Assembler II - Weekend Swing Shift

Essential Duties and Responsibilities

• [Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Qualified candidates who need a reasonable accommodation with the application process and/or to perform the essential functions of the position should notify the company’s HR contact]
• Support company goals and objectives, policies and procedures, Good Manufacturing Practices, and FDA regulations including compliance to EN ISO 13485, Medical Device Quality Standards.
• Comply with company Standard Operating Procedures (SOPs) and departmental policies and procedures (DOPs), objectives, the quality assurance program, as well as safety and environmental standards. Ability to establish, build and maintain professional working relationships with all levels of staff, clients, and suppliers.
• Ability to work with minimal supervision.
• Excellent interpersonal, verbal, and written communication skills. Meticulous attention to detail and meeting deadlines.
• Ability to learn new equipment and processes, and quickly demonstrate proficiency in their operation.
• Read and interpret manufacturing procedures, engineering drawings, and inspection procedures and comply with their requirements. All documents are written in English.
• Demonstrates accuracy, thoroughness and monitors own work to ensure quality.
• Practice and advocate good safety skills at all times.

Required Education, Experience, and Skills

• High School Diploma preferred.
• Preferred 3+ years related industry experience in medical device production assembly.
• 3+ years of experience in a medical device environment preferred.
• Experience in FDA/GMP/ISO environment preferred.

Required Skills

• Ability to apply principles outlined in Quality System Regulations (QSRs/GMPs).
• Ability to use basic hand tools such as hand tools, micrometers, calipers, etc.
• Ability to operate electrical and mechanical equipment and interpret results.
• Ability to work well with others in a cross-functional team environment.
• Attention to detail to ensure high quality work and to detect when there are issues with tooling, materials, processes and quality.
• Read, interpret, and learn engineering drawings, manufacturing procedures and processes and inspection procedures.
• Ability to work on a computer with various programs to transact product within the production system and complete online training.
• Ability to communicate clearly both verbally and in writing and ability to demonstrate active listening.

Location & Position Details

• This position is based out of our office in Irvine, California 92618
• Contract to Hire

Pay Rate

Hours

Work Environment

Physical Demands

Equal Employment Opportunity Statement