Metrology Tech I
Legend Biotech
August 29, 2026
On-site
Raritan, NJ
Operations
Role Overview:
Metrology Tech for cGMP Clinical and Commercial Cell Therapy Manufacturing. Support safe and compliant manufacturing under cGMP, including calibration and instrumentation readiness for daily production and commercial supply; partner across functions to enable robust production, testing, and product release.
Key Responsibilities:
- Provide technical expertise for calibration program; plan/coordinate/execute daily calibration and instrumentation activities.
- Ensure availability of materials, tools, standards, parts, and spares.
- Review/approve/close work orders; manage third-party vendor work per procedures.
- Coordinate calibration during shutdowns; manage IFM calibration outcomes and review CPI/KPI/GPI.
- Develop calibration data sheets, metrology job plans, and master plans.
- Support emergency response and other safety programs.
- Create/track metrology SOPs, quality events, CAPAs, and out-of-tolerance (OOT) documentation.
- Perform risk mitigation and advanced troubleshooting to identify root causes and corrective actions.
- Support calibration interval optimization (including interval extension tasks).
- Define user requirements for new instruments; provide startup/commissioning and qualification/validation support; perform on-the-floor troubleshooting.
- Participate in regulatory and internal audits; manage contractor relationships for quality/compliance.
- Improve metrics across EHS, quality, compliance, cost, delivery, and people.
Requirements:
- B.Sc./M.Sc. in Biological/Biochemical Science/Bioengineering; Trade/Technical School certification (or equivalent); military equivalent acceptable.
- 4+ years cGMP cleanroom manufacturing (aseptic conditions).
- Metrology/calibration and instrumentation knowledge; automation PLCs, VFDs, electrical practices; hands-on cGMP/EHS/regulatory experience (EPA/OSHA/DEA).
- Experience in a fast-paced growth environment; matrix leadership; strong communication, analytical, problem-solving, and project/change management skills.
- CMMS experience; EHS/regulatory standards knowledge.
- Able to manage shifting priorities and lead with influence.
Benefits and Paid Time Off (per job posting):
- Medical, dental, vision; 401(k) with full vesting on day one; 8 weeks paid parental leave after 3 months; PTO (vacation, personal, sick, floating holidays) and 11 company holidays.
- Base pay range: $83,711–$109,870.
- Other voluntary benefits include flexible spending/HSAs, life/AD&D, short-/long-term disability, legal assistance, and supplemental plans; commuter and well-being programs.
Application Instructions:
- Applicants must be authorized to work in the U.S.; employment eligibility verified via E-Verify (Form I-9 required if selected).
Metrology Tech for cGMP Clinical and Commercial Cell Therapy Manufacturing. Support safe and compliant manufacturing under cGMP, including calibration and instrumentation readiness for daily production and commercial supply; partner across functions to enable robust production, testing, and product release.
Key Responsibilities:
- Provide technical expertise for calibration program; plan/coordinate/execute daily calibration and instrumentation activities.
- Ensure availability of materials, tools, standards, parts, and spares.
- Review/approve/close work orders; manage third-party vendor work per procedures.
- Coordinate calibration during shutdowns; manage IFM calibration outcomes and review CPI/KPI/GPI.
- Develop calibration data sheets, metrology job plans, and master plans.
- Support emergency response and other safety programs.
- Create/track metrology SOPs, quality events, CAPAs, and out-of-tolerance (OOT) documentation.
- Perform risk mitigation and advanced troubleshooting to identify root causes and corrective actions.
- Support calibration interval optimization (including interval extension tasks).
- Define user requirements for new instruments; provide startup/commissioning and qualification/validation support; perform on-the-floor troubleshooting.
- Participate in regulatory and internal audits; manage contractor relationships for quality/compliance.
- Improve metrics across EHS, quality, compliance, cost, delivery, and people.
Requirements:
- B.Sc./M.Sc. in Biological/Biochemical Science/Bioengineering; Trade/Technical School certification (or equivalent); military equivalent acceptable.
- 4+ years cGMP cleanroom manufacturing (aseptic conditions).
- Metrology/calibration and instrumentation knowledge; automation PLCs, VFDs, electrical practices; hands-on cGMP/EHS/regulatory experience (EPA/OSHA/DEA).
- Experience in a fast-paced growth environment; matrix leadership; strong communication, analytical, problem-solving, and project/change management skills.
- CMMS experience; EHS/regulatory standards knowledge.
- Able to manage shifting priorities and lead with influence.
Benefits and Paid Time Off (per job posting):
- Medical, dental, vision; 401(k) with full vesting on day one; 8 weeks paid parental leave after 3 months; PTO (vacation, personal, sick, floating holidays) and 11 company holidays.
- Base pay range: $83,711–$109,870.
- Other voluntary benefits include flexible spending/HSAs, life/AD&D, short-/long-term disability, legal assistance, and supplemental plans; commuter and well-being programs.
Application Instructions:
- Applicants must be authorized to work in the U.S.; employment eligibility verified via E-Verify (Form I-9 required if selected).