Legend Biotech US

Associate Director, Quality Systems

Legend Biotech US · Raritan, New Jersey, United States

Posted 21 days ago

or apply directly on Legend Biotech US's site. We never take the application ourselves.

Is this posting real?

This role has been open
21 days
Legend Biotech US's roles stay open a median of 40 days
Reposted
No
Salary listed
No
0% of Legend Biotech US's roles list one
Ghost-job risk at Legend Biotech US
high
36 stale, 2 reposted of 79 open
Hiring momentum
125 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-09-17

Measured from postings appearing on and disappearing from Legend Biotech US's own greenhouse board since 2026-08-03. Full hiring picture for Legend Biotech US.

About this role

The Associate Director, Quality Systems will oversee quality systems within a cell therapy manufacturing plant, ensuring compliance with commercial requirements in a sterile GMP environment. This role involves managing a team responsible for document control, investigations, CAPA, change control, and quality metrics, while also supporting regulatory inspections and site quality compliance. The position requires collaboration across various departments to enhance productivity and compliance through effective risk management and continuous improvement initiatives.

Our read on this posting3.2out of 5
benefits
3/5
freshness
4/5
career value
4/5
role clarity
5/5
pay transparency
0/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Legend Biotech US as an employer.

What you need

  • Bachelor’s degree in Science, Engineering, Biotechnology, Pharmacy, Information Science, Biology, or a related technical discipline
  • Minimum 10 years of Quality experience within a cGMP-regulated manufacturing facility, biotechnology, biopharmaceutical, or Cell & Gene Therapy manufacturing environment
  • Demonstrated experience leading quality systems, complex investigations, CAPA programs, governance programs, quality improvement initiatives, cross-functional projects, and regulatory inspection or audit readiness activities

Nice to have

  • An advanced degree

What you get

  • Medical, dental, and vision insurance
  • 401(k) retirement plan with a company match that vests fully on day one
  • Eight weeks of paid parental leave after three months of employment
  • Paid time off policy including vacation time, personal time, sick time, floating holidays, and eleven company holidays
  • Voluntary benefits including flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans
  • Voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs

Worth weighing

  • No specific mention of the technologies or tools used in quality systems management
  • The role requires minimal direction, which may indicate a high level of autonomy and responsibility
  • The position is based in a sterile GMP environment, which may involve strict regulatory compliance challenges

Summarised from Legend Biotech US's posting. Read the full original.

Listed by Legend Biotech US on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.

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