Johnson & Johnson

Preclinical Compliance Associate

Johnson & Johnson$92K — $148K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree required
  • 2+ years of relevant experience
  • Experience managing medical programs within timelines and budgets
  • Strong understanding of SOPs and compliance regulations
  • Willingness to travel up to 25% domestically and internationally

Responsibilities

  • Coordinate CRO strategies and execution
  • Develop and enforce Standard Operating Procedures (SOPs)
  • Implement and manage safety programs including CAPA processes
  • Manage maintenance and calibration schedules for equipment
  • Onboard and qualify external labs and service providers
  • Manage outsourcing relationships and vendor communications
  • Optimize lab scheduling and resource allocation
  • Procure lab materials and manage related budgets

Benefits

  • Vacation - 120 hours per year
  • Sick time - 40 to 56 hours per year depending on location
  • Holiday pay - 13 days per year
  • Parental Leave - 480 hours for new parents
  • Caregiver Leave - 80 hours in a rolling 52-week period
  • Volunteer Leave - 32 hours per year
  • Military Spouse Time-Off - 80 hours per year
Full Job Description
Job Function:
Discovery & Pre-Clinical/Clinical Development

Job Sub Function:
Biological Research

Job Category:
Scientific/Technology

All Job Posting Locations:
Irvine, California, United States of America

Job Description:

Johnson & Johnson MedTech, Electrophysiology, is recruiting a Preclinical Compliance Associate This position is located in Irvine, CA and will be following a hybrid model.

Purpose: The Preclinical Compliance and Planning Associate will drive contract-research lab strategies, ensure compliance with all internal and external animal welfare requirements, collaborate on strategic partnerships, manage project timelines, and oversee process improvements to improve the functioning of the Preclinical Research Department.

You will be responsible for:
  • Act as primary coordinator for CRO strategy and execution: evaluate when to outsource vs. perform work internally, select vendors, and manage study handoffs and timelines.
  • Develop, review, and enforce Standard Operating Procedures (SOPs)
  • Design, implement, and manage chemical, biological, and radiological safety programs, including CAPA (corrective and preventive action) processes.
  • Manage preventive maintenance, calibration, and service schedules for critical equipment (e.g., biosafety cabinets, anesthesia systems, radiology devices).
  • Identify, qualify, and onboard external laboratories and service providers using a structured supplier qualification process and required documentation.
  • Manage outsourcing relationships and vendor communications to ensure deliverables meet scientific, quality, and compliance expectations.
  • Serve as the lab scheduling and resource-allocation lead to optimize facility usage, reduce bottlenecks, and support project timelines.
  • Coordinate procurement for lab usage and research materials: generate purchase requests, manage budgets, and track expenses with finance partners.
  • Monitor and manage finance/budget aspects for preclinical operations, including forecasting, tracking spend vs. plan, and identifying cost-saving opportunities.
  • Create and maintain job descriptions and role expectations for preclinical staff; support hiring and onboarding processes.
  • Track and report key performance indicators (KPIs) and operational metrics (e.g., study throughput, animal census, equipment uptime, training compliance) to leadership.
  • Maintain an annual calendar of important regulatory, accreditation, and operational milestones to ensure proactive planning and timely submissions.
  • Manage documentation control, record retention, and data integrity practices to support audits and reproducible science.
  • Drive continuous improvement initiatives across operations, quality, and compliance, and lead cross-functional corrective/preventive actions.


Qualifications / Requirements:
  • A minimum of a Bachelor's Degree
  • A minimum of 2 years of relevant experience is required
  • Proven track record of contributing to medical programs on time, within budget and in compliance to SOPs and regulations is required.
  • Up to 25% domestic and international travel may be required.


Required Skills:

Preferred Skills:
Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Coaching, Collaboration, Communication, Critical Thinking, Data Analysis, Data Savvy, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Product Development Lifecycle, Report Writing, Stakeholder Engagement, Technologically Savvy

The anticipated base pay range for this position is :
$92,000.00 - $148,350.00

Additional Description for Pay Transparency:
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
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141,700 employees
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$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
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