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Balt

Engineering Manager - Operations

Reposted 22 Days Ago
Be an Early Applicant
In-Office
Irvine, CA
150K-170K Annually
Senior level
In-Office
Irvine, CA
150K-170K Annually
Senior level
The Engineering Manager oversees manufacturing engineers to enhance processes for medical devices, ensuring safety and quality while integrating new products into production. Responsibilities include management of a team, optimizing operations, and conducting process validation.
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About Balt  

Our purpose is to improve the lives of 150,000 patients in 2026.  

 Our story 

Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians and institutions to develop elegant medical devices.  Our products are being used by physicians across the world, and we have 13 offices in 11 countries – and counting. 

We introduced one of the first neurovascular intervention devices in 1977 and now offer the world's broadest portfolio of medical devices for stroke. As the premier global neurovascular platform always seeking to expand beyond boundaries, we are now bringing our innovation to the peripheral vascular space.

We are proud of our mission, our people, and the incredible work we accomplish together as we empower physicians to save lives. 

 Why Join Balt? Join a passionate team, dedicated to making a difference.  

  1. Working at Balt means giving meaning to your work! Pride is a strong part of our identity.  
  2. We are a close-knit team, with strong mission, vision and values that guide our day-to-day.  
  3. Recognition of work, respect, and our multicultural community are key aspects of the employee experience and contribute to our continued success.  
  4. No matter the country, we take care of you.  

Would you like to be part of our story? Don't hesitate, come and join us! 

 About this opportunity – Engineering Manager, Operations

Description

This fast-paced position will be primarily responsible for the management of manufacturing engineers. You will have the responsibility to support and continuously improve current manufacturing processes, through technical and process innovation for the manufacture of neurovascular medical devices that save patient lives.

 Job Responsibilities

  • Lead a team of Manufacturing Engineers and Technicians in supporting the ongoing manufacturing of commercial products as well as ensuring flawless integration of new products into the manufacturing environment.
  • Daily work includes leadership and execution in both sustaining and project work –complete the types of projects that remove the need for engineering intervention– improving safety, quality, output and cost.
  • Provide support to the Manufacturing organization to facilitate efficient operations within the production area, to optimize existing processes, and to ensure that production goals are met. Further, improve systems to monitor performance of equipment, machines and tools and correct equipment problems or process parameters that produce non-conforming products, low yields or product quality issues. Interface with Quality and Research and Development organizations to integrate new products or processes into the existing manufacturing area.
  • Process validation and verification work is frequently required – knowledge of Process Validation Plans, IQ, OQ, PQ, Software validation, test method validation, gage R&R, and a clear understanding of FDA’s QSR and cGMP and a good understanding in statistics.
  • Creation and maintenance of models for product cost and capacity to help prioritize engineering and production resources related to improvement projects.

 Qualification Requirements

  • Four-year technical degree required(Bachelor’s), preferably in Engineering.
  • Class II, IIb, or III Medical Device Experience
  • 5 years minimum as an Engineer or engineering leader in a related field with at least 1 year being in a leadership/management role.
  • Deep process validation knowledge in medical device or pharmaceutical experience is required.
  • Equipment Development and Qualification experience
  • Working knowledge of statistical analysis of various data types for the purpose of validation and process control/monitoring
  • Neurovascular experience is a plus
  • Strong background in metals, plastics, extrusion, and/or adhesives is highly desired.
  • Experience creating, reading, interpreting and updating technical drawings for tooling/fixturing/equipment as well as part/product applications
  • SolidWorks and Minitab proficiency are highly desired.
  • Microsoft Project and Microsoft Visio proficiency are highly desired.

Skills:

  • Ability to train and manage engineers and technicians in various procedures and skillsets needed to maintain and improve commercial manufacturing
  • Directing engineers who lead project teams tasked with manufacturing improvement projects, manufacturing transfers as well as successful transfers into manufacturing.
  • Ability to prepare project plans, budgets, specifications, and schedules for engineering resources and projects.
  • Experience with catheters, balloons, or stents device manufacturing processes and equipment.
  • Project Management using MS Project or similar tool
  • Knowledge of DFM analysis and techniques to partner with development teams to bring products from pilot manufacturing into commercial manufacturing.
  • Experience with process FMEA as well as Process Development, Process Characterization and Process Validation.
  • Application of statistical and analytical methods such as SPC, SQC, and DOE.
  • Use of root cause analysis tools and techniques too address problems (NCMRs/CAPAs) or identify potential opportunities.
  • Process background (development, capability, optimization, validation) within the medical device industry including Lean and Six Sigma toolsets to analyze and improve production lines and processes.
  • Development of manufacturing documentation (Manufacturing Procedures, Engineering Drawings, BOM, Work Orders).
  • Effectiveness with lab equipment, assembly tools and measurement devices
  • Ability to perform routine analysis of test results in relation to design specifications and test objectives.
  • Characterize and define equipment functional requirements and system capabilities.
  • Development and qualification of tooling/ equipment (IQ/ OQ/ PQ, support, design).
  • Proficiency in SolidWorks.
  • Knowledge of computer applications (i.e.: Microsoft Project, Word, Excel, PowerPoint, Windows, Visio, etc.) required.
  • Ability to create presentations and effectively communicate relevant information to various levels of individual contributors and management.
  • Comfortable working independently and cross-functionally as part of a team
  • Experience designing manufacturing line layouts using Lean methodologies

More information please go to www.baltgroup.com 

Please be aware of a current job offer scam perpetrated through the use of the internet. The scammers frequently misappropriate and use a company’s log and photos to give the appearance of legitimacy. The scam preys upon those seeking employment and uses false and fraudulent offers of employment with employers, such as Balt Inc to steal from the victims. Balt believes that one of the best ways to put a stop to this scam is to make sure you are aware of it. Balt’s job recruitment process involves live communication: in person, telephone, and/or video interviews in most cases. 


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Pay Range
$150,000$170,000 USD

Top Skills

Lean
Microsoft Project
Microsoft Visio
Minitab
Six Sigma
Solidworks
Statistical Analysis

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