vice Dean of Academic Affairs, Lewyt College of Veterinary Medicine Long Island University

$220,000–$230,000 / year

Oversee agreements and collaborations with affiliates, partners, and other institutions Support the Office of Assessment Develop and manage assigned budgets Collaborates with Human Resources in faculty counseling and management of faculty grievance and appeals processes in alignment with Long Island University, Lewyt College of Veterinary Medicine mission areas. Vice Dean of Academic Affairs, Lewyt College of Veterinary MedicineVice Dean of Academic Affairs, Lewyt College of Veterinary Medicine No. 4526 Long Island University Brookville, New York Dean - Veterinary Medicine Posted Jan 23, 2026 $220,000 - $230,000.

30+ days ago

Senior Medical Affairs Strategy and Operations Specialist HealthCare Partners, MSO

Garden City, NY

$80,000–$110,000 / year

The Manager plays a critical role in facilitating leadership meetings, maintaining physician schedules, tracking strategic initiatives, preparing executive-level communications, and ensuring timely follow-through on organizational commitments. Position Summary: The Senior Medical Affairs Strategy & Operations Specialist serves as a key operational partner to the Chief Medical Affairs Officer, providing administrative, project management, and strategic execution support across the Medical Affairs division.

29 days ago

Senior Medical Director, Medical Affairs, MASH Regeneron Pharmaceuticals Inc

$333,300–$450,900 / year

This role might be for you if: • Must have an MD or MD equivalent with a preference for specialized fellowship training in Gastroenterology or Hepatology • 5 years of related industry experience in global or US medical affairs • Solid background and experience in drug development and life-cycle management • Experience with working in an alliance setting strongly preferred • Ability to lead technical and business discussions internally and externally and explain scientific/medical concepts to all levels • Ability to cultivate and maintain relationships with leading medical/scientific experts in the relevant fields • Ability to establish trust through the consistent demonstration of scientific expertise and satisfactory follow-through on requests from key opinion leaders • Strong leadership and management skills • Attention to detail in analyses, deliverables, and communications • Strong presentation and communication skills; must be able to provide succinct, strategic, and actionable insights to senior management • A proactive self-starter who can lead work and manage others independently, with the ability to see the next step and take actions without prompting • Ability to juggle multiple projects • Thorough understanding of the healthcare environment including all external stakeholders. A typical day in this role might look like: • Provides visionary leadership in the development, execution, and continuous refinement of medical strategy and tactics for assigned assets, ensuring alignment with corporate and global objectives.

30+ days ago

Government Affairs Manager Coastal Wave Recruiting

Stamford, CT

$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.

30+ days ago

Director, Influencer Marketing (Public Affairs) Orchestra

Washington, New York

$110,000–$125,000 / year

We lead integrated campaigns across media, stakeholder engagement, advocacy, research and paid media, coordinating seamlessly across internal teams and external partners to drive outcomes for clients across healthcare, nonprofits, technology, land use, education, infrastructure and other sectors. You will collaborate across public affairs, PR, digital, content, paid media and community engagement teams to build integrated programs that connect online engagement with real-world impact, including public sentiment, stakeholder alignment and policy outcomes.

30+ days ago

Athletic Student Affairs Coordinator Irvington Board Of Education

Irvington, NY

If you have not previously applied to the Irvington School District using our Applitrack system, please use the following URL, create an account and apply for the position you are seeking: New Applicants https://www.applitrack.com/irvington/onlineapp/_application.aspx?starting=true. Interested candidates should apply and utilize the Irvington Board of Education Applitrack system as follows: If you have previously applied to the Irvington School District using our Applitrack system, please use the following URL and apply for the new position you are seeking: Continue/Modify an Existing Application.

15 days ago

Principal Scientist - Clinical and Scientist Affairs Estee Lauder Inc

Melville, NY

$110,000–$125,000 / year

The company's products are sold in approximately 150 countries and territories under brand names including: Estée Lauder, Aramis, Clinique, Lab Series, Origins, M·A·C, La Mer, Bobbi Brown Cosmetics, Aveda, Jo Malone London, Bumble and bumble, Darphin Paris, TOM FORD, Smashbox, AERIN Beauty, Le Labo, Editions de Parfums Frédéric Malle, GLAMGLOW, KILIAN PARIS, Too Faced, Dr. Jart+, the DECIEM family of brands, including The Ordinary and NIOD, and BALMAIN Beauty. This individual will play a critical role in translating marketing consumer concepts into actionable and scientifically supportable data, and also translating complex scientific data into compelling product stories, ensuring scientific credibility while aligning with brand strategy and consumer expectations.

30+ days ago

SENIOR REGULATORY CONSULTANT Montefiore Medical Center

$72,000–$90,000 / year

Duties include, but are not limited to, management of clinical studies through the regulatory portion of the trial submission process, ensuring regulatory integrity of assigned clinical trials from approval to closure, develop new clinical trials and act as the main contact during the protocol development phase, correspond with the reviewing committees and personnel, assist in budget development by identifying research non-billables, and coordinate start-up meetings for new protocols. The Senior Regulatory Compliance Coordinator will act as a mentor to junior staff- providing oversight and training to multiple study teams who develop and submit documentation and information for Institutional Review Board (IRB) review and who prepare and submit documents needed for regulatory and safety reporting to sponsors and other agencies.

30+ days ago

Associate Director, Medical Affairs-Strategic Business Planning & Execution, Regeneron Pharmaceuticals Inc

$157,200–$256,600 / year

Build our future together: The Associate Director, Medical Affairs Strategic Business Planning & Execution provides project management support to the Global Medical Affairs Head and Medical Directors within our Neurology Franchise. Provide project-related process support for implementation and execution of publication and communication plans, advisory boards, expert consultations, steering committees and management of vendors.

20 days ago

Director of Regulatory and Patient Safety Stony Brook University

Stony Brook, NY

$142,800–$203,597 / year

2602444'',''2602444'',''TH Senior Staff Associate'',''TH Senior Staff Associate'',''Clinical Management'',''Clinical Management'',''US-NY-Stony Brook'',''US-NY-Stony Brook'',''JC Continued Readiness'',''JC Continued Readiness'',''Full-time'',''Full-time'',''Day Shift'',''Day Shift'',''8:30-5'',''8:30-5'',''Sat, Sun'',''Sat, Sun'',''Jul 2, 2026'',''Jul 2, 2026'',''Oct 1, 2026, 3:59:00 AM'',''Oct 1, 2026, 3:59:00 AM'',''142800 - 203597'',''142800 - 203597'','''','''',''SL5'',''SL5'',''Stony Brook University Hospital'',''Stony Brook University Hospital'',''false'',''736662'',''736662'',''true'',''736662'',''false'',''Submission for the position: Director of Regulatory and Patient Safety - (Job Number: 2602444)'',''false'',''736662'',''false'',''true''. The department will utilize the Director''s expertise to help prioritize projects, to develop detailed project plans for major safety & regulatory initiatives, assist other members of the department in planning projects, and assure a structured, well-planned approach for successful outcomes & project completion.

13 days ago

Associate Director, Regulatory Submission Project Management Regeneron Pharmaceuticals Inc

$157,200–$256,600 / year

Provides strategic oversight and leadership across therapeutic area(s), directing team members responsible for project managing regulatory milestones such as pre-IND or Scientific Advice, INDs and CTAs, BLAs, sBLAs, MAAs and Type II variations, and BLA annual reports; accountable for functional quality and consistency across the portfolio. Serves as the senior escalation point and strategic advisor for team members and cross-functional groups, resolving complex issues related to timelines, submission documents, or regulatory matters impacting the timeliness or quality of submissions; establishes best practices and process improvements to enhance functional effectiveness.

19 days ago

Senior Director Global Regulatory Lead - Oncology Eli Lilly and Co

Stamford, CT

$169,500–$248,600 / year

Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). The GRL is responsible for the creation and maintenance of the Regulatory Strategy Document (RSD) and ensures local plans, created by the regional regulatory teams, are aligned to the Global Brand Development (GBD)/global program team and business priorities in terms of the program's value proposition, workflow, product labeling, risk management, and issues management.

