Director, Regulatory & Administrative Affairs - Institute for Transformative Clinical Trials Mount Sinai Health SystemDirector, Regulatory & Administrative Affairs - Institute for Transformative Clinical TrialsNew York, NY$95,450–$143,175 / yearThe Director of Regulatory & Administrative Affairs for the Mount Sinai Institute for Transformative Clinical Trials provides strategic leadership and operational oversight for regulatory, safety, and administrative activities supporting a portfolio of sponsor-led, investigator-initiated, federally funded, and industry-sponsored clinical research studies. Mount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time - discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it.
Staff Regulatory Affairs Specialist Becton Dickinson and CoStaff Regulatory Affairs SpecialistFranklin Lakes, NJ$135,500–$216,800 / yearFor most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Senior Manager, Regulatory Affairs US Advertising And Promotion - Immunology - Hybrid AbbVie, IncSenior Manager, Regulatory Affairs US Advertising And Promotion - Immunology - HybridFlorham Park, NJApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. The Senior Manager Regulatory Affairs US Advertising and Promotion-Immunology combines knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet the required legislation.
Senior Manager Regulatory Affairs US Advertising and Promotion - Immunology - Hybrid AbbVie IncSenior Manager Regulatory Affairs US Advertising and Promotion - Immunology - HybridFlorham Park, NJApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
NewSr Manager, International Device Regulatory Affairs Biogen IncSr Manager, International Device Regulatory AffairsNY$138,000–$184,500 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. About This Role: As the Senior Manager of International Device Regulatory Affairs, you will lead regulatory strategies and execution for high-risk implantable medical device submissions beyond the United States, focusing on Japan, China, and Latin America.
Director US Advertising and Promotion Global Regulatory Affairs SanofiDirector US Advertising and Promotion Global Regulatory AffairsMorristown, NJ$178,500–$257,833.33 / yearThe Director is responsible for decision-making, direction, and oversight of the day-to-day activities of their assigned products, departmental activities, and direct reports (if applicable) in order to meet internal and external customer needs. About the job: As the Director, US Advertising and Promotion, Global Regulatory Affairs within our GRA Advertising and Promo Team, you will be responsible for decisions, providing strategic direction and oversight for the day-to-day activities for assigned products.
Director US Advertising And Promotion Global Regulatory Affairs SanofiDirector US Advertising And Promotion Global Regulatory AffairsMorristown, NJ$178,500–$257,833.33 / yearThe Director is responsible for decision-making, direction, and oversight of the day-to-day activities of their assigned products, departmental activities, and direct reports (if applicable) in order to meet internal and external customer needs. About the job: As the Director, US Advertising and Promotion, Global Regulatory Affairs within our GRA Advertising and Promo Team, you will be responsible for decisions, providing strategic direction and oversight for the day-to-day activities for assigned products.
Associate Director, Global Regulatory Affairs EisaiAssociate Director, Global Regulatory AffairsNutley, New JerseyE-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Skills:Communication & Cross-functional Influence, Critical Thinking & Business Agility, Mentoring/ People Development, Project Management, Regulatory Strategy Acumen Eisai Salary Transparency Language:
Associate Director, Global Regulatory Affairs Eisai IncAssociate Director, Global Regulatory AffairsNutley, NJE-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Responsibilities: Lead the drafting, compilation of routine (and support complex) submissions of documents (e.g., meeting requests, iPSPs/PIPs, protocol amendments) to health authorities.
NewDirector Research Regulatory Affairs Rutgers The State University of New JerseyDirector Research Regulatory AffairsNew Brunswick, NJUnder Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption. Among the key duties of the position are the following: Provides strategic leadership and oversight for the university's comprehensive research compliance and security programs, reporting to the Assistant Vice President for Research Regulatory Affairs.
NewSenior Manager Regulatory Affairs Advertising and Promotion SanofiSenior Manager Regulatory Affairs Advertising and PromotionMorristown, NJ$122,250–$176,583.33 / yearAs the Senior Manager, Regulatory Affairs Advertising and Promotion within our GRA Advertising and Promo Team, you will be responsible for conducting the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns. With some direction from the Therapeutic Area Head, will conduct the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns, including serving as regulatory lead for product launches.
