Senior Manager, North America Regulatory Liaison

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 innovate across the full spectrum of healthcare solutions to deliver breakthroughs that profoundly impact health for humanity.

About the role

Johnson & Johnson Innovative Medicine R&D is recruiting for a Senior Manager, North America Regulatory Liaison. This hybrid role will be located in Spring House, PA; Titusville, NJ; or Raritan, NJ. The Senior Manager will serve as a strategic regulatory leader, driving North America regulatory strategy and execution for assigned Immunology projects. This role partners closely with global and cross-functional leaders to shape development pathways, influence key decisions, and ensure high-quality, timely interactions with Health Authorities. The position requires a strategic mindset, balancing risk mitigation with opportunity maximization to enable successful Immunology product development and lifecycle management.

Responsibilities

• Regulatory Strategy & Leadership:
  • Contribute to and help shape regulatory submission strategies, identifying risks, mitigation plans, and opportunities.
  • Provide strategic regulatory input into key development documents (e.g., clinical protocols, study reports, summaries).
  • Apply knowledge of regional and global regulatory frameworks, trends, and requirements across all phases of development.
• Submission Planning & Execution:
  • Lead the planning, preparation, and delivery of regulatory submissions (simple to complex) across the product lifecycle.
  • Develop and maintain submission delivery timelines, content plans, and execution strategies.
  • Author and/or critically review submission components, ensuring quality and compliance.
  • Manage regulatory applications and associated procedures through Health Authority approvals.
• Health Authority Engagement:
  • Serve as primary point of contact with Health Authorities (e.g., FDA).
  • Lead and coordinate Health Authority interactions, including preparation of briefing materials and responses.
  • Manage responses to regulatory queries and requests.
• Cross-functional Collaboration:
  • Partner with global regulatory and cross-functional teams to align on submission and interaction plans.
  • Lead or contribute to cross-functional submission teams to ensure timely and effective execution.
  • Communicate clear, proactive status updates to stakeholders.
• Operational Excellence & Influence:
  • Identify and drive process improvements, applying critical thinking and problem-solving skills.
  • Demonstrate strategic thinking, including contingency planning aligned with business objectives.
  • Influence decision-making across a matrixed organization.
• Representation & Networking:
  • Represent the company externally with Health Authorities and industry partners, as appropriate.
  • Build and leverage strategic relationships and networks.
• Additional Scope:
  • May serve as Regional Regulatory Leader for assigned programs.

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 8 years of relevant regulatory experience with a Bachelor’s degree; a minimum of 6 years with a Master’s or PharmD degree; or a minimum of 4 years with a Ph.D. is required.
• Experience in pharmaceutical, biotech, or OTC industry is required.
• Strong knowledge of clinical drug development and regulatory pathways is required.
• Experience managing lifecycle submissions (e.g., IND, NDA, CTA, MAA) is required.
• Demonstrated experience preparing, reviewing, and delivering regulatory documentation is required.
• Proven track record interacting with FDA and other global Health Authorities is required.
• Experience in Immunology therapeutic area preferred.
• Experience in people management/coaching/mentoring is preferred.
• Excellent communication and interpersonal skills.
• Strong stakeholder management skills.
• Ability to exercise independent judgment in resolving complex regulatory and organizational challenges.
• Strong leadership capabilities with the ability to work successfully in a matrixed environment.
• Ability to effectively prioritize assignments for multiple products and projects simultaneously.
• Ability to collaborate with all levels and influence decision-making within a cross-functional organization.
• This position may require up to 10% travel.

Pay

The anticipated base pay range for this position is $137,000.00 - $235,750.00.

Benefits

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: (Subject to the terms of their respective policies and date of hire)
  • Vacation – 120 hours per calendar year
  • Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado – 48 hours per calendar year; for employees who reside in the State of Washington – 56 hours per calendar year
  • 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 go to: https://www.careers.jnj.com/employee-benefits.