or apply directly on Legend Biotech US's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 59 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 Sr. CQV Specialist at Legend Biotech will be responsible for providing commissioning, qualification, and validation support for the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This role involves managing complex CQV projects, executing protocols, and ensuring compliance with regulations while collaborating with cross-functional teams. The specialist will also train junior team members and present CQV work during audits.
- benefits
- 5/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 4/5
- 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 or equivalent technical discipline
- 7 years relevant work experience
- Experience in an aseptic manufacturing facility, preferably in cell therapy
- Knowledge of cGMP regulations and FDA/EU guidance
- Strong interpersonal and written/oral communication skills
- Ability to process complex information and make critical decisions
Nice to have
- Experience with CAR-T manufacturing or cell processing
- Experience with 21 CFR parts 600, 601, and 610
What you get
- Medical, dental, and vision insurance
- 401(k) retirement plan with company match
- Eight weeks of paid parental leave after three months of employment
- Paid time off policy including vacation, personal, sick time, floating holidays, and eleven company holidays
- Voluntary benefits including flexible spending and health savings accounts
- Life and AD&D insurance
Worth weighing
- No specific mention of remote work options; position may require onsite presence
- The role involves significant responsibility in compliance and regulatory aspects, which may be stressful
- The position requires managing multiple complex projects, which could lead to a high workload
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.
More roles at Legend Biotech US
- QA, Shop Floor Specialist IIRaritan, New Jersey, United States
- Associate Director, Global Scientific Communications, Medical AffairsUnited States
- Sr. Manager, Biostatistician / ProgrammerSomerset, New Jersey, United States
- Scientist I, Analytical DevelopmentSomerset, New Jersey, United States
- Scientist/Sr. Scientist, Bioinformatics DataSomerset, New Jersey, United States
- Sr. Cell Therapy Account Specialist, Boston NorthMassachusetts, USA
- Sr. Manager ServiceNow CMDB & Asset GovernanceBridgewater, New Jersey, United States
- Principal BioinformaticianSomerset, New Jersey, United States