DePuy Synthes is recruiting for a(n) Lead MSA SOP Strategy & Compliance Leader,locatedininWest Chester, PA,Raynam, MA, Warsaw, IN, Palm Beach Gardens, FL or Leeds, UK

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

US - Requisition Number: R-071882

UK - Requisition Number: R-073360

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Johnson & Johnson announced plans to separate our Orthopedics business toestablisha standalone orthopedics company,operatingas 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 berequired, 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 plans. In that case, details of any planned changes would be provided to you by DePuy Synthes atan appropriate timeand subject to any necessary consultation processes.

The Lead MSA SOP Strategy & Compliance Leader roleis responsible forshaping and governing the strategic direction of Standard Operating Procedures (SOPs) across DePuy Synthes Medical and Scientific Affairs (MSA), with a strong focus on external regulatory, industry, and compliance environments. This role plays a leadership function in ensuring SOP strategiesremainaligned with evolving global regulations, industry standards, and business priorities while enabling operational excellence across the organization.

This is an impactful role for a strategic leader who enjoysoperatingat the intersection of regulatory intelligence, enterprise SOP governance, andcross‑functionalcollaboration in a highly regulated medical technology environment.

Key Responsibilities

• Continuouslymonitorthe external environment for global regulations, standards, and guidance related to clinical trial conduct, as well as Clinical Evaluation Reports (CERs) and Summary of Safety and Clinical Performance (SSCPs).

• Serve as a single point of contact and coordinate with subject matter experts in the Clinical & Medical Affairs teams to support internal and external audits by providing SOP documentation andevidence, coordinating responses to audit observations, and ensuringtimelycompletion of related corrective and preventive actions (CAPAs) as applicable

• Assess regulatory and guidance changes for applicability and business impact; summarize implications and recommended actions for MSA SOP strategy and operational execution.

• Serve as the primary liaison between external regulatory intelligence and internal SOP owners to ensuretimelyawareness, alignment, and decision-making.

• Establish, operationalize, and oversee the MSA SOP governance process (charter, roles/responsibilities, meeting cadence, decision rights, and documentation expectations).

• Drive strategic input and alignment from key governance functions, including Clinical Research/Operations, Scientific Operations (CER strategy & writing), and Medical Affairs, as well as other cross-functional stakeholders as needed.

• Maintain a forward-looking SOP update roadmap and prioritize revisions based on regulatorychangedrivers, risk, and business needs.

• Oversee end-to-endlogisticsand project management for SOP updates, including coordinating drafting, redlines/markups, version control, and consolidation of feedback.

• Coordinate communication andimplementationsupport for SOP changes (e.g., release planning, stakeholder notifications, and readiness activities) in partnership with SOP owners.

• May be assigned responsibilities related to study resourcing and project management responsibilities, asrequired

• Provide input on study specific documents as requested, such as protocol, informed consent, ISO 14155 gap assessments,etc

Qualifications

Education

• Bachelor’s degreerequired(e.g., Business, Science, Engineering, Quality, Regulatory, or related field).

• Advanced degree (e.g., Master’s, MBA, or equivalent) preferred.

Experience and Skills

Required:

• Typically requires 6-8 years of progressive experience in Clinical Research/Operations or Regulatory, with exposure to SOP governance, quality systems, regulatory strategy, or related functions (e.g., medical devices, pharmaceuticals, life sciences).

• Experience supporting external audits and inspection readiness

• Demonstrated experience leading SOP or management system strategy at an enterprise or global level.

• Strong understanding of global regulatory and external compliance environments.

• Experience working in complex, matrixed organizations.

• Knowledge and application of clinical regulations and standards applied in different clinical areas and regions isrequired

Preferred:

• Experience within a medical device or MedTech organization.

• Familiarity with global quality system standards and regulatory frameworks.

• Experience supportinglarge‑scaletransformation or system implementation initiatives.

• Demonstrated ability to interpret external regulations or guidancedocuments, andtranslate them into practical SOP strategies.

• Experience working in global ormulti‑regionalroles.

• Proven ability to leadcross‑functionalinitiatives and influence stakeholders without direct authority.

• Excellent strategic thinking,problem‑solving, anddecision‑makingskills.

• Strong written and verbal communication skills, with experience presenting to senior leaders.

Other

• Language:Proficiencyin Englishrequired

• Travel: Up to 10%, domestic and/or international.

• Certifications: Quality, Regulatory, or Compliance 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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