Medical Device Assembler I — Cleanroom

Penumbra, Inc.; Reno (NV); On-site; USD 24,796 - 31,684; Full time

Benefits offered by this job

Medical, dental, vision, life, AD&D, &

Job summary

Penumbra, Inc. in Salt Lake City, UT, is seeking a Production Builder I to assemble medical devices in a cleanroom environment on the day shift. Under supervision, you will perform moderately complex assembly, data recording and basic product testing, following QSR/ISO13485 and company SOPs.

Your responsibilities include set-up of manufacturing equipment, in-process inspection, maintaining cleanliness, and ensuring accurate lot records, with training completed and on-site attendance required.

Qualifications

• High school or equivalent required with 1+ year clean room or manufacturing experience.
• Basic math skills and ability to read and follow procedures.
• Able to comprehend spoken and written English; effective communication.
• Attention to detail and high manual dexterity; familiar with cleanroom protocols.
• Working knowledge of cGMP/QSR requirements and related documentation.

Responsibilities

• Assemble medical devices in a cleanroom per QSR/ISO13485 and SOPs.
• Perform in-process inspection to verify quality conformance.
• Record lot history data and maintain component accountability.
• Set up and operate manufacturing equipment.
• Maintain cleanroom standards and housekeeping per procedures.
• Report process or documentation issues and assist resolutions.
• Complete personal training records and maintain attendance onsite.

Skills

Basic math skills

English proficiency

Effective communication

Attention to detail

Manual dexterity

cGMP/QSR knowledge

Education

High School or equivalent with 1+ year clean room experience

Tools

Microscope

Soldering iron

Tweezers

Job description

Penumbra, Inc. in Salt Lake City, UT, is seeking a Production Builder I to assemble medical devices in a cleanroom environment on the day shift. Under supervision, you will perform moderately complex assembly, data recording and basic product testing, following QSR/ISO13485 and company SOPs.

Your responsibilities include set-up of manufacturing equipment, in-process inspection, maintaining cleanliness, and ensuring accurate lot records, with training completed and on-site attendance required.