Manager, Compliance Risk Management

About this role

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 Systems

Job Category: Professional

All Job Posting Locations: Palm Beach Gardens, Florida, United States of America, Raritan, New Jersey, United States of America, Raynham, Massachusetts, United States of America, Warsaw, Indiana, United States of America

Job Description: DePuy Synthes is recruiting for position, located in MA Raynham , FL Palm Beach Gardens, ,IN Warsaw , NJ Raritan.  Alternate Hybrid locations may be considered at Leeds ,UK or Loughbeg, Ringaskiddy;

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):

MA Raynham :  Requisition Number:  R-094623

St. Anthony's Road, Leeds, UK - Requisition Number:   R-095616

Loughbeg, Ringaskiddy - Requisition Number: R-095618

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 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 o

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