Quality Engineer III - 26-01827

Primary Skills:  Document Control [intermediate], SAP [beginner], ISO 13485 [intermediate], FDA QSRs [intermediate], MS Office Suite [advanced]
Contract Type: W2 Only
Duration: 12+ Months
Location: Santa Clara, CA 95054 (Onsite)
Pay Range: 50.00 – 56.50 per hour on W2
 
Job Summary:
This role focuses on supporting design transfer activities by generating and refining technical documentation. The Quality Engineer will collaborate with R&D and other departments to transition designs into operational instructions and manage all associated quality documents. A key aspect involves identifying and implementing quality improvements by ensuring root causes of issues are resolved and corrective actions are implemented.
 
Key Responsibilities:

• Author and revise technical documents for design transfer.
• Translate technical information into clear work instructions.
• Develop new layouts for manufacturing process documents.
• Input part numbers and Bill of Materials into MRP software.
• Drive cross-functional documentation projects.

Must-Have Skills:

• Experience with Design Control processes.
• Proficiency in creating manufacturing documentation.
• Strong attention to detail and accuracy.
• Experience in the In Vitro Diagnostics (IVD) manufacturing industry is required.

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