Assembler I

Position Details Position: Assembler I Location: Pomona, CA Duration: 12 months Shift: 6 AM - 2:30 PM Pay rate: $20.00/hr Very detailed work. Will use Masterflex – set it up and give volume to fill. Follow guidelines 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. Phone interviews will be conducted before offers. 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. Required Skills 2-5 years of experience in assembling, filling, and packaging reagents. No blueprint experience needed. Pharma experience ideal but not required. Packaging experience and ability to read work orders are necessary. Food environment experience also acceptable. Minimal Excel and basic computer skills. Most documentation is printed and written (not digital). Responsibilities May be tasked with completing set-up operations for assembly, packaging, and prep in compliance with approved documentation and QSR. This includes line clearance, equipment preventive maintenance, and housekeeping. Performs routine tasks working from detailed written or verbal instructions. Assembles, repairs, inspects, and/or tests products following written instructions. Assists Engineering and Maintenance teams with troubleshooting, maintenance, and repair of equipment. May be tasked with completion and accuracy of documentation related to the manufactured product and equipment maintenance. May be tasked with cleaning, performing, and documenting routine equipment maintenance and minor repair. Disposes hazardous waste material in the corresponding hazardous waste areas. Supports continuous improvement activities (e.g., 5S and OEE). Supports 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. Demonstrates strong customer service skills while maintaining product quality. Participates in root cause analysis and implements corrective actions under 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 that may occur from 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 company policies and practices; builds productive internal/external working relationships. Carries out duties in compliance with established business policies. Other duties as assigned, according to changing needs of the business. Minimum Qualifications High school diploma or GED. 2-5 years of related experience. Basic communication and written skills. Assignments require limited judgment in troubleshooting proven processes. Will perform job in a quality system environment. Preferred Qualifications Three 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.). #J-18808-Ljbffr Creative Solutions Services, LLC