Johnson & Johnson

Compliance Specialist IV

Johnson & Johnson$134K — $148K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, Life Sciences, or related field.
  • 6 years of relevant experience as a Compliance Specialist IV or in a related role.
  • Experience in Lean management and Quality Assurance.
  • Expertise in audit management and regulatory compliance.
  • Knowledge of FDA regulations and ISO-13485 standards.
  • Proven capability in developing and reviewing Standard Operating Procedures (SOPs).
  • Experience in quality oversight of external sales agents and consignment models.

Responsibilities

  • Develop and manage Quality and Compliance programs for Med Tech US field inventory.
  • Support the delivery of surgical loaner sets to orthopedic customers.
  • Act as a liaison among Quality, Distribution, and Sales to resolve quality issues.
  • Identify and implement improvement opportunities aligned with business objectives.
  • Lead audits, inspections, and investigations for compliance and quality assurance.
  • Ensure regulatory compliance of quality programs across distribution processes.
  • Establish relationships with various partners to adapt to regulatory changes.

Benefits

  • Eligible to participate in a consolidated retirement plan (pension) and 401(k) savings plan.
  • Long-term incentive program participation available.
  • Vacation time of 120 hours per calendar year.
  • Sick time and personal leave options varying by state residency.
  • Comprehensive medical, dental, and vision coverage available.
  • Generous parental leave policy of 480 hours within one year.
  • Volunteer leave of 32 hours per calendar year.
Full Job Description
Job Function:
Quality

Job Sub Function:
Customer/Commercial Quality

Job Category:
Professional

All Job Posting Locations:
New Brunswick, New Jersey, United States of America

Job Description:

Employer: Johnson & Johnson Health Care Systems Inc.

Job Title: Compliance Specialist IV

Job Code:

Job Location: New Brunswick , NJ

Job Type: Full-Time

Rate of Pay: $134,000 - $148,000/year

Job Duties: Develop, execute, and oversee Quality and Compliance (Q&C) programs for Med Tech US field inventory within the North America Region, including Field Inventory Locations (FIL), Field Sales Offices, Loaner Sites, and Distribution Centers (DC). Support "last mile" delivery of surgical loaner sets support joint reconstruction and orthopedic customers across the US. Serve as a liaison with Quality, Distribution, Sales, Commercial, and Supply Chain partners on distribution quality related matters to drive timely resolution of quality related issues. Identify and support implementation of improvement opportunities consistent with business objectives and the Enterprise Quality Standards. Define, implement, and validate quality requirements and systems in alignment with departmental strategies. Participate in and lead audits, inspections, investigations, and remediation activities. Ensure the Quality program maintains regulatory compliance. Provide quality support for existing and new distribution processes. Develop, implement, and review standard operating procedures. Establish and maintain relationships with NA DELIVER, DePuy Synthes Sales Inc., and other Med Tech Franchise customers in order to solve problems and meet changing competitive and regulatory environments. Execute and improve systems/processes in Inspection readiness; Commercial Quality including field inventory consignment and Loaner programs; Process changes; Validation, Calibration, and Preventive Maintenance systems; Delivery service issue trending; and Nonconformance investigation and corrective action plan development, implementation, and effectiveness monitoring.

Requirements: Employer will accept a Bachelor's degree in Engineering, Life Sciences, or related field and 6 years of experience in the job offered or in a Compliance Specialist IV-related occupation.

Position requires experience with:

1. Lean management and Quality Assurance;

2. Quality program leadership;

3. Audit management;

4. Validation and compliance;

5. Standard Operating Procedures (SOPs) development, implementation, and review;

6. Process improvement activities including value-based healthcare, Agile methodology, root cause analysis, statistical process control, and process mapping and reengineering;

7. Quality oversight of external sales agents/consignment models;

8. Health Authority or notified body; and

9. FDA regulations and ISO-13485 standards.

*May telecommute.

*Up to 20% domestic travel required.

This job posting is anticipated to close on 9/17/2026.

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)).

This position is eligible to participate in the Company's long-term incentive program.

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
  • This position is eligible for benefits to include medical, dental, vision and time off, as well as any others as provided for in the applicable Collective Bargaining Agreement.
  • For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits


Required Skills:

Preferred Skills:

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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