The Sr. Source Regulatory Compliance Specialistis responsible forexecuting and supporting regulatory compliance activities related to sourcing, suppliers, and externally provided processes. This role ensures that suppliers, contract manufacturers, and sourced materialscomply withapplicable regulatory requirements, quality system standards, and internal policies. The position plays a key role in safeguarding product quality, supporting audit readiness, and enabling compliant supply continuity by partnering closely with Quality, Regulatory Affairs, Supply Chain, and Procurement teams across EMEA.

Key Responsibilities

• Execute sourceregulatory compliance activities to ensure adherence to regulatory and quality system requirements.

• Support compliance oversight for suppliers, contract manufacturers, and externally provided processes.

• Partner with Supply Chain, Procurement, Quality, and Regulatory Affairs teams to support compliant supplier qualification and lifecycle management.

• Interpret regulatory requirements and support translation into sourcing and supplier compliance expectations.

• Support internal audits, external audits, and health authority inspections related to sourcing and supplier compliance.

• Monitor compliance risks, trends, and supplier performancemetrics;support corrective and preventive actions.

• Ensureaccuratemaintenance of compliance documentation, records, and reports.

• Contribute to continuous improvement initiatives to strengthen sourcingcompliancegovernance and effectiveness.

Qualifications

Education:

• Bachelor’s degree in Regulatory Affairs, Quality, Engineering, Life Sciences, Supply Chain, ora relateddiscipline (required).

• Advanced degree in a scientific or regulatory field (preferred).

Experience and Skills:

Required:

• Typically4-6 years of experience in Regulatory Compliance, Quality, Supply Chain, or related roles within a regulated industry.

• Working knowledge of regulatory and quality requirementsimpactingsourcing and supplier operations.

• Experience supporting supplier audits, inspections, or compliance assessments.

• Ability to manage complex compliance topics and documentation with strong attention to detail.

• Strong analytical, organizational, and problem‑solving skills.

• Effective written and verbal communication skills.

Preferred:

• Experience in medical devices, healthcare, or other highly regulated industries.

• Familiarity with EMEA regulatory and supplier compliance expectations.

• Experience working in a global or matrixed organization.

• Exposure to regulatory inspections involving supplier or contract manufacturing oversight.

• Quality or Regulatory certifications (e.g., RAC, ASQ).

Other:

• Language: Englishrequired;additionalEuropean languages preferred.

• Travel: Limited; occasional regional travel within EMEA.

• Certifications: Quality or Regulatory certifications preferred but notrequired

For more information on how we support the whole health of our employees throughout their wellness,careerand life journey, please visit www.careers.jnj.com

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.

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