Jobs · Engineering · California

Manufacturing Engineer II

Glaukos Corporation · San Clemente, CA · 2 wk ago
EngineeringFull-time

What You'll Do

  • Performs a variety of manufacturing engineering activities on ocular related products including manufacturing scale up, development, and sustaining activities.
  • Develops creative solutions to manufacturing problems, develops and executes process, equipment, and product validations, ensures the proper engineering deliverables are accurately generated, generates 3D CAD models and 2D CAD drawings for assembly tools and fixtures, test procedures, project management and leadership, and maintains schedule.
  • May lead manufacturing related project teams with other engineers, technicians, and manufacturing staff with a focus on meeting manufacturing requirements with technically strong, high quality, cost effective approaches.

How You’ll Get There

  • Experience: BS Mechanical Engineering or equivalent required, 2+ years of medical device or pharmaceutical experience, experience with ocular product a plus, detail oriented with the ability to work in a clean room environment, experience with phased new product development processes from concept through full production release, ability to work in team environment as contributor and leader, ability to create and maintain scheduled plans while maintaining quality of engineering deliverables with guidance for engineering management, excellent decision making/problem solving skills, strong verbal and written communication skills, proficient in MS Word, Excel, Statistical Software, Outlook, and MS Power Point, ability to use MS Project (for level Sr and Principal), 2+ years or experience working as manufacturing engineering on complex medical device / pharma subassembly and top-level assembly builds, 2+ years of experience working with a wide range of manufacturing methods, including machined, extruded, molded and laser cut parts, 2+ years’ experience generating tooling / fixturing design to support production, Solidworks design preferred, knowledge of cGMP and ISO regulations required, experience with MRP a plus, ability to interact with all departments required, ability to coordinate activities with outside vendors.

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