Manufacturing Operator II
Kyowa Kirin North America(26 days ago)
About this role
The Manufacturing Operator II supports a greenfield biopharmaceutical site focused on rare disease therapies, participating in start-up and execution of core manufacturing operations. This individual contributor role reports to the Manager, Manufacturing and supports commissioning, validation, and transition to routine production while working closely with engineering, automation, and quality teams. The position is based onsite in Sanford, NC and will follow construction-phase day shift then transition to a rotating 2-2-3 day shift once operational. Travel up to 10% may be required and training at the Japan site may occur during start-up.
Required Skills
- GMP Compliance
- Biomanufacturing
- Upstream Processing
- Downstream Processing
- Equipment Commissioning
- Process Validation
- Automation Implementation
- Troubleshooting
- Continuous Improvement
- Regulatory Compliance
+24 more
Qualifications
- Bachelor’s Degree in Technical or Scientific Discipline
- Associate Degree in Technical Field
- High School Diploma or Equivalent
About Kyowa Kirin North America
kyowakirin.comKyowa Kirin is a Japanese biopharmaceutical company that develops innovative specialty medicines, with a particular focus on antibody‑based therapies for cancer, kidney disease, and immune‑mediated disorders. The company pursues technology‑driven drug discovery across biologics and small molecules and maintains a broad global network of research, development, and commercial operations. Kyowa Kirin advances a pipeline through internal R&D and strategic partnerships (including biologics and CDMO collaborations) to bring life‑changing treatments to patients. It emphasizes patient‑centred value, scientific expertise, and sustainability in its mission to raise health and well‑being worldwide.
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