Johnson & Johnson

Manager, Compliance Risk Management

Johnson & Johnson$153K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in engineering, life sciences, or related field required; advanced degree preferred.
  • 6-8 years of experience in Quality Assurance, Compliance, or Risk Management within a regulated industry, preferably medical devices.
  • Strong grasp of quality systems, compliance risk management, and regulatory standards.
  • Experience with audits, inspections, and compliance-related activities is essential.
  • Ability to analyze data and present actionable risk assessment recommendations clearly.
  • Effective at collaborating across teams in matrixed organizations.

Responsibilities

  • Lead compliance risk management efforts, including risk identification, assessment, and mitigation.
  • Develop processes for risk management that align with regulatory requirements.
  • Collaborate with various teams to embed risk-based thinking into operations.
  • Assist with internal and external audits by preparing necessary documentation and risk assessments.
  • Analyze quality data to identify compliance risks and improvement opportunities.
  • Provide training on compliance principles and quality expectations.
  • Ensure comprehensive documentation and reporting on compliance risks.
  • Drive initiatives for continuous improvement in compliance and quality.

Benefits

  • Comprehensive retirement plan (pension) and 401(k) savings plan participation.
  • Generous vacation policy, with 120 hours annually.
  • Flexible sick time and family leave options, including 480 hours for parental leave.
  • Volunteer leave program allowing 32 hours per year.
  • Support for military spouses with dedicated time-off.
Full Job Description
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 our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

#LI-Hybrid

#DePuySynthesCareers

Required Skills:

Preferred Skills:
Analytical Reasoning, Analytics Dashboards, Collaboration, Compliance Management, Data Gathering and Analysis, Data Quality, Incident Management, Performance Measurement, Process Improvements, Quality Control (QC), Quality Management Systems (QMS), Quality Services, Quality Standards, Risk Management, System Integration, Systems Analysis, Tactical Planning, Technical Credibility

The anticipated base pay range for this position is :
153,000.00 USD Annual

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.careers.jnj.com/employee-benefits

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
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