CAD Designer, Equipment & Automation - 1st shift

Abbott•Madison, WI

2d•Hybrid

About The Position

Our Mission at Abbott Cancer Diagnosics is to eradicate cancer and the suffering it causes – through tests that help prevent it, detection that finds it earlier, and guidance for its successful treatment. Come join our team and make a difference in other people’s lives. The CAD Designer, Equipment and Automation, will create Solidworks models, assemblies, and drawing files to support new products and equipment launches, as well as changes to existing equipment and products. This is an on-site role with some flexibility to work remotely. This position will maintain the PLM Vault system, ensuring parts and assemblies are up to date and documented correctly in the Quality and Manufacturing systems. This position supports a collaborative environment that promotes positive teamwork where all members are working for the good of Exact Sciences. This is an ideal role for a hands-on Mechanical Designer with good communication skills looking to make an impact on the fight against cancer.

Requirements

Associate’s degree in CAD or related field with 8 years of experience using Solidworks; or, in lieu of Associate’s degree, a minimum of 10 years of experience using Solidworks.
Minimum of 8 years of experience of designing parts for machining, forming, and molding manufacturing operations.
Minimum of 8 years of experience creating assemblies, managing part revisions, and providing documentation for assembly operations.
Possesses extensive knowledge of engineering design, manufacturing practices, and procedures, and applies this knowledge to complete assignments.
Authorization to work in the United States without sponsorship.
Demonstrated ability to perform the Essential Duties of the position with or without accommodation.

Nice To Haves

Previous experience with metal and plastic fabrication, including machining, sheet metal and 3D printing.
Experience using Solidworks Electrical, Simulation, and Finite Element Analysis (FEA) tools.
Experience working in manufacturing or engineering environments, applying problem solving skills and process improvements.
Experience in engineering or relevant life sciences / medical device industry.
Experience working in an FDA/cGMP/CAP/CLIA regulated production environment.

Responsibilities

Create new part and assembly designs that meet internal stakeholder requirements and are cost effective to produce with external manufacturing partners.
Utilize extensive knowledge of design tolerances, material properties, and various manufacturing processes to ensure optimal designs for business needs.
Facilitate design review meetings with stakeholders to seek feedback, assess needs, and convert requests to completed work.
Create Assembly files with complete Bill of Materials to support manufacturing operations.
Create Drawing files using correct tolerances, including GD&T, materials of construction, applicable notes, and maintain revision history.
Check, mark-up, and approve drawings for release.
Use computer assisted design/drafting software to develop, design, manage, and maintain drawings.
Develop, maintain, and oversee the PDM Vault database following best practices for drawing creation and lifecycle management.
Mentor CAD software users on best practices for drawing management.
Train drawing users on the available drawing resources including how to access, read, request corrections, and request creation of new drawings.
Update and maintain templates and engineering standards for Solidworks.
Assist in continuous improvement initiatives.
Obtain quotes from vendors and order parts as needed.
Create documentation of design files for GMP requirements.
Document and submit First Article Inspection Reports and non-conformance investigations as needed.
Create assembly documentation for the manufacturing and quality systems in accordance with FDA, GMP, ISO, CAP, CLIA requirements.
Apply technical knowledge of internal operations, external manufacturing processes, and/or material properties to enhance company products and equipment.
Prepare and present written and oral reports.
Follow procedures and maintain detailed records.
Manage time and competing priorities.
Ability to work independently and as part of a team.
Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
Support and comply with the company’s Quality Management System policies and procedures.
Regular and reliable attendance.
Occasional evening and weekend work may be required.
Ability to lift up to 50 pounds for < 5% of a typical working day.
Ability to work seated for approximately 80% of a typical working day.
Ability to work standing for approximately 20% of a typical working day.
Ability to work in front of a computer screen and/or perform typing for approximately 80% of a typical working day.
Ability to comply with all applicable personal protective equipment requirements.
Ability to travel approximately 10% of working time for occasional training, out of state vendor site visits, and travel between Exact Sciences sites.
Other duties as assigned.