9 days ago

Senior Manager, Medical Affairs-Classical Hematolog Regeneron Pharmaceuticals Inc

$150,500–$245,500 / year

As a Senior Manager, Medical Affairs -Classic Hematology you will serve as a scientific and strategic resource leading the execution of our medical plans across bleeding and clotting disorders. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

30+ days ago

Regulatory Incident Reporting Analyst BetMGM

Bridgeport, CT

$64,000–$80,500 / year

This position is responsible for assisting in the investigation, drafting, and submission of incident reports concerning regulatory violations and instances of non-compliance, and for supporting the Company's efforts to ensure that its online iGaming platform, online Sportsbook, and retail Sportsbook operations remain compliant with relevant state regulations, regulatory directives, and land-based sportsbook obligations in each jurisdiction. The Regulatory Incident Reporting Analyst will work under the direction and supervision of the Senior Manager of Compliance and Incident Reporting, and will partner closely with the Senior Analyst, Regulatory Incident Reporting in the day-to-day execution of incident intake, investigation, drafting, and cross-jurisdictional fine and warning tracking workstreams.

Today

Senior Counsel, Regulatory Philip Morris International Inc

$202,400–$253,000 / year

About the role: The Senior Counsel, Regulatory provides pragmatic, solutions‑oriented legal counsel to support PMI's U.S. business by enabling regulatory‑compliant decision‑making across product strategy, data generation, commercialization, and innovation. The U.S. Food and Drug Administration has authorized versions of PMI's IQOS electronically heated tobacco devices and Swedish Match's General snus as Modified Risk Tobacco Products and renewal applications for these products are presently pending before the FDA.

30+ days ago

Digital Assets Regulatory Management Manager Deloitte Touche Tohmatsu Ltd

$144,600–$265,100 / year

Candidates joining our firm should possess an entrepreneurial drive, intellectual curiosity, creativity, and critical thinking in addition to the qualifications below: Strong oral and written communication skills, including the ability to support or lead business proposal development and sales presentations. As a Manager, you will have opportunities to: Oversee and direct end-to-end client projects focused on digital asset risk, regulatory compliance, and licensing, owning project scoping, resource allocation, timelines, quality, and deliverables.

30+ days ago

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

Stamford, CT

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).

30+ days ago

Digital Assets Regulatory Management Senior Consultant Deloitte Touche Tohmatsu Ltd

$119,000–$218,300 / year

Successful candidates will demonstrate an aptitude for complex problem-solving and analytical skills and the ability to communicate complex ideas clearly and persuasively across a variety of strategic, operational, technological, and risk management matters. Candidates joining our firm should possess an entrepreneurial drive, intellectual curiosity, creativity, and critical thinking in addition to the qualifications below: Strong oral and written communication skills, including the ability to support or lead business proposal development and sales presentations.

30+ days ago

Sr. Regulatory Manager UnitedHealth Group Inc

Westbury, NY

$91,700–$163,700 / year

The fraudulent LinkedIn messages and emails, which do not originate from any Executives LinkedIn account or of UnitedHealth Group's email domains, or those of any of its operating divisions, supposedly conducts an interview via a Zoom meeting, offers a work from home job at Optum, emails an application, sends a fake check by next day delivery through USPS and asks recipients to pay a vendor a large dollar amount. Prepare and maintain site Study binders; distribute for signatures and collect updated FDA 1572, Financial Disclosure Forms, Delegation of Authority Logs, and Training Logs.

2 days ago

Regulatory Compliance Specialist Evolution AB

Fairfield, CT

$65,000–$75,000 / year

Our live services, which allow licensees' players on desktop, tablet and smartphone to play Live Casino games at real tables and with real dealers, have won multiple industry awards, including 'Live Casino Supplier of the Year' at the EGR B2B Awards for eleven consecutive years and 'Casino Content Provider of the Year' in the 2019 EGR North America Awards. Evolution is the world´s leading provider of video-streamed Live Casino solutions and Slots, delivering best-in-class 'as real as it gets' live dealer gaming to our licensees including many of the world´s best known gaming brands.

