Engineering Manager-Medical Device Tustin, CA

Trelleborg is a world leader in engineered polymer solutions for almost every industry on the planet. And we are where we are because our talents brought us here. By specializing in the polymer engineering that makes innovation and application possible, Trelleborg works closely with leading industry brands to accelerate their performance, drive their business forward—and along the way, shape the industry and progress that will benefit humankind in the exciting years ahead.

Location

Tustin/CA

Trelleborg Sealing Solutions US-Tustin, CA, is part of Trelleborg’s Healthcare and Medical Segment, we provide innovative quality medical device assembly and packaging, as well as engineering services and combination products to our customers. We are a USA ISO 13485-2016 certified company, with all services performed in California. Currently, there is an opportunity in our Engineering Department, for a Engineering Manager.

TSS is an Equal Opportunity Employer and offers an excellent benefits package that includes:
• Life Insurance
• Health Insurance
• Vision Insurance
• Dental Insurance
• 401(k) plan

The Engineering Manager is responsible for working closely with Sales and customers to develop competitive production processes for new opportunities. This role oversees a team of individual contributors to ensure departmental goals are established and achieved. 

Responsibilities include:

  • Organize and appropriately staff department 
  • Work with direct reports to communicate and update goals and/or metrics, illustrating objective evidence of improvement 
  • Determine feasibility of manufacturing and automation of new products in a competitive market 
  • Direct, review and approve new product development processes and necessary capital equipment 
  • Research and analyze new technologies 
  • Provide cross functional support to the overall organization 
  • Build customer relationships 
  • Follow ISO and site Quality Systems protocols 
  • Develop continuous improvement initiatives 
  • Support inter-departmental Goals and Objectives 

Qualifications: 

  • 4 Year degree in Engineering or equivalent 
  • 10+ years of engineering experience  
  • Experience in medical device or related industry 
  • 5 years of experience leading a team 
  • Knowledge of Validation processes, Control Plans, and FMEA’s 

Desired: 

  • Master’s degree with concentration in Polymer Science 
  • Experience with medical silicone and/or component manufacturing 

We welcome you to join our team during this exciting time!

Apply using this link:  https://bit.ly/3bhJTrN