Manufacturing Engineering Technician I – Weekend Day Shift (3rd Shift)

Beta Bionics, Inc.•Irvine, CA

13d•Onsite

About The Position

Beta Bionics, Inc. 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. Please contact us if you fit the profile below and if you are interested in joining the Beta Bionics team! The overall responsibility for this role is ensuring reliable operation of production equipment through troubleshooting, maintenance, repair, calibration, and technical support. This role collaborates with Production, Engineering, and other departments to minimize downtime, improve processes, and support new product introduction while maintaining regulatory compliance, quality standards, customer satisfaction, and budget requirements.

Requirements

Experience in manufacturing industry, medical device preferred.
Ability to apply principles outlined in Quality System Regulations (QSRs/GMPs).
Ability to use basic hand tools such as drills, micrometers, calipers, etc.
Ability to operate electrical and mechanical equipment and interpret results
Must be able to read and interpret mechanical drawings and electrical schematics.
High School Diploma required.
1–3 years of manufacturing experience, preferably in the medical device or other regulated industries.
Experience with FDA, ISO 13485, GMP or similar quality systems is preferred.

Nice To Haves

Associate degree in a technical field is preferred

Responsibilities

Troubleshoot, maintain, repair, calibrate, and rework production equipment and assemblies to ensure reliable operation and minimize downtime.
Maintain and track accurate records of equipment maintenance, repairs, calibrations, inspections, and troubleshooting activities.
Collaborate with engineers and cross-functional teams to resolve equipment and process issues, implement improvements, and support new product introduction.
Maintain thorough knowledge of production processes, equipment, work instructions, and quality requirements.
Provide technical support to production lines, including equipment issues, changeovers, and production interruptions.
Perform root cause analysis and implement solutions to prevent recurring equipment, process, and production issues.
Work independently, prioritize assignments, and make timely decisions based on technical knowledge, analysis, and sound judgment. Ability to work with minimal supervision.
Manage multiple projects and technical activities while meeting deadlines and adapting to changing priorities.
Communicate effectively and maintain professional relationships with employees, clients, vendors, and suppliers.
Complete work accurately and thoroughly while maintaining strong attention to detail, safety, and quality.
Follow company policies, GMP, FDA regulations, EN ISO 13485 requirements, approved procedures, and applicable quality and safety standards.