Director, Regulatory Affairs
Johnson & Johnson Innovative Medicine
Johnson & Johnson Innovative Medicine R&D is seeking a Senior Manager, North America Regulatory Liaison. This hybrid role will be located in Spring House, PA; Titusville, NJ; or Raritan, NJ. You will lead NA regulatory strategy and execution for Immunology projects, partnering with global teams to shape development pathways and ensure timely Health Authority interactions. You will drive end-to-end planning, submission deliverables, and lifecycle management, influencing decisions across a #J-18808-Ljbffr
$137k - $235.75k
...dignity of our employees and recognize their merit.Job Function: Regulatory Affairs GroupJob Sub Function: Regulatory AffairsJob Category:... ...more at We are searching for the best talent for an Associate Director, Regulatory Affairs, North American Regional Leader (NARL)...SuggestedFull timeLocal areaImmediate startFlexible hours$137k - $235.75k
...dignity of our employees and recognize their merit.Job Function: Regulatory Affairs GroupJob Sub Function: Regulatory AffairsJob Category:... ...Johnson Innovative Medicine R&D is recruiting for an Associate Director, Regulatory Affairs Labeling Product Leader. This position...SuggestedFull timeWork experience placementLocal areaImmediate startWorldwide$164k
..., for each other, and for the future of science, we're in. Are you? About the Role: We're looking for an Associate Director, Regulatory Affairs CMC on the Regulatory Affairs CMC team to help us expand what's possible for patients with serious diseases. Reporting to...SuggestedTemporary workLocal areaRemote workFlexible hours$137.6k - $180k
...that promotes professional growth and a significant impact on patients' lives. Reporting Structure Reports To: Director, Regulatory Affairs - Advertising, Promotion, and Labeling Direct Report(s): None Areas Managed: Advertising & Promotion North America...SuggestedTemporary workNight shiftWeekend work- ...change but actively creates it—where your skills and values drive our collective progress and impact.The Senior Director of Advertising & Promotion- Regulatory Affairs drug and device products manages and, if required participates in, the reviews and approvals of advertising...SuggestedTemporary workWork at officeFlexible hours
$193.04k - $289.56k
...for patients, their families, and society.Job SummaryThe Global Regulatory Lead (GRL) is responsible for leading and developing global... ...interactions. The GRL is responsible for representing Global Regulatory Affairs on the Global Project Team (GPT), as well as in early- and...$166.72k - $250.08k
...", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary The Associate Director, Regulatory Affairs Advertising and Promotion (RAAP) provides strategic and tactical regulatory support for U.S. promotional and selected non...Work at office- ...Director, Compliance Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with capabilities in product... ...as the standing Compliance member of the Medical, Legal, and Regulatory review committee; ensure promotional and non-promotional...Contract workFor contractorsFixed term contract
- ...Regulatory Affairs Manager Job DescriptionManage Company's Regulatory Affairs for assigned products for US and Canada, including implementation of the overall regulatory strategy, preparation of regulatory submissions and interface with relevant health authorities.Implement...
$160k - $180k
...team success. We have an opening in our Monmouth Junction, NJ office for an experienced Associate Director or Director, Advertising & Promotions to join our Regulatory Affairs team. Title and salary commensurate with experience. This position provides senior regulatory...Full timeWork at office- Daiichi Sankyo, Inc. seeks an Associate Director, Regulatory Affairs Advertising and Promotion to provide regulatory review and strategic guidance for U.S. promotional and some non-promotional communications across its portfolio. Reporting to the Head of RAAP, this role...
