Assembler

Eastridge Workforce Solutions

Work Environment

Works in a Lab, Clean Room, and Warehouse environment, within a well-lighted work area with good ventilation and normal noise levels from lab, shop equipment, and clean room.
Sitting or standing at a production workstation with frequent walking to transact products; intermittently write or use a keyboard to communicate through written means.

Summary/Objective

The Assembler will perform duties associated with electro-mechanical and clean room device assembly and packaging. The critical attributes and skills required for this position include manual hand assembly skills, attention to detail, initiative, working well within a team, and ability to produce consistently high-quality results.

Essential Duties and Responsibilities

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.
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 always advocate good safety skills.

Required Education, Experience, and Skills

High School Diploma preferred.
Preferred 2-5 years related industry experience in medical device production assembly.
2-5 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 products within the production system and complete online training.
Ability to communicate clearly both verbally and in writing and ability to demonstrate active
listening.

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Vacancy posted 2 days ago

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