Johnson & Johnson

Senior Quality Systems Analyst

Johnson & Johnson$94K — $151K *
US-AnywhereRemote in Raynham, MA
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, Science, Business, Quality, Regulatory Compliance or related fields.
  • 7 years in regulated healthcare, medical devices, pharmaceuticals, or quality systems environments.
  • Knowledge of FDA regulations, ISO 13485, and ISO 9001 standards.
  • Experience with quality system IT platforms like Windchill, ETQ, DMS, LMS, etc.
  • Strong communication, collaboration, and critical thinking skills.

Responsibilities

  • Support quality systems and compliance activities for DePuy Synthes Commercial Quality.
  • Compile and summarize quality data for reporting and management review.
  • Coordinate document control and training activities effectively.
  • Maintain quality records including assessments and documentation.
  • Assist in nonconformance, CAPA, and quality planning activities.
  • Communicate changes in procedures and training requirements to partners.
  • Support audit readiness and response efforts.

Benefits

  • 401(k) retirement and savings plan participation.
  • 120 hours of vacation per year.
  • 40-56 hours of sick time based on residence state.
  • 13 days of holiday pay, including floating holidays.
  • Up to 40 hours of personal and family time.
  • Parental leave of 480 hours for new parents.
  • 240 hours for bereavement leave for immediate family members.
Full Job Description
Job Function:
Quality

Job Sub Function:
Quality Systems

Job Category:
Professional

All Job Posting Locations:
Raynham, Massachusetts, United States of America, Remote (US)

Job Description:

Johnson & Johnson is currently recruiting for Senior Quality Systems Analyst-US Last Mile! This position can be performed remotely within United States. Remote work may be considered on a case-by-case basis and if approved by the business.

Position Summary:

The Sr Quality Systems Analyst executes quality system activities supporting US DePuy Synthes Commercial Quality (CQ), distribution sites, regional functions, and Last Mile field inventory managers. The role is responsible for supporting quality system data review, metrics reporting, document management, training process execution, and compliance activities that help maintain an effective Quality Management System for commercial activities in the US

Key responsibilities:
  • Support CQ and business partners on quality systems and compliance activities.
  • Compile and summarize quality data for reporting, Data Review Board, and Management Review.
  • Coordinate document control and training activities, including routing, release, assignments, completion monitoring, and records review.
  • Maintain quality records, including gap assessments, risk assessments, inspection tools, and related documentation.
  • Support nonconformance/CAPA, quality planning, change management, and effectiveness monitoring activities.
  • Communicate procedure changes, training requirements, quality expectations, and document updates to cross-functional partners.
  • undefined


Execute and support systems/processes in the following areas:
  • Quality metrics and governance reviews
  • Training and document control processes
  • Audit/inspection readiness and response
  • Quality planning, change management, and risk-based assessments
  • Quality issue and effectiveness monitoring
  • Quality system applications, including DMS, LMS, QEM, ETQ, Windchill, Summit, Compliance Wire, ERP, and warehouse management systems
  • GxP coaching and guidance for business partners

External and internal interactions:
  • DePuy Synthes Quality & Regulatory Compliance
  • DePuy Synthes Commercial/Sales Operations and Supply Chain partners
  • DePuy Synthes external Sales Agents
  • Notified bodies, health authorities, and state regulatory agencies as applicable
  • Other internal or external partners supporting compliant commercial distribution and field inventory operations. (i.e. Marketing)


Required Qualification and Core Competencies for the role:
  • Minimum bachelor's degree required. Preferred degree areas include Engineering, Science, Business, Quality, Regulatory Compliance, or related fields. Associate degree with relevant regulated industry experience may be considered.

Experience:
  • 7 years of relevant work experience in a regulated healthcare, medical device, pharmaceutical, consumer products, distribution, commercial quality, or quality systems environment.
  • Working knowledge of applicable FDA regulations, ISO 13485, ISO 9001, and quality system requirements relevant to commercial distribution and field inventory environments.
  • Experience supporting quality systems, document control, training compliance, quality metrics, audits, nonconformance management, corrective action processes, or related compliance activities.
  • Experience using quality system IT platforms such as Windchill, ETQ, DMS, LMS, QEM, Summit, change control systems, ERP systems, warehouse management systems, or related tools preferred.

Required skills and certifications:
  • Communicate and collaborate effectively with cross-functional partners.
  • Follow established procedures, complete assigned work accurately and on time, maintain organized records, and escalate issues when needed.
  • Apply critical thinking, problem-solving, and root cause analysis to support issue resolution.
  • Demonstrate working knowledge of standard quality system requirements and documentation practices.
  • Use Microsoft Office, data analysis and quality system applications
  • Preferred experience with Windchill, ETQ, Summit, ERP or warehouse management systems.
  • Preferred data analysis experience includes pivot tables, lookups, Power BI, Tableau, or related visualization tools.
  • Preferred experience includes audit preparation, inspection readiness, regulatory responses, or health authority interactions.
  • Preferred certifications or training include Lean, Six Sigma, 5S, ASQ, ISO-13485, Good Distribution Practices, supplier quality, or other quality improvement methods.

Job location: United States: Domestic travel up to 25% may be required based on business needs.

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is :
$94,000.00 - $151,800.00

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.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
NASDAQ

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