Hybrid Senior Regulatory Affairs Program Lead – Data Strategy, MedTech Surgery

Posted 2 hours ago

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About the role

  • Senior Regulatory Affairs Program Lead managing data strategy for Johnson & Johnson's Surgery group. Supporting regulatory processes and data strategies in hybrid work environment.

Responsibilities

  • Translate complex regulatory requirements into clear, practical implementation strategies, ensuring that regulations are reflected accurately and efficiently within business processes, and supporting digital systems.
  • Lead regulatory strategy and implementation for AI-driven digital and data initiatives, ensuring development of validated, compliant processes and tools to collect, manage, and analyze data that strengthen our competitive position and meet evolving external data- and systems-related regulatory requirements.
  • Establish and optimize procedures governing the creation, maintenance, and utilization of regulatory data to ensure integrity, traceability, and compliance.
  • Build organizational capabilities in regulatory data standards, processes, and systems.
  • Serve as the primary contact for enterprise-wide initiatives, influence, and drive alignment with interested parties.
  • Translate Regulatory Affairs’ needs into actionable business requirements to guide the design, development, and deployment of IT solutions, digital tools, and data platforms.
  • Support policy efforts by providing input on emerging regulations, industry guidance, and trade association activities.
  • Lead organizational readiness for data submissions to external databases (e.g., EUDAMED) including defining data requirements, conducting gap analysis, and ensuring process and system preparedness.

Requirements

  • Minimum of a Bachelor’s Degree required , Advanced Degree strongly preferred .
  • At least 6+ years regulatory affairs experience within a highly regulated industry required , Medical Device strongly preferred .
  • Compliance & governance for Unique Device Identification (UDI) is required .
  • System implementation experience is required .
  • Experience implementing AI into processes & workflows is highly desired .
  • Knowledge of regulatory requirements in the EU and US, with proven track record of translating regulatory requirements into clear data, system, and business processes.
  • Excellent written and verbal communication skills.
  • RAC Certification strongly preferred .

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)).
  • 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 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

Job title

Senior Regulatory Affairs Program Lead – Data Strategy, MedTech Surgery

Job type

Experience level

Senior

Salary

$109,000 - $174,800 per year

Degree requirement

Bachelor's Degree

Location requirements

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