Assembler I

AssemblerLocation: Pomona, CA, 91767 Duration: 12 Months of Contract + possible extension Shift: Monday to Friday (6:00 AM to 2:30 PM)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 housekeepingPerforms 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 equipmentMay be tasked with the completion and accuracy of documentation associated with the manufactured product and equipment maintenanceMay be tasked with cleaning, performing and documenting routine equipment maintenance and minor repairDisposes 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 validationMay be required to assist with problem-solving related to product qualityAbility to read and comprehend basic instructions and other work related documents.Demonstrate strong customer service skills while maintaining product QualityParticipate in root cause analysis and implement corrective actions under the guidance of Supervisor or ManagerCollaborates with Engineers, Maintenance Technicians, QC Technicians and Management to identify and help implement process improvementsWorks on assignments that are semi-routine in nature where judgment is required in resolving problems and making routine recommendationsUnderstands 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 activitiesResponsible 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 relationshipsCarries out duties in compliance with established business policiesOther duties as assigned, according to the changing needs of the businessMINIMUM QUALIFICATIONS | EDUCATION/EXPERIENCE:High school diploma or GED2-5 years related experienceBasic communication and written skillsAssignments require limited judgement in troubleshooting proven processes.Will perform job in a quality system environmentPREFERRED QUALIFICATIONS:3 years' experience preferable in medical device manufacturingMS Office Suite experienceKnowledge of regulations (FDA, ISO, OSHA, etc.)Basic understanding of manufacturing systems (documentation, compliance, inventory control, production scheduling/ controls, etc.)