| Manufacturing Supervisor – Purification (Albumin) |
| Clayton, NC 27520 |
| Grifols |
| Exposure to extreme cold below 32*, miscellaneous production chemicals, moving machinery and production equipment. 12 Hr Rotating Shift 6a-6p // 6p-6a. |
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| NFF – Fractionation Technician I/II – Night Shift |
| Clayton, NC 27520 |
| Grifols |
| Exposure to miscellaneous production chemicals, moving machinery and production equipment. Monitor status of manufacturing processes. |
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| Program Quality Leader |
| Durham, NC 27703 |
| GE Aerospace |
| Product quality review associated with the manufacturing process. Minimum of 3 years of Product quality review associated with the manufacturing process… |
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| Technical Trainer – Composites Production |
| Morrisville, NC |
| Anduril Industries |
| Minimum of 3 years of hands-on experience as a technician in a relevant manufacturing or production environment. |
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| Principal Validation Engineer, CVRM |
| Holly Springs, NC |
| Genentech |
| Develops, implements and maintains validation status of the application equipment and manufacturing processes. Estimates qualifications needs, material needs and verifies pre requisite completions. |
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| Principal QA Specialist (Assembly & Packaging), CVRM |
| Holly Springs, NC 27539 |
| Genentech |
| You excel at embedding operational excellence in complex, large-scale manufacturing environments. In this role you will be a member of the QA team providing… |
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| Senior QA Specialist, CVRM |
| Holly Springs, NC 27539 |
| Genentech |
| In this role, you will be a member of the QA team providing Quality oversight for all manufacturing and warehouse operational activities. |
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| Principal QA Specialist (Multi-dose pens), CVRM |
| Holly Springs, NC 27539 |
| Genentech |
| Minimum of 8–10 years in a GxP environment, with at least 4 years of cartridge sterile drug product manufacturing experience in either a manufacturing, QA… |
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| Senior Manager, Process and Compliance (Assembly and Packaging) |
| Holly Springs, NC 27539 |
| Genentech |
| You will provide strategic oversight for the governance, validation, and approval framework of manufacturing batch records within the MES system. |
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| Principal Validation Engineer, CVRM |
| Holly Springs, NC 27539 |
| Genentech |
| Develops, implements and maintains validation status of the application equipment and manufacturing processes. Lead and facilitate Risk Assessment sessions. |
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