Medical Device Assembler (1st Shift) - $20/HR!! DN2025

Job Title: Assembler I
Location (On-site, Remote, or Hybrid?): Pomona, CA (onsite)
Contract Duration: Contract until 10/26/2026
Working hours: 6:00am - 2:30pm
Total hours: 40

Description:

The position of Assembler I is within our CMI business unit located in California. Under general supervision, the scope of this position is responsible for setting up and performing adjustments to equipment used in support of manufacturing. Ability to diagnose and perform routine technical troubleshooting is required.

This job description will be reviewed periodically and is subject to change by management.

RESPONSIBILITIES:
May be tasked with completing set-up operations for one of the following: assembly, packaging and prep operations in compliance with approved documentation, and QSR. This will include but not limited to line clearance, equipment preventative maintenance and housekeeping
Performs routine tasks working from detailed written or verbal instructions.
Assembles, repairs, inspect and/or test products following written instructions.
Assist the Engineering and Maintenance teams with trouble shooting, maintenance, and repair of equipment
May be tasked with the completion and accuracy of documentation associated with the manufactured product and equipment maintenance
May be tasked with cleaning, performing and documenting routine equipment maintenance and minor repair
Disposes hazardous waste material on corresponding hazardous waste areas.
Required to support continuous improvements activities, (e.g. 5S and OEE, etc.)
Support new equipment installation and validation
May be required to assist with problem-solving related to product quality
Ability to read and comprehend basic instructions and other work related documents.
Demonstrate strong customer service skills while maintaining product Quality
Participate in root cause analysis and implement corrective actions under the guidance of Supervisor or Manager
Collaborates with Engineers, Maintenance Technicians, QC Technicians and Management to identify and help implement process improvements
Works on assignments that are semi-routine in nature where judgment is required in resolving problems and making routine recommendations
Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities
Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices; build productive internal/external working relationships
Carries out duties in compliance with established business policies
Other duties as assigned, according to the changing needs of the business

MINIMUM QUALIFICATIONS | EDUCATION/EXPERIENCE:
high school diploma or GED
0-3 years related experience
Basic communication and written skills
Assignments require limited judgement in troubleshooting proven processes.
Will perform job in a quality system environment

PREFERRED QUALIFICATIONS:
3 years’ experience preferable in medical device manufacturing
MS Office Suite experience
Knowledge of regulations (FDA, ISO, OSHA, etc.)

Basic understanding of manufacturing systems (documentation, compliance, inventory control, production scheduling/ controls, etc)