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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!

Summary/Objective:

Responsible for leading Supply Chain, Production, and Production Engineering to achieve safety, quality, delivery, cost, and compliance objectives. Provides strategic and technical leadership for manufacturing scale-up, operational excellence, continuous improvement, and new product introduction within a regulated medical device environment.

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]

• Directs Supply Chain, Production, and Production Engineering activities in accordance with quality system procedures.
• Leads daily manufacturing operations to ensure products are produced safely, efficiently, on schedule, and in compliance with applicable requirements.
• Develops and executes operational plans to improve quality, throughput, capacity, inventory, and cost performance.
• Provides engineering leadership for manufacturing process development, equipment selection, automation, process validation, and continuous improvement.
• Partners with Design Engineering, Quality, Regulatory, and Program Management to support new product introduction, design transfer, and manufacturing scale-up.
• Oversees production planning, material availability, inventory management, supplier performance, and supply continuity.
• Establishes and monitors key performance indicators for safety, quality, delivery, productivity, inventory, and cost.
• Develops departmental budgets, staffing plans, capital expenditure justifications, and resource recommendations.
• Leads investigations and implementation of corrective and preventive actions related to manufacturing and supplier issues.
• Ensures manufacturing processes remain validated and compliant with applicable medical device regulations, standards, and internal procedures.
• Develops organizational capability through hiring, coaching, performance management, and succession planning.
• Supports internal, customer, and regulatory audits and ensures timely completion of Operations-related corrective actions.
• Establishes and maintains Standard Operating Procedures, work instructions, and forms related to areas of responsibility.
• Works in accordance with quality system procedures.
• Other duties as assigned by Supervisor.

Required Education and Experience

• Bachelor's degree in Mechanical, Manufacturing, Electrical Engineering, or a related engineering discipline.
• Minimum of ten (10) years of progressively responsible experience in medical device manufacturing or operations.
• Minimum of five (5) years of leadership experience managing manufacturing operations, supply chain, and/or engineering teams.
• Demonstrated experience with manufacturing engineering, production operations, supply chain management, and quality systems.
• Experience with process validation, equipment qualification, manufacturing scale-up, and design transfer.
• Experience managing budgets, capital projects, resource plans, and operational performance metrics.

Preferred Experience and Qualifications

• Experience leading operations in a Class II or Class III medical device environment.
• Working knowledge of FDA Quality System Regulation, ISO 13485, and applicable international medical device requirements.
• Experience with ERP and Manufacturing Execution Systems.
• Experience implementing automation, Lean Manufacturing, Six Sigma, and structured continuous improvement methods.
• Strong analytical and problem-solving skills with the ability to make data-driven decisions.
• Excellent communication skills, including the ability to influence cross-functional teams and represent Operations to internal and external audiences.
• Proven ability to build, develop, and lead high-performing teams.
• Ability to manage multiple priorities in a fast-paced, highly regulated manufacturing environment.

Work Environment and Personal Protective Equipment

• This job operates in a professional office environment; many of the job's duties may be performed remotely. This role routinely uses standard office equipment such as computers, phones, photocopiers, and scanners. Personal Protective Equipment may be required for laboratory or field work.

Physical Demands

• While performing the duties of this job, the incumbent is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with co-workers.
• This position requires up to twenty percent (20%) travel. Some of the travel is international.

Location

• This position is based out of our office in Irvine, California.

Salary Range

$170,000 - $230,000

Benefits

• Comprehensive medical and dental coverage
• FSA and HSA Plan Options, including an annual company contribution to the HSA
• 401(k) program with employer match
• Generous vacation accrual and paid holiday schedule

Equal Employment Opportunity Statement

It is the policy of Beta Bionics to provide equal employment opportunity to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Beta Bionics will provide reasonable accommodations for qualified individuals with disabilities.