- ...financial flexibility by offering contingent labor as a variable cost.Job DescriptionThis individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan annual...Work at officeImmediate start
- ...both internal and external cross-functional project teams.• The Regulatory CMC Technical Associate may be called upon to author technical... ...Master s Degree a plus• 4+ years of pharmaceutical regulatory affairs experience• Strong knowledge of NDA, ANDA, MAA, BLA, CTA, or...Work at officeLocal areaImmediate start
- ...individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.Job Function: Regulatory Affairs GroupJob Sub Function: Regulatory AffairsJob Category:ProfessionalAll Job Posting Locations:Cincinnati, Ohio, United States...Full timeLocal areaImmediate startRemote work
$168.37k - $220.99k
...capabilities to advance innovative immunotherapies for patients living with multiple myeloma. Legend Biotech is seeking a Director, Regulatory Affairs as part of the Regulatory Affairs team based in Somerset, NJ. Role Overview The Director of Regulatory...Permanent employmentFull timeTemporary workFor contractorsLocal areaWorldwideFlexible hours- ...to join a dynamic and growing team with established products and an entrepreneurial mindset. Role Description: The Director, Regulatory Affairs is responsible for leading and executing regulatory activities to support global product registrations and lifecycle...Worldwide
$190k - $230k
Description:This position serves as a multifaceted leadership role within the Compliance function, overseeing a diverse portfolio of responsibilities. The successful candidate will lead key operational aspects of Amneal's Compliance program, including managing our global...Temporary workLocal areaFlexible hours- ...Regulatory Affairs AssociateAs a Regulatory Affairs Associate you will:Gain experience and exposure to groundbreaking programs and strategies for compounds in development and/or marketing products intended to address unmet medical needs in markets globally. Learn the...
- Tris Pharma, Inc. is seeking an Associate Director or Director in Regulatory Affairs Advertising & Promotions for a hybrid role in Monmouth Junction, NJ. The position offers senior regulatory oversight over promotional materials to ensure FDA compliance and alignment with...
- ...join a dynamic and growing team with established products and an entrepreneurial mindset. Role Description: dThe Regulatory Affairs (RA) Specialist is responsible for supporting global regulatory submissions and compliance activities to ensure medical device...InternshipWork at officeWorldwide
$94k - $151.8k
...System Lead, is responsible for establishing and maintaining a robust compliance program to ensure compliance with all applicable regulatory requirements, company policies and procedures, and J&J Corporate requirements. The Staff Source Compliance Specialist will...Full timeTemporary workWork experience placementLocal areaImmediate start$28.5 - $35 per hour
...compliance with state and federal regulations. Responsibilities include oversight of sample collection, development and review of regulatory reports, and assistance in the implementation of new environmental compliance initiatives. The ideal candidate should have...Hourly payFull timeTemporary workWork at officeLocal area$93k - $172.9k
...Automation). The Opportunity Assist in activities associated with regulatory approval of in vitro diagnostic medical devices in global... ...subject. 5 years of experience in regulatory, development, clinical affairs, quality, or program management in IVD, medical device, or...Local areaRemote workRelocation package- Johnson & Johnson Innovative Medicine is seeking a Senior Manager, Regulatory Affairs Labeling Product Leader for a hybrid role based in New Jersey or Pennsylvania. You will drive global labeling strategy, lead target labeling development, and collaborate with cross-functional...
- Medasource is seeking a Regulatory Program Manager to lead global regulatory strategies and execution for oncology programs. The role requires coordinating cross-functional teams, managing submissions, and accelerating timelines. Expect a high-visibility, hybrid work arrangement...
- ...create.Location: Westchester, IL/Bridgewater, NJWorkplace type: Hybrid- 3 days/week on-site & 2 day/week remoteIngredion is seeking a Director, Corporate Strategy that will facilitate and support strategy and growth activation at Corporate, Segment, and Functional levels...Full timeWork at officeRemote workWorldwideRelocation2 days per week3 days per week
$164k - $282.9k
...recognize their merit.Job Function: Medical Affairs GroupJob Sub Function: Medical... ...are searching for the best talent for the Director, Global Medical Affairs Strategy & Execution... ...global and regional marketing directors, regulatory leaders, outcomes research and...Full timeLocal areaImmediate startWorldwide$18 - $20 per hour
Credentialing and Provider Enrollment Specialist Job Category : Human Resources Requisition Number : CREDE003404 Posted : August 3, 2026 Full-Time On-site Locations Showing 1 location Pay or shift range: $18 USD to $20 USD The estimated range is the budgeted amount for ...Full timeShift work$178k - $307.05k
...AmericaJob Description:DePuy Synthes is recruiting for a Sr. Director, Regulatory Law, located in Raynham, MA, New Brunswick, New Jersey, West... ...regulatory matters, partners closely with Regulatory Affairs, Quality, R&D, and Commercial teams, and helps shape regulatory...Full timeImmediate start$25 - $30 per hour
Job Description Job Description We are looking for a Crew Chief for an immediate hire opportunity in Bridgewater, NJ! A well established water damage restoration company is seeking an experienced Crew Chief/Water Restoration Tech. If you are looking to continue your...Live inLocal areaImmediate startMonday to Friday
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