Manager, Regional Regulatory Affairs - Cross-Regional Operations and Strategy Support

About this role

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, Titusville, New Jersey, 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 https://www.jnj.com/innovative-medicine

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with 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): • United States - Requisition Number: R-086945

• Brazil - Requisition Number: R-088587

• Poland - Requisition Number: R-088589

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Johnson & Johnson Innovative Medicine R&D is recruiting for Manager, Regional Regulatory Affairs - Cross-Regional Operations and Strategy Support (C-ROSS).  This position is a hybrid role and can be located in Raritan, NJ; Titusville, NJ; or Spring House, PA.

The Manager, Regional Regulatory Affairs - C-ROSS will reside within Global Regulatory Affairs and provide regional regulatory strategic implementation support for products in one or more therapeutic areas (TAs).  This individual will be responsible for collaborating with the Global and Regional Regulatory Leaders, functional area experts and Local Operating Companies to implement/execute the company’s regulatory strategies for both marketed products and products under development in line with R&D, regional and local business objectives.  This individual will function in a matrix environment and must exhibit strong leadership skills.

Principal Responsibilities: • Implementation of the regional regulatory strategy, including the regulatory submission plans, in line with R&D, regional and local business objectives.

• Represent the regions and contribute to the regional and global regulatory strategy through participation in product-related teams such as, Global Regulatory Teams, submission teams, Labeling Working Groups, Clinical Trial Application (CTA) Working Groups, response teams, clinical teams, etc., and provide team leadership where appropriate.

• Advise product teams regarding regional and local requirements and impact of supply chain decisions on regional registrations to efficiently implement regional regulatory strategies.

• Lead the Regional Working groups to ensure timely execution of product objectives and align regional deliverables with those of the global teams.

• Facilitate tactical implementation at the regional level and ensure ongoing and effective communications with the regional and global teams on product activities and issues.

• Leverage TA, strategic, tactical, operational, and procedural synergies and efficiencies across regions.

• Provide regulatory input for and appropriate follow-up to inspections, audits, litigation support and product complaints.

• Liaise directly with Local operating companies as needed and apply the understanding of worldwide health authorities and applicability of procedures to the regions to help in the preparation for meetings with regulatory agencies in the regions.

• Oversee management of responses to questions asked by Health Authorities in a timely manner and in line with the product strategy.

• Development of regional marketing approval submission plans in collaboration with Regional and Global regulatory teams, development of tactical planning and timelines, including submission plans, review and preparation submission documents for the products’ life cycle, and communication to relevant groups.

• Preparation of registration dossiers (e.g., International Common Technical Document (iCTD) and ASEAN Common Technical Document (ACTD)) and dossier re-use strategies.

• Manage and track country-specific requirements for local submission purposes (e.g.  legal and technical documents, RMP).

• Oversee development of labeling negotiation strategies for countries in the regions and development of supporting documentation for labeling.

• Be current with using Gen AI tools, such as co-pilot.

Qualifications: • A minimum of a Bachelor’s degree in a scientific or technical discipline is required.  Advanced degree (Master’s, PharmD, Ph.D.) in a scientific or technical discipline preferred.

• A minimum of 6 years of relevant regulatory experience (3 years in pharmaceutical regulatory) with a Bachelor’s degree; a minimum of 4 years of relevant regulatory experience (2 years in pharmaceutical regulatory) with a Master’s or PharmD degree; or a minimum of 2 years of relevant regu

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