Legend Biotech US

IT Validation Specialist

Legend Biotech US · Somerset, New Jersey, United States

Posted 20 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
20 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 IT Validation Specialist at Legend Biotech will support and execute validation activities for GxP-regulated computerized systems, ensuring compliance with regulatory requirements. Daily responsibilities include authoring and maintaining validation documentation, performing risk assessments, coordinating validation testing, and assisting during audits. The role requires collaboration with IT, Quality Assurance, and vendors to maintain validated systems throughout their lifecycle.

Our read on this posting3.0out of 5
benefits
3/5
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 a Life Science, IT, Engineering or a related field
  • 1-3 years of hands-on experience in Computer System Validation (CSV) within the biotech or pharmaceutical industries
  • Knowledge and understanding of GxP regulations (FDA 21 CFR Part 11, EU Annex 11, GAMP 5, Data Integrity requirements)
  • Experience in applying risk-based methodologies for CSV/CSA
  • Strong interpersonal, oral and written communication skills

Nice to have

  • Experience with Computer Software Assurance (CSA) and AI
  • Experience utilizing an automated Validation Lifecycle Management System (VLMS)
  • Validation of AI and/or use of AI in validation activities in a GxP environment
  • Familiarity with use of electronic systems for Quality Management (QMS), Validation Lifecycle Management (VLMS), and Document Management (EDMS)

What you get

  • Medical, dental, and vision insurance
  • 401(k) retirement plan with a company match that vests fully on day one
  • Eight (8) weeks of paid parental leave after three (3) months of employment
  • Paid time off policy including vacation time, personal time, sick time, floating holidays, and eleven (11) 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 such as pet, critical illness, accident, and hospital indemnity insurance
  • Voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs

Worth weighing

  • No specific mention of remote work options, though a hybrid model is indicated
  • The role requires compliance with strict GxP regulations, which may involve high-pressure situations during audits
  • Experience with specific systems like ValGenesis and Veeva Quality Vault is preferred but not mandatory

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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