Legend Biotech
Validation Specialist
$120K
Raritan, New Jersey, United States · Full-time · Posted Oct 7, 2026
- Experience
- 2 years of experience in validation or manufacturing/process/production engineering within the pharmaceutical/biopharma industry.
- Education
- Bachelor’s degree in Industrial Engineering, Manufacturing Engineering, Mechanical Engineering, or a related field.
- Visa sponsorship
- Applicants must be authorized to work in the United States; employment eligibility is verified through E-Verify.
About the job
Executes and oversees site validation, qualification, and process-control activities to keep cell therapy manufacturing processes in a validated state and support technical changes.
What you'll do
- Manage validation activities, including aseptic process validation, particle runs, equipment qualification, and related investigations and reporting.
- Assess changes and risks for validation impact; support raw-material, consumable, packaging, and labeling changes and their associated studies.
- Work across Technical Operations and with external vendors on automation platforms for cell therapy development and manufacturing.
What they ask for
- Bachelor’s degree in Industrial Engineering, Manufacturing Engineering, Mechanical Engineering, or a related field.
- Process validation, equipment qualification, or aseptic processing skills.
- Experience writing or supporting Quality Risk Assessments.
Pay
$120,000 — $120,000 USD (base pay)
Model-written summary · the original posting is authoritative