Sr. Regulatory Affairs Professional

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an 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:Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of AmericaJob Description:About Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.Learn more at are searching for the best talent for a Sr. Regulatory Affairs Professional, located in Spring House, PA, Raritan or Titusville, NJ.This position is strictly suited for candidates with early professional experience who are looking to develop their careers in regulatory affairs.Global Regulatory Affairs (GRA) is looking for a high energy, inventive, self-starter who is passionate about advancing their career in healthcare. GRA is a key strategic partner supporting global R&D initiatives at Johnson & Johnson Innovative Medicine. As a Sr. Regulatory Affairs Professional you will support drug development programs as well as marketed products across multiple therapeutic areas. You will gain broad and diverse regulatory experience supporting compounds in early to late drug development as well as life-cycle activities for approved products in our portfolio via a flexible rotational model geared towards addressing business needs and individual career-development goals.Through hands-on, real-world experiences, you will work on projects that improve your leadership, problem solving, and creative thinking skills. Furthermore, you will acquire the business savvy to be successful in a complex, fast-paced, and innovative regulatory environment.You will be responsible for:Participate in global and regional regulatory team meetings and advise the regulatory team on applicable regulatory requirements, project-specific regulatory issues as assignedDevelop an understanding of the regional regulatory environment, competitor intelligence, and therapeutic areaAssist in the preparation of meetings and act as backup for contact with Regulatory Agencies as neededEnsure responses to Regulatory Agency queries are made in a timely manner, and that content is consistent with the regulatory strategyWork cross-functionally, interact with internal and external colleagues with coordination between departments, and lead team meetings as appropriateAdvise team in required documents and submission strategiesReview clinical trial plans, protocols and submission plans ensuring alignment with regulatory requirementsSupport the development and improvement of processes related to regulatory submissionsProvide regulatory input for and follow-up to inspections, audits, litigation support, and product complaintsStay on top of current and pending approvals in assigned therapeutic areas and is knowledgeable of laws, guidelines and requirements related to those areasMay interact with Health Authorities (HA) regarding program-specific issues and serve as secondary HA point-of-contact to represent J&J/Janssen externally with some degree of supervisionQualifications / Requirements:Education:Pharm D/PhD with 2-5 years’ experience OR Masters with 3-5 years of experience is required. This position is strictly suited for candidates with early professional experience who are looking to develop their careers in regulatory affairs.Experience and Skills Required: Understanding of the drug development process.Preferred:Previous experience in a health regulated industryUnderstanding of regulatory submission and approval process and applicable US and EMA regulatory guidelinesRelevant regulatory affairs experience in pharmaceutical/biotechExperience responding to HA requests, managing HA interactions, and life cycle management applicationsDiverse therapeutic area experienceExperience within a cross-functional team environment as an individual contributor and decision makerProactively anticipates issues; exercises judgment in developing new approaches/solutions and resolving issuesInfluences or persuades others within area of immediate responsibility, scope, and level to accept new ideas, practices and approachesSkilled at project managing and effectively prioritizing assignments for multiple projects simultaneouslyStrong interpersonal and communication skills#LI-HybridThe expected base pay range for this position is $109,000- $174,800.The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis. Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits:Vacation –120 hours per calendar yearSick time - 40 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar yearHoliday pay, including Floating Holidays –13 days per calendar yearWork, Personal and Family Time - up to 40 hours per calendar yearParental Leave – 480 hours within one year of the birth/adoption/foster care of a childCondolence Leave – 30 days for an immediate family member: 5 days for an extended family memberCaregiver Leave – 10 daysVolunteer Leave – 4 daysMilitary Spouse Time-Off – 80 hours Additional information can be found through the link below. For additional general information on Company benefits, please go to: The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. This job posting is anticipated to close on 5/21/2026. The Company may, however, extend this time-period, in which case the posting will remain available on to accept additional applications.Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via , internal employees contact AskGS to be directed to your accommodation resource.Required Skills: Preferred Skills:Analytical Reasoning, Business Writing, Coaching, Collaborating, Communication, Legal Support, Problem Solving, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Regulatory Reporting, Risk Assessments, Strategic ThinkingSummaryLocation: Raritan, New Jersey, United States of America; Titusville, New Jersey, United States of America; Spring House, Pennsylvania, United States of AmericaType: Full time