Assembler I - Weekend Night Shift (4th Shift)

Beta Bionics•Irvine, CA

2d•Onsite

About The Position

The Assembler I 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. Beta Bionics is a medical technology company dedicated to bringing innovative type 1 diabetes management solutions to the many, not the few. We are committed to bringing better access to better solutions – and a better life for those living with diabetes – with the world’s first bionic pancreas called the iLet. The iLet Bionic Pancreas is the first and only insulin delivery system that does not require carb counting, bolusing, correction factors, or pre-set basal rates. The only number needed to get started with the iLet Bionic Pancreas is a user’s weight – the iLet does the rest. The iLet lets users “Go Bionic” with their diabetes management. User must be carb aware. Successful candidates will be working with highly experienced colleagues, who are amongst the best in their fields. We have a mission-driven, passionate and collaborative culture where you will have a high degree of empowerment and opportunity to make a significant impact. This is a Contract to Hire position.

Requirements

Manual hand assembly skills
Attention to detail
Initiative
Ability to work well within a team
Ability to produce consistently high-quality results
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.
Demonstrates accuracy, thoroughness and monitors own work to ensure quality.

Nice To Haves

Experience in FDA/GMP/ISO environment preferred
2+ years of experience in a medical device environment preferred.

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.
Read and interpret manufacturing procedures, engineering drawings, and inspection procedures and comply with their requirements. All documents are written in English.
Practice and always advocate good safety skills.