Mgr Global Regulatory Scientist, Reg Aff

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 Group Job Sub Function Regulatory Affairs Job Category Professional All Job Posting Locations Raritan, New Jersey, United States of America; Spring House, Pennsylvania, United States of America Job Description About Innovative Medicine: Our 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 . We are searching for the best talent for a Manager Global Regulatory Scientist, Regulatory Affairs. This hybrid work position will be in Beerse, Belgium; Leiden, Netherlands; High Wycombe/Maidenhead, UK; or Raritan, NJ and Spring House, PA (USA). Key Responsibilities Draft cover letters and support the preparation of various applications (e.g., IND, CTA, MAA/NDA and eCTD), and procedures for Regulatory Agency submissions. For CTA/INDs – ensure protocols are in alignment with regulatory requirements and provide advice on required documents and submission strategies in preparation for those filings. For Marketing Authorization Applications (NDA, MAA or other major HA submissions): provide regulatory support throughout the registration process. Advise team on required documents and submission strategies in preparation of NDA, MAA (and other global filings) as assigned in collaboration with LOCs as appropriate. Assist with timely NDA, MAA (other) availability, ensure that all document components are in place on time, identify and track critical path activities. Assist with submission and acceptance of Marketing Authorization Applications (NDA, MAA, other). Ensure country-specific submission packages are made available to the LOCs in accordance with agreed plans. Assist in the preparation of meetings with Regulatory Agencies. Coordinate, contribute to development, and review the content of responses to queries from HAs to ensure high quality and timely responses. May include other activities as delegated by the RRL/GRL. Liaise with LOCs, track dates of submissions/responses to queries in a timely manner. Acts as back up contact/representative on specific multi-discipline teams, or with regulatory agencies as needed. May be responsible for organizing and leading meetings. Provide regulatory input for and appropriate follow‑up to inspections, audits, litigation support, and product complaints. Supports GRL(GRT) by driving high project management planning of global submissions or health authority interactions and additional major regulatory milestones. Participate in global regulatory team meetings as appropriate. Assist in strategy development by researching regulatory and medical information in preparing submissions to global health authorities (HAs). Advise the regulatory team on applicable regulatory requirements, project-specific regulatory issues as assigned. Partner with regulatory colleagues to understand the competitive landscape, e.g., views of HAs, regulatory precedents, labeling differences, and disease-area specific issues. May assist in the development and improvement of regulatory processes. Qualifications, Experience and Skills A bachelor's degree in a scientific or equivalent discipline; an advanced scientific degree is preferred, and at least 6 years of health-regulated industry experience, or a master’s degree and a minimum of 5 years of health-regulated industry experience, or a PhD/PharmD with a minimum of 4 years of health-regulated experience. At least 4 years of relevant regulatory affairs experience in the pharmaceutical/biotech industry is required. Opportunity to flex across different product types (pharma, devices, combo products). Knowledge of multiple global health authorities' regulations and processes would be ideal. Solid understanding of FDA and ICH regulatory requirements and guidelines specific to the areas of clinical research, product development, lifecycle submission management and product labeling is required. Therapeutic area experience in oncology is beneficial. Experience with combination products (drug and devices) would be an asset. Intellectual curiosity and an ability/flexibility in learning new things and working in novel areas with limited regulatory precedence. Experience preparing responses to health authorities, managing health-authority interactions, and lifecycle management of clinical trials and marketing authorization submissions (e.g., IND/CTAS/NDA/BLA, MAAS). Experience in strategic planning, technical data summary and cross-functional management is required. Leadership Capabilities Strong organizational and time management skills. Strong collaboration skills, including effective communication and conflict resolution skills. Strong leadership capabilities and ability to work successfully in a matrixed environment. Effective critical thinking, including problem solving and goal setting. Demonstrated ability to think strategically and contingency plan in order to meet business objectives. 10% domestic travel and potential international travel may be required for this position. Please note that this role is available across multiple countries and may be posted under different requisition numbers to follow local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s). Belgium, Netherlands – Requisition Number: R-088321 United Kingdom – Requisition Number: R-089114 Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission. Required Skills Analytical Reasoning, Business Writing, Coaching, Compliance Risk, Fact-Based Decision Making, Industry Analysis, Legal Support, Process Improvements, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Risk Assessments, Strategic Thinking, Technical Credibility. Preferred Skills Analytical Reasoning, Business Writing, Coaching, Compliance Risk, Fact-Based Decision Making, Industry Analysis, Legal Support, Process Improvements, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Risk Assessments, Strategic Thinking, Technical Credibility. Compensation The anticipated base pay range for this position is: $117,000.00 – $201,250.00. Benefits and Pay Transparency 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)). This position is eligible to participate in the company’s long-term incentive program. Time off benefits: Vacation – 120 hours per calendar year; Sick time – 40 hours per calendar year (48 hours for Colorado residents, 56 hours for Washington residents); Holiday pay, including floating holidays – 13 days per calendar year; Work, personal and family time – up to 40 hours per calendar year; Parental leave – 480 hours within one year of the birth/adoption/foster care of a child; Bereavement leave – 240 hours for an immediate family member, 40 hours for an extended family member per calendar year; Caregiver leave – 80 hours in a 52-week rolling period; Volunteer leave – 32 hours per calendar year; Military spouse time‑off – 80 hours per calendar year. For additional general information on company benefits, please visit: . #J-18808-Ljbffr Johnson & Johnson Innovative Medicine