Assembler I Pomona, CA

Assembler I Pomona, CA

Shift: 06:00 AM - 02:30 PM

Pay: 20/hr

Description:

Very detailed work.

Will use master flex- set it up and give volume to fill. Have a guideline to reference.

Lots of paperwork- basic knowledge of GMP, filling and packaging reagents

Basic math

Lifting no more than 15 lbs

On feet all day- Rotating through tasks throughout the day.

Required skills:

2-5 yrs Assembling, filling and packaging reagents experience. No blueprints experience needed.

Someone for pharma would be ideal but not required. As long as they have some packaging experience and can read work orders.

Food environment experience also acceptable

Software skills- minimal excel, basic computer skills

Most documentation is printed out and written (not digital)

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.

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 companys 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 Qualification:

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

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.)