JOIN OUR TEAM

DESCRIPTION

• Cutting edge product development work

• Product design of medical devices

• Responsible for the mechanical design, development, and drafting/drawing needs for products from

• Early-stage concept development into production including fixtures and equipment needed to support the product

• Provide support with broad range of prototype initiatives

• Responsible for engineering documentation

• Successfully contributes to project team including the following activities: design and engineering, design

• Change strategy, test of materials, preparation of specifications, process capability studies, research

• Investigations, report preparation and test documentation.

• Assistance in working on high visibility/high business importance projects

• Works cross-functionally with project management, quality, manufacturing, regulatory, clinical and marketing to ensure project success

REQUIRED

• Must be located in greater Twin Cities area, no relocation funds available for this role

• Self-Starter with the ability to work independently / with a team to plan, schedule and execute activities necessary to meet project timelines.

• Medical Device industry experience preferred.

• Proficient in 3D modeling and reasoning.

• Tolerance analysis experience

• Able to prepare standard reports/documentation to communicate results to technical community

• Ability to work within a regulated industry environment and with a track record of accomplishments

• Experience with standard engineering test method design and execution

• Summarizes, analyzes, draws conclusions, and provides recommendations from test results

• Effective communication skills required due to support of cross functional projects within a team

• Can work independently to plan and schedule own activities necessary to meet timelines

• Able to lead design change to ensure the proposed changes are systematically and thoroughly analyzed to verify that the design intent is still met

PREFERRED

• Very proficient in SolidWorks

• GD&T experience

• ePDM / Agile / Enovia experience

• Fundamental understanding of design controls and risk management within the medical device industry

• Fundamental understanding of the Quality System per ISO 1348 5 or 21 CFR820

• Electro-mechanical development experience

Job type: Full-time

Benefits:

• 401(k)

• 401(k) matching

• Dental insurance

• Health insurance

• Health savings account

• Paid time off

• Professional development assistance

• Referral program

• Tuition reimbursement

• Vision insurance

Schedule:

• 8 hour shift

• Monday to Friday

Education:

• Bachelor's (Preferred)

Experience:

• Medical device: 0-2 years (Preferred)

Work Location: In-person

DESCRIPTION

• Cutting edge product development work

• Product design of medical devices

• Responsible for the mechanical design, development, and drafting/drawing needs for products from

• Early-stage concept development into production including fixtures and equipment needed to support the product

• Provide support with broad range of prototype initiatives

• Responsible for engineering documentation

• Successfully contributes to project team including the following activities: design and engineering, design

• Change strategy, test of materials, preparation of specifications, process capability studies, research

• Investigations, report preparation and test documentation.

• Assistance in working on high visibility/high business importance projects

• Works cross-functionally with project management, quality, manufacturing, regulatory, clinical and marketing to ensure project success

REQUIRED

• Must be located in greater Twin Cities area, no relocation funds available for this role

• Self-Starter with the ability to work independently / with a team to plan, schedule and execute activities necessary to meet project timelines.

• Medical Device industry experience preferred.

• Proficient in 3D modeling and reasoning.

• Tolerance analysis experience

• Able to prepare standard reports/documentation to communicate results to technical community

• Ability to work within a regulated industry environment and with a track record of accomplishments

• Experience with standard engineering test method design and execution

• Summarizes, analyzes, draws conclusions, and provides recommendations from test results

• Effective communication skills required due to support of cross functional projects within a team

• Can work independently to plan and schedule own activities necessary to meet timelines

• Able to lead design change to ensure the proposed changes are systematically and thoroughly analyzed to verify that the design intent is still met

PREFERRED

• Very proficient in SolidWorks

• GD&T experience

• ePDM / Agile / Enovia experience

• Fundamental understanding of design controls and risk management within the medical device industry

• Fundamental understanding of the Quality System per ISO 1348 5 or 21 CFR820

• Electro-mechanical development experience

Job type: Full-time

Benefits:

• 401(k)

• 401(k) matching

• Dental insurance

• Health insurance

• Health savings account

• Paid time off

• Professional development assistance

• Referral program

• Tuition reimbursement

• Vision insurance

Schedule:

• 8 hour shift

• Monday to Friday

Education:

• Bachelor's (Preferred)

Experience:

• Medical device: 2-5 years (Preferred)

Work Location: In-person

DESCRIPTION

• Cutting edge product development work

• Product design of medical devices, including catheters, delivery systems and capital equipment

• Responsible for the mechanical design, development, and drafting/drawing needs for products from early-stage concept development into production including fixtures and equipment needed to support the product

• Provide support with broad range of prototype initiatives

• Responsible for engineering documentation

• Successfully contributes to project team including the following activities: design and engineering, design change strategy, test of materials, preparation of specifications, process capability studies, research investigations, report preparation and test documentation.

• Assistance in working on high visibility/high business importance projects

• Works cross-functionally with project management, quality, manufacturing, regulatory, clinical and marketing to ensure project success

REQUIRED

• Self-Starter with the ability to work independently / with a team to plan, schedule and execute activities necessary to meet project timelines.

• Proficient in 3D modeling and reasoning.

• Tolerance analysis experience

• Able to prepare standard reports/documentation to communicate results to technical community

• Ability to work within a regulated industry environment and with a track record of accomplishments

• Experience with standard engineering test method design and execution

• Summarizes, analyzes, draws conclusions, and provides recommendations from test results

• Effective communication skills required due to support of cross functional projects within a team

• Can work independently to plan and schedule own activities necessary to meet timelines

• Able to lead design change to ensure the proposed changes are systematically and thoroughly analyzed to verify that the design intent is still met

PREFERRED

• Catheter design experience

• Very proficient in SolidWorks

• GD&T experience

• ePDM / Agile / Enovia experience

• Fundamental understanding of design controls and risk management within the medical device industry

• Fundamental understanding of the Quality System per ISO 1348 5 or 21 CFR820

• Electro-mechanical development experience

Job Type: Full-time

Benefits:

• 401(k)

• 401(k) matching

• Dental insurance

• Health insurance

• Health savings account

• Paid time off

• Professional development assistance

• Referral program

• Tuition reimbursement

• Vision insurance

RESPONSIBILITIES

• Adhere to the Quality Management System and documented processes

• Ensure communication and documentation between engineering, production and quality is clear, consistent and current.

• Assist with development and implementation of inspection procedures

• Ensure robust inspection procedures

• First Article/ Start-up Inspections

• Work In Process Inspections

• Perform sampling inspections

• Assist in training personnel on how to perform In Process inspections and ensure that all training is documented per procedure

• Operate and program CMM, Micro-Vu, and Keyence inspection equipment

• Communicate all adjustments to inspection priorities

• Adhere to the manufacturing schedule to ensure priority processing

• Provide input for the refinement of all inspection processes

• Assist with calibration as requested

• Assist with updating and creating In Process (IP) inspection sheets

REQUIRED QUALIFICATIONS AND SKILLS

Technical Skills

• Programming Machine Vision Systems

• Quality Inspection Experience

• Basic math required

• Knowledge of GD&T and/or inspection methods

• Able to read and understand blueprints

• Able to accurately use inspection equipment

• Working technical knowledge in the use of height gages, profilometer, comparator, and hand tools (calipers, micrometers, bore gages, etc…)

Computer Skills

• Microsoft Office software (Word, Excel, and Outlook)

• Enterprise Resource Planning (ERP) software

EