Associate Director, Quality Systems
Legend Biotech US · Raritan, New Jersey, United States
Posted about 2 months 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
- 57 days Legend Biotech US's roles stay open a median of 76 days
- Reposted
- No
- Salary listed
- No 0% of Legend Biotech US's roles list one
- Ghost-job risk at Legend Biotech US
- high 78 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
- 2026-10-23
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.
- 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 2026-10-23. PitchMeAI is not the employer.
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