Manager, Source Reg Compliance (EMEA)

Johnson & Johnson announced plans to separate our Orthopedics business toestablisha standalone orthopedics companyoperatingas DePuy Synthes. The process of the planned separation isanticipatedto be completed within 18 to24 months subject to legal requirements including consultation with works councils and other employee representative bodies as may be regulatory approvals and other customary conditions and approvals. Should you accept this position it isanticipatedthat following conclusion of the transaction you would be an employee of DePuySynthesand your employment would be governed by DePuy Synthes employment processes programs policies and benefit that case details of any planned changes would be provided to you by DePuy Synthes atan appropriate timeand subject to any necessary consultation processes.

Job Overview

The Manager Source Regulatory Compliance (EMEA)is responsible forleading regulatory compliance activities related to sourcing suppliers and externally provided processes across the EMEA region. This role ensures that suppliers contract manufacturers and sourced materialscomply withapplicable regulatory requirements quality system standards and internal policies. The position plays a critical 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 multiple countries.

Key Responsibilities

• Execute source regulatory compliance activities including supplier audit execution investigation approval and objective evidence review to ensure adherence to regulatory and quality system requirements

• Provide regulatory 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 monitoring and lifecycle management.

• Interpretglobalregulatory requirements and translate them 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;drive corrective and preventive actions.

• Ensureaccuratemaintenance of compliance documentation records and reports.

• Contributes tocontinuous improvement initiatives to strengthen suppliercompliancegovernance and effectiveness.

Qualifications

Education:

• Bachelors degree inEngineering Life Sciences Supply Chain ora relateddiscipline (required).

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

Experience and Skills:

Required:

• Typically6-8 years of progressive experience in Regulatory Compliance Quality Supply Chain or related roles within a regulated industry.

• Strong working knowledge ofglobalregulatory and quality requirementsimpactingsupplieroperations.

• Experienceleadingsupplier audits inspections and compliance assessments.

• Ability to manage complex compliance topics across multiple countries and stakeholder groups.

Preferred:

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

• Familiarity withglobalregulatory and supplier compliance frameworks.

• 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).

• Strong analytical riskmanagement and problemsolving skills.

• Effective written and verbal communication skills.

Other:

• Language: English;additionalEuropean languages preferred.

• Travel:Moderate regional travel; limited international travel.

• Certifications: Quality or Regulatory certifications preferred but not.

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