30+ days ago

Sr. Quality Assurance Manager Prestige Consumer Healthcare Inc

$150,000–$175,000 / year

Success in this position requires strong cross-functional collaboration with internal stakeholders, including Regulatory Affairs, Medical Affairs, Strategic Sourcing, New Product Development, Package Development, Supply Planning, and Logistics, as well as the ability to influence quality outcomes across a network of third-party manufacturing partners. Evaluate the effectiveness of contract manufacturing partners quality systems by leading effective audits for cGMP compliance, issuing audit reports, managing contract manufacturing partners response adequacy and timeliness; determining system improvements.

24 days ago

Sr. Quality Assurance Manager Prestige Brands

Tarrytown, NY

Full time

22 days ago

R&D Associate (Analytical) Meds

Elmhurst, New York

We are seeking an experienced R&D Associate with expertise in developing innovative pharmaceutical formulations, performing stability and efficacy tests, and ensuring regulatory compliance. With a team of 300 professionals across various specialties, we've built scalable pharmacy, telemedicine, and e-commerce platforms using cutting-edge technology.

21 days ago

Associate Director, Biostatistics - Remote Penfield Search Partners

Fairfield, CT

Remote

This role involves overseeing CROs and collaborating with cross-functional teams to deliver high-quality analysis outputs and interpret results. You will be responsible for discussing and shaping the clinical development plan, study design, endpoint selection, statistical analysis plan, and regulatory submission and publication strategy to support pursuant of precision medicine.

29 days ago

Consultant - Product Quality & Safety - Life Sciences & Healthcare Deloitte Touche Tohmatsu Ltd

$88,700–$170,900 / year

Support implementation and optimization of systems such as eQMS, document management systems, learning management systems, complaint handling, CAPA, change control, audit management, supplier quality, and regulatory information management platforms. The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs.

30+ days ago

Manager, Product Engineering (Research & Development) The Cooper Companies Inc

Trumbull, CT

Interfaces cross-functionally with R&D, Quality, Regulatory Affairs, Operations, Marketing, and external suppliers to deliver product enhancements, address field issues, and ensure ongoing product reliability and compliance. All resumes submitted by search firms/employment agencies to any employee at CooperSurgical via-email, the internet or in any form and/or method will be deemed the sole property of CooperSurgical, unless such search firms/employment agencies were engaged by CooperSurgical for this position and a valid agreement with CooperSurgical is in place.

30+ days ago

Director Medical Governance and Compliance PepsiCo Inc

Purchase, NY

$132,200–$262,400 / year

In addition to salary, PepsiCo offers a comprehensive benefits package to support our employees and their families, subject to elections and eligibility: Medical, Dental, Vision, Disability, Health, and Dependent Care Reimbursement Accounts, Employee Assistance Program (EAP), Insurance (Accident, Group Legal, Life), Defined Contribution Retirement Plan. This role establishes and oversees the quality framework that enables unbranded, science‑centric engagement, evidence generation, and external scientific collaboration in a compliant and scalable manner.

30+ days ago

Staff Attorney - Tarrytown ENT and Allergy Associates

White Plains, New York

Each ENT and Allergy Associates clinical location provides access to a full complement of services, including General Adult and Pediatric ENT, Voice and Swallowing, Facial Plastics and Reconstructive Surgery, Disorders of the Inner Ear and Dizziness, Asthma, Clinical Immunology, Diagnostic Audiology, Hearing Aid dispensing, Sleep and CT Services. ENTA has a clinical alliance with The Mount Sinai Hospital for the treatment of diseases of the head and neck and esophageal cancer and a partnership with the American Cancer Society to educate and treat patients with smoking disorders and cancer.

30+ days ago

Associate Director, Clinical Diagnostics Regeneron Pharmaceuticals Inc

Armonk, NY

$176,100–$287,300 / year

This role drives cross-functional alignment across biomarker science, clinical development, regulatory, commercial, and external IVD partners to deliver fit-for-purpose assays that meet global regulatory requirements and support clinical decision-making. You will lead the CDx portfolio from early biomarker feasibility through clinical validation, registration, launch, and post-market sustainment, ensuring timely availability of high-quality diagnostics aligned with drug development milestones.

30+ days ago

Senior Counsel St. Catherine of Siena Medical Center

Rockville Centre, NY

$265,000–$300,000 / year

Population Health and value-based care, including providing legal guidance and operational support to the Catholic Health population health entities, drafting and negotiating value-based arrangements, and providing legal advice regarding federal and state population health initiatives including Accountable Care Organizations, Team Model participation, Medicaid 1115 Waiver initiatives and alternate payment models and value-based contracting arrangements. The Senior Counsel will manage and carry out legal work, including but not limited to the following areas of legal practice: Corporate and transactional matters, including providing legal counsel and strategic guidance regarding business initiatives, affiliations, mergers, acquisitions, joint ventures and restructurings.

30+ days ago

Senior Counsel Catholic Health

Rockville Centre, New York

$265,000–$300,000 / year

Population Health and value-based care, including providing legal guidance and operational support to the Catholic Health population health entities, drafting and negotiating value-based arrangements, and providing legal advice regarding federal and state population health initiatives including Accountable Care Organizations, Team Model participation, Medicaid 1115 Waiver initiatives and alternate payment models and value-based contracting arrangements. The Senior Counsel will serve as a key member of the Office of General Counsel and provide strategic legal guidance and operational support across a broad range of healthcare regulatory, transactional, corporate, population health, physician, compliance, and privacy matters.

30+ days ago

Senior Counsel Mastercard Inc

Purchase, NY

$204,000–$325,000 / year

All activities involving access to Mastercard assets, information, and networks comes with an inherent risk to the organization and, therefore, it is expected that every person working for, or on behalf of, Mastercard is responsible for information security and must: Abide by Mastercard's security policies and practices; Ensure the confidentiality and integrity of the information being accessed; Report any suspected information security violation or breach, and. Work cross-functionally with various product and legal teams, including data privacy, intellectual property, anti-trust, regulatory affairs, public policy, and franchise functions to provide holistic support to Mastercard's global and regional products strategy.

30+ days ago

Data Engineer Lead- PMS & QA The Cooper Companies Inc

Trumbull, CT

$120,000–$160,000 / year

Scope: The Data Engineer Lead - PMS & QA leads data analysis, visualization, and reporting of Medical Device performance and Post Market Surveillance activities within the PMS team as well as the broader QA function and supports CooperSurgical Complaint Management and other Quality areas by working in partnership with Commercial, Operations, Regulatory Affairs and Post Market Surveillance teams. This role helps to ensure on-going regulatory compliance and continuous product & process improvements within PMS & QA and supports CooperSurgical Complaint Management and other Quality areas by working in partnership with our Commercial, Operations (QA & Manufacturing), Regulatory Affairs and Post Market Surveillance teams.

30+ days ago

Managed Services Sr. Consultant Deloitte Touche Tohmatsu Ltd

$120,200–$140,000 / year

Lead and contribute to end-to-end delivery for Generis CARA and associated regulatory technology platforms - including requirements gathering, solution design, system configuration, content template development, and user acceptance testing. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities.

30 days ago

Patient Safety Officer Montefiore Medical Center

Yonkers, NY

$225,000–$350,000 / year

Aggregate, analyze and interpret safety data (including serious safety events, never events, electronic trigger tools, and voluntary error reports) identifying trends, root causes, and opportunities for improvement; communicate findings and action plans to senior leadership; drive improvements to ensure best-in-class safety. Reporting to the Chief Quality Officer with a strong connection to the System Chief Medical Officer, this role will serve as a central figure in advancing patient safety across our organization, overseeing the work of the regulatory, quality management, peer-review, and patient safety improvement teams.

30+ days ago

Process Engineer Perrigo Co Plc

Bronx, NY

$95,000–$120,000 / year

The Process Engineer is responsible for supporting product scale-up activities, evaluating manufacturing and product performance, investigating deviations and product failures, and implementing effective corrective and preventive actions to ensure product quality, compliance, and operational excellence. Lead technology transfer activities for newly developed products and transferred manufacturing processes from R&D or external manufacturing sites into commercial operations, ensuring successful scale-up and implementation.

5 days ago

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Regulatory Affairs Jobs in Elwood, NY

Regulatory Affairs Specialist Joulé

Manager, Regulatory Affairs, Advertising & Promotion Regeneron Pharmaceuticals Inc

Regulatory Affairs Specialist Regulatory Affairs Specialist Lancesoft

Regulatory Affairs Admin Asst Life's WORC

Associate Director, CMC Regulatory Affairs (Hematology/Oncology) Regeneron Pharmaceuticals Inc

Regulatory Affairs Specialist Zobility

Vice President, Food Safety, Quality & Regulatory Affairs DO & CO AG

Director, Quality Systems & Regulatory Affairs (Remote - East Coast) CEFALY Technology

Manager, Regulatory Affairs Strategy - Immunology & Inflammation Regeneron Pharmaceuticals Inc

Regulatory Affairs Specialist Globalchannelmanagement

Regulatory Affairs Specialist Elliquence

Pesticides Regulatory Affairs Specialist Globalchannelmanagement

Regulatory Affairs Specialist Lancesoft

Director, Regulatory Affairs Strategy - Genetics Medicine Regeneron Pharmaceuticals Inc

Vice Dean of Academic Affairs, Lewyt College of Veterinary Medicine Long Island University

Senior Medical Affairs Strategy and Operations Specialist HealthCare Partners, MSO

Senior Medical Director, Medical Affairs, MASH Regeneron Pharmaceuticals Inc

Government Affairs Manager Coastal Wave Recruiting

Director, Influencer Marketing (Public Affairs) Orchestra

Athletic Student Affairs Coordinator Irvington Board Of Education

Principal Scientist - Clinical and Scientist Affairs Estee Lauder Inc

SENIOR REGULATORY CONSULTANT Montefiore Medical Center

Associate Director, Medical Affairs-Strategic Business Planning & Execution, Regeneron Pharmaceuticals Inc

Director of Regulatory and Patient Safety Stony Brook University

Associate Director, Regulatory Submission Project Management Regeneron Pharmaceuticals Inc

Senior Director Global Regulatory Lead - Oncology Eli Lilly and Co

Senior Manager, Medical Affairs-Classical Hematolog Regeneron Pharmaceuticals Inc

Regulatory Incident Reporting Analyst BetMGM

Senior Counsel, Regulatory Philip Morris International Inc

Digital Assets Regulatory Management Manager Deloitte Touche Tohmatsu Ltd

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

Digital Assets Regulatory Management Senior Consultant Deloitte Touche Tohmatsu Ltd

Sr. Regulatory Manager UnitedHealth Group Inc

Regulatory Compliance Specialist Evolution AB

Sr. Quality Assurance Manager Prestige Consumer Healthcare Inc

Sr. Quality Assurance Manager Prestige Brands

R&D Associate (Analytical) Meds

Associate Director, Biostatistics - Remote Penfield Search Partners

Consultant - Product Quality & Safety - Life Sciences & Healthcare Deloitte Touche Tohmatsu Ltd

Manager, Product Engineering (Research & Development) The Cooper Companies Inc

Director Medical Governance and Compliance PepsiCo Inc

Staff Attorney - Tarrytown ENT and Allergy Associates

Associate Director, Clinical Diagnostics Regeneron Pharmaceuticals Inc

Senior Counsel St. Catherine of Siena Medical Center

Senior Counsel Catholic Health

Senior Counsel Mastercard Inc

Data Engineer Lead- PMS & QA The Cooper Companies Inc

Managed Services Sr. Consultant Deloitte Touche Tohmatsu Ltd

Patient Safety Officer Montefiore Medical Center

Process Engineer Perrigo Co Plc

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