Position Overview

Ceribell is currently seeking a Manufacturing Supervisor. We are looking for a highly motivated individual who thrives in a fast-paced work environment. The Manufacturing Supervisor oversees production operations, ensuring manufacturing processes run reliably and efficiently. This position requires close collaboration with various teams, including Production Planning, Engineering, and Quality Assurance.

What You'll Do

• Supervise daily production line operations while adhering to regulatory standards, i.e. CFR 21; ISO 13485.
• Collaborate with the Production Planner for manufacturing schedule alignment and workflow optimization.
• Perform work order transactions in the ERP system, ensuring accuracy and timely execution.
• Address and resolve equipment malfunctions and production delays promptly.
• Lead, train, and mentor manufacturing staff, promoting a continuous improvement culture.
• Enforce safety guidelines and protocols to maintain a safe working environment.
• Work with the Quality Assurance team to swiftly address quality concerns.
• Participate in the Material Review Board (MRB) process, dealing with non-conforming materials and products.

• Participate in the RMA process, dealing with return and refurbishment of products.
• Collect and report data on product failure and root causes during production activities.
• Stay up-to-date of industry best practices related to the production line.
• Assist in managing and maintaining essential company assets for daily operations.
• Monitor and report on production metrics, pinpointing areas for improvement.
• Engage with Engineering, Logistics, and Inventory teams to refine processes and assist in developing assembly instructions, test methods, and reports for new product introductions.

What You'll Need

• Bachelor’s degree in Engineering, Manufacturing, Production Management, or equivalent experience.
• 5+ years in medical device production, with a preference for experience with capital equipment and disposables.
• 3+ years in a leadership or supervisory role within manufacturing.
• Familiarity with MRB processes and NCR procedures.
• Familiarity with ECO processes.
• Experience in New Product Introductions (NPI).
• Experience in Internal, ISO audit.
• Experience in production planning and scaling.
• Familiar with NetSuite ERP or similar systems.
• Solid understanding of regulatory standards such as CFR 21, ISO 13485, and GMP.
• Proficient with basic applications (Excel, Word, Outlook) and Quality Management Systems (QMS), including associated software like Arena.
• Strong communication, interpersonal, and problem-solving skills.
• Ability to lead effectively and adapt in a fast-paced environment.
• Familiarity with both semi and fully-automated medical device assembly technologies.
• Experience with electronics and electrical test equipment is a plus.

This job description is not intended to be all-inclusive. Employees may perform other related duties as negotiated to meet the ongoing needs of the organization.

Note: Candidates must be legally authorized to work in the United States.