Entry-Level Manufacturing Engineer — Medical Devices

huMannity Medtec; Santa Clarita (CA); On-site; USD 75,000 - 95,000; Full time

Job summary

huMannity Medtec in Santa Clarita, CA, is seeking a Manufacturing Engineer I to support development, transfer, and production of implantable medical devices. This role collaborates with Manufacturing, R&D, Quality, Supply Chain, and Facilities to ensure scalable, compliant processes.

The ideal candidate enjoys hands-on problem solving in a cross-functional setting and will drive continuous improvement while aligning with GMP and ISO 13485 requirements.

Qualifications

• Bachelor's degree in engineering or related field required.
• 1+ years of engineering experience in manufacturing or related area.
• Experience interpreting engineering drawings and CAD models.
• Proficient with Microsoft Office (Excel, Word, PowerPoint).
• Strong analytical and problem-solving abilities.
• Excellent written and verbal communication skills.
• Highly organized and detail-oriented.

Responsibilities

• Support New Product Introduction (NPI) and transfer activities for implantable devices.
• Develop, validate, and improve manufacturing processes; support IQ/OQ/PQ.
• Create and maintain SOPs, PFMEAs, and process specifications.
• Assist with production planning, workflow optimization, and manufacturing efficiency.
• Troubleshoot equipment and process issues using root cause analysis.
• Support GMP/ISO quality compliance and audits.

Skills

SolidWorks

AutoCAD

Analytical thinking

Troubleshooting

Communication skills

Attention to detail

Team player

MS Office

Education

Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Biomedical Engineering, Materials Engineering, or related field

Tools

SolidWorks

AutoCAD

Job description

huMannity Medtec in Santa Clarita, CA, is seeking a Manufacturing Engineer I to support development, transfer, and production of implantable medical devices. This role collaborates with Manufacturing, R&D, Quality, Supply Chain, and Facilities to ensure scalable, compliant processes.

The ideal candidate enjoys hands-on problem solving in a cross-functional setting and will drive continuous improvement while aligning with GMP and ISO 13485 requirements.