Glaukos
Glaukos
Posted 3 months ago
Full Time
Burlington, Massachusetts
In Person
Smart Summary
Responsibilities
Perform manufacturing engineering activities for ocular products, including scale-up, development, and sustaining activities. Responsibilities include creating CAD models, executing process validations, and leading project teams to meet quality and cost requirements.
Qualifications
You have experience in manufacturing scale-up, development, and sustaining activities for ocular related products. You are capable of developing creative solutions to manufacturing problems, executing process and product validations, and generating 3D CAD models and 2D CAD drawings.
Must Have Skills for ATS
3D CAD
2D CAD
process validation
product validation
project management
ISO 13485
21 CFR 820
Job Description
Performs a variety of manufacturing engineering activities on ocular related products including manufacturing scale up, development, and sustaining activities. Responsibilities include developing creative solutions to manufacturing problems, development and execution of process, equipment, and product validations, ensuring the proper engineering deliverables are accurately generated, generation of 3D CAD models and 2D CAD drawings for assembly tools and fixtures, test procedures, project management and leadership, and maintaining 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. Duties shall be performed with attention to detail while supporting Glaukos' Quality Policy and the appropriated regulatory agencies, including FDA Quality System Regulations (21 CFR 820) and ISO Standards (ISO 13485).
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