Senior Equipment Technician – GMP Medical Device Maintenance

Penumbra, Inc.; Roseville (CA); On-site; USD 50,000 - 69,000; Full time

Benefits offered by this job

Medical, dental, vision, life, AD&D

Short & long-term disability insurance

401(k) with employer match

Paid parental leave

11 paid company holidays

Min 15 days vacation per year

Paid sick time

Job summary

Penumbra, Inc. is seeking an Equipment Technician III to set up and maintain manufacturing and test equipment in a GMP environment. This role includes documenting activities, training new technicians, and collaborating with engineering on improvements.

The position requires 5+ years in a medical device/manufacturing setting, strong communication, and proficiency with common Office tools. On-site work with potential overtime and weekend availability is expected.

Qualifications

• Must have 5+ years in medical device or manufacturing environment.
• Experience building, troubleshooting, repair and maintenance of manufacturing equipment per GMP guidelines.

Responsibilities

• Perform preventive, on-demand and non-standard maintenance with proper documentation.
• Collaborate with technicians and guide others in maintenance and troubleshooting.
• Install equipment and complete IQ/OQ validation to ensure functionality.
• Manage spare parts inventory and reorder as needed.
• Train equipment technicians on repairs and departmental practices.
• Support manufacturing lines and participate in line moves and relocations.
• Suggest equipment/fixture improvements and draft related documentation.

Skills

Strong communication

Attention to detail

Organizational skills

MS Office proficient

Education

High School or GED + 5+ years experience

Associate degree preferred

Tools

Outlook

MS Word

Excel

PowerPoint

Job description

Penumbra, Inc. is seeking an Equipment Technician III to set up and maintain manufacturing and test equipment in a GMP environment. This role includes documenting activities, training new technicians, and collaborating with engineering on improvements.

The position requires 5+ years in a medical device/manufacturing setting, strong communication, and proficiency with common Office tools. On-site work with potential overtime and weekend availability is expected.