NewSenior Manager Regulatory Affairs Advertising And Promotion SanofiSenior Manager Regulatory Affairs Advertising And PromotionMorristown, NJ$122,250–$176,583.33 / yearAs the Senior Manager, Regulatory Affairs Advertising and Promotion within our GRA Advertising and Promo Team, you will be responsible for conducting the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns. With some direction from the Therapeutic Area Head, will conduct the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns, including serving as regulatory lead for product launches.
NewRegulatory Affairs Director *PC 954 Miltenyi Biotec GmbHRegulatory Affairs Director *PC 954New Jersey, NJ$201,579–$237,206 / yearThese developments have led to cutting-edge cell and gene therapies - transformative methods that mobilize the body's own cells and genetic blueprint to tackle diseases such as cancer and autoimmune conditions. Essential Duties and Responsibilities: Develop and implement CMC regulatory strategies to support clinical development, marketing applications, and post-approval lifecycle management for cell and gene therapy products.
Senior Regulatory Affairs Specialist Ouraring IncSenior Regulatory Affairs SpecialistNY$151,300–$178,000 / yearThe ideal candidate brings hands-on experience in medical device or digital health regulatory affairs, strong operational discipline, and the ability to work cross-functionally with quality, engineering, product, clinical, and legal teams in a fast-paced environment. This role will help drive compliant and efficient execution of regulatory activities across the product lifecycle, including submission support, document management, change assessments, registrations, regulatory intelligence, and inspection/audit readiness.
Senior Director, Global Regulatory Affairs, Neurology Eisai USSenior Director, Global Regulatory Affairs, NeurologyNutley, NJResponsibilities: Function as a Regional or Global Regulatory strategy lead and oversee regulatory submission activities and review regulatory documents (e.g., annual reports, protocol amendments) prior to submission to ensure overall quality, compliance and timelines. Direct, and manage financial planning/forecasting and budget management, vendor management, timeline development & tracking, and assess resource needs for respective program(s) within regulatory strategy.
Regulatory Affairs Director IQVIA Holdings IncRegulatory Affairs DirectorParsippany, NJ$103,600–$288,600 / yearPossesses a specific regulatory or technical expertise; Good, solid interpersonal communication (oral and written) and organization skills; Strong software and computer skills, including Microsoft Office applications; Demonstrates negotiation skills and is confident in making decisions with minimal supervision; Ability to work on several projects, retaining quality and timelines; Possess demonstrated working knowledge of corresponding professional grade level responsibilities, skills and abilities, as required for guidance of staff. Possess practical knowledge in leading and managing the execution of processes, projects and tactics within one department or multiple related departments; Ability to exercise independent judgement taking calculated risks when making decisions; Applicable certifications and licenses as required by country, state, and/or other regulatory bodies.
Quality - Regulatory Affairs Manager Englewood Lab, Inc.Quality - Regulatory Affairs ManagerTotowa, NJFull timeThe position serves as the primary regulatory lead for operational execution at the site and ensures effective communication between site operations and global quality leadership. Conduct regulatory reviews of formulas and ingredients to ensure compliance across all intended markets; proactively identify regulatory risks and implement mitigation plans.
Regulatory Affairs Manager Actalent IncRegulatory Affairs ManagerNJ$90,000–$115,000 / yearOversee the preparation, review, and maintenance of regulatory documents, including TDS, SDS, allergen and GMO statements, nutritional and natural certifications, Non-GMO Project forms, Kosher and Halal certifications, certificates of origin (COO), Prop 65 documentation, flavor labeling, TTB submissions, and related materials. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC-with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Head of Regulatory Affairs Revolut LtdHead of Regulatory AffairsNY$207,000–$217,900 / yearThey stay ahead of regulatory change, provide timely responses to enquiries, and work across the business to ensure compliance is always in step with innovation. People who love building great products, redefining success, and turning the complexity of a chaotic world into the simplicity of a beautiful solution.
2027 Future Talent Program - Global Regulatory Affairs & Compliance US Subsidiary - Intern Merck & Co Inc2027 Future Talent Program - Global Regulatory Affairs & Compliance US Subsidiary - InternRahway, NJAs a Summer Intern, you will have the opportunity to gain hands-on experience in pharmaceutical regulatory affairs by supporting the Drug Shortages & Support Functions team and various company and industry-wide initiatives through cross-functional collaboration with internal and external stakeholders. The team partners with stakeholders across Regulatory Affairs, Manufacturing, Supply Chain, Quality, Medical Affairs, Communications, and Legal to help prevent, mitigate, and minimize the impact of supply disruptions on patients, while ensuring compliance with applicable regulatory requirements.