×
Register Here to Apply for Jobs or Post Jobs. X

Associate Director, Quality Systems

Job in Raritan, Somerset County, New Jersey, 08869, USA
Listing for: Legend Biotech USA
Full Time position
Listed on 2026-09-07
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Data Analyst
Salary/Wage Range or Industry Benchmark: 150000 - 210000 USD Yearly USD 150000.00 210000.00 YEAR
Job Description & How to Apply Below

Legend Biotech is seeking an Associate Director, Quality System
s as part of the Quality team based in Raritan, NJ.

Role Overview

The Associate Director, Quality Systems is a member of the Raritan Quality Leadership Team with responsibilities for quality systems oversight within a cell therapy manufacturing plant to support commercial requirements in a sterile GMP environment. This role will oversee a team of quality systems specialists responsible for managing systems and associated processes and procedures, including document control, investigations, CAPA, change control, site quality metrics, and laboratory QA oversight.

They will also support site quality compliance, including site inspection readiness and support during regulatory inspections.

Key Responsibilities
  • Provide quality systems oversight for the CAR-T manufacturing site
  • Responsible for oversight of Quality Systems, Systems Support, and Investigations teams to meet goals and deadlines.
  • Ability to manage multiple and complex projects, provide status reports, and coordinate with other departments
  • Manage cross-functional projects with many stakeholders and collaborate with functional departments to resolve issues.
  • Require minimal direction to complete tasks, knows how to get resources and information from established internal contacts; consult with supervisor for decisions outside established processes.
  • Identify efficiencies within the teams to enhance compliance and improve productivity.
  • Lead the implementation and continuous improvement of Quality Risk Management (QRM) processes in accordance with applicable regulatory requirements and site procedures
  • Facilitate cross-functional risk assessments (e.g., FMEA, hazard analysis, impact assessments) to identify, evaluate, and mitigate quality, compliance, and operational risks.
  • Ensure risks associated with investigations, deviations, CAPAs, changes, and process improvements are appropriately assessed, documented, and monitored through closure.
  • Monitor quality trends, recurring events, backlog metrics, and emerging signals to proactively identify systemic risks and recommend preventive actions.
  • Partner with Manufacturing, Quality Control, Engineering, Supply Chain, and Technical Operations to harmonize procedures, processes and systems, and drive risk-based decision making across site operations.
  • Present key quality and compliance risks, mitigation strategies, and risk trends to site leadership and governance forums.
  • Evaluate the effectiveness of risk controls and CAPAs to ensure sustainable risk reduction and prevention of recurrence.
  • Drive a proactive risk culture by coaching investigators, quality leads, and cross-functional teams on risk identification, assessment methodologies, and mitigation strategies.
  • Utilize quality metrics and analytics to identify high-risk processes, recurring failure modes, and opportunities for continuous improvement.
  • Lead and provide expert guidance for complex, high-risk, critical, and OOS investigations; facilitate investigation strategy meetings and root cause analysis workshops.
  • Review and approve highly complex investigations, CAPAs, corrections, and effectiveness checks to support robust root cause determination and sustainable corrective actions.
  • Monitor, trend, and report investigation and CAPA quality, timeliness, backlog, aging, recurrence, and effectiveness metrics; develop dashboards, KPIs, and performance management tools
  • Lead investigation excellence initiatives focused on investigation quality, cycle time, root cause effectiveness, inspection readiness, and site-wide accountability.
  • Lead governance forums, including Quality Lead meetings, CAPA Forum, and investigation coaching and mentoring sessions.
  • Provide guidance to other employees in the interpretation of quality issues
  • Develop project charters, timelines, resource plans, risk assessments, and success metrics; lead cross-functional teams through implementation and sustainment.
  • Support improvements to procedures, standards, training qualification, coaching, and governance processes; lead maturity assessments and benchmarking activities.
  • Manage strategic and continuous improvement projects supporting process…
Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary