Manager, Compliance Risk Mgmt.

Job title Manager, Compliance Risk Mgmt. Function Quality Sub function Quality & Compliance Audit Category Manager, Quality & Compliance Audit (P7) Location Raynham / United States of America Date posted May 21 2026 Requisition number

R-074950

Work pattern Hybrid Work This job posting is anticipated to close on Jun 01 2026. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications. Description At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality Job Sub Function:

Quality & Compliance Audit Job Category:

Professional All Job Posting Locations:

Raynham, Massachusetts, United States of America Job Description:

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and 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 at an appropriate time and subject to any necessary consultation processes DePuy Synthes is recruiting for a(n) Manager, Compliance Risk Management, located in Raynham, MA. Johnson & Johnson announced plans to separate our Orthopedics business to establish a standalone orthopedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and 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 at an appropriate time and subject to any necessary consultation processes. Job Overview The Manager, Compliance Risk Management is a Quality Assurance leadership role responsible for identifying, assessing, and managing compliance risks across DePuy Synthes operations. This role plays a key part in ensuring adherence to quality system requirements and regulatory expectations while enabling business execution. The position partners closely with Quality, Regulatory, Manufacturing, Supply Chain, and other cross‑functional teams to proactively manage risk, support inspections, and strengthen a culture of quality and compliance. Key Responsibilities Lead compliance risk management activities, including identification, assessment, mitigation, and monitoring of quality and regulatory risks. Develop and maintain risk management processes aligned with quality system and regulatory requirements. Partner with cross‑functional teams to integrate risk‑based thinking into operational and quality decision‑making. Support internal and external audits and inspections by preparing risk assessments, documentation, and responses. Analyze trends, metrics, and quality data to identify emerging compliance risks and improvement opportunities. Provide guidance and training on compliance risk management principles and quality system expectations. Ensure effective documentation and reporting of compliance risks and mitigation actions. Drive continuous improvement initiatives to enhance compliance risk processes and overall quality system effectiveness. Communicate risk status, priorities, and recommendations to Quality and business leadership. Qualifications Education Bachelor's degree required in engineering, life sciences, or a related technical discipline. Advanced degree preferred.

Experience and Skills Required:

6-8 years of progressive experience in Quality Assurance, Compliance, or Risk Management within a regulated industry (medical device preferred). Strong knowledge of quality systems, compliance risk management, and regulatory expectations. Experience supporting audits, inspections, and compliance‑related activities. Demonstrated ability to assess risk, analyze data, and translate findings into actionable recommendations. Proven ability to work effectively in cross‑functional and matrixed environments. Strong written and verbal communication skills, with the ability to influence and engage stakeholders.

Preferred:

Experience in medical device quality systems and global regulatory environments. Prior people leadership or project leadership experience. Experience with risk management tools, methodologies, and quality metrics. Demonstrated success driving continuous improvement initiatives. Familiarity with FDA, ISO, and other applicable quality and regulatory standards.

Other:

Languages:

English required.

Travel:

Moderate, primarily domestic.

Certifications:

Quality or compliance‑related certification (e.g., ASQ, RAC) preferred. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com . .

Required Skills:

Preferred Skills:

Agile Internal Audit, Analytical Reasoning, Audit and Compliance Trends, Compliance Frameworks, Compliance Management, Compliance Policies, Compliance Risk, Critical Thinking, Process Improvements, Quality Auditing, Quality Control (QC), Quality Standards, Regulatory Compliance, Risk Management, Technical Credibility, Third-Party Auditing The anticipated base pay range for this position is : $102,000.00

• $177,100.

00 Additional Description for

Pay Transparency:

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 period10 days Volunteer Leave
• 32 hours per calendar year Military Spouse Time-Off
• 80 hours per calendar year For additional general information on Company benefits, please go to:
• https://www.

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