Director, Enterprise Regulatory Compliance

Johnson & Johnson Innovative Medicine•Horsham, PA

4d•$150,000 - $258,750•Hybrid

About The Position

Johnson & Johnson is currently seeking a Director, Enterprise Regulatory Compliance, to join our Enterprise Regulatory Compliance Assessment team, located in New Brunswick, Raritan, Titusville, NJ and Horsham, PA. The Director, Enterprise Regulatory Compliance reports to the Senior Director, Head of Assessment, Enterprise Regulatory Compliance, and serves as an enterprise point of contact for cGMP regulatory compliance matters across Medical Devices and Pharmaceuticals. This role provides independent oversight of compliance risks and trends, partners with Quality and Compliance, and Regulatory Intelligence leaders to identify and mitigate emerging risks and delivers clear insights to senior leadership to support sound, risk-based decisions.

Requirements

A minimum of a bachelor’s degree is required.
A minimum of 10 years’ relevant quality and compliance experience is required.
Prior work experience in cGMP regulatory compliance in medical device and/or pharmaceutical regulations is required.
Strong written and oral communication skills that can be adapted to the appropriate levels of a large complex organization to facilitate regulatory compliance risk understanding is required.
Track record of successful leadership skills in cGMP compliance is required.
Ability to build productive relationships to work and influence effectively across cultures and functions without line authority is required.
Ability to work with and effectively influence all levels within the organization is required.
Self-direction and ability to thrive in a complex matrixed environment is required.

Nice To Haves

Advanced degree in an applicable field of study or certification is preferred.
Work experience for a Health Authority or Notified Body is preferred but not required.

Responsibilities

Serve as the Enterprise Regulatory Compliance Single Point of Contact and subject-matter leader for policy interpretation, issue triage, and decision support across pharmaceutical and medical device businesses.
Provide independent assessments of manufacturing, quality, and compliance risks, supporting consistent application of global regulations, company standards, and policies across segments and sites.
Independently review and classify Health Authority inspections and corporate cGMP audits to ensure consistency across businesses.
Independently review and initiate issue management for health authority inspections and recalls across the pharmaceutical and medical device businesses following escalation policies and standards.
Support inspection readiness activities in preparation for Health Authority and Notified Body audits and pre-approvals.
Review US FDA response reviews, as assigned, to ensure completeness, quality, and alignment with applicable requirements.
Analyze large volumes of regulatory compliance data to identify actionable insights and lead periodic data driven compliance reviews for senior executive leadership.
Actively build and maintain AI literacy and fluency, and apply approved AI enabled tools to improve individual and team ways of working (e.g., analysis, synthesis, documentation, and quality checks), in alignment with data governance, privacy, and responsible AI expectations.
Lead enterprise interpretation, oversight, and governance for significant compliance escalations, including alignment on required actions and communications to senior leadership.
Participate, as needed, in corporate regulatory compliance audits, due diligence, and acquisition compliance assessments; develop strategic plans aligned with enterprise objectives and influence outcomes in a complex, matrixed organization.
Provide consultative expertise on compliance issue management, including support for health authority responses and field action decisions in accordance with policy requirements.
Provide cGMP training to corporate and internal audit teams on risk-based auditing strategies for key compliance issues and emerging trends.

Benefits

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.
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 period10 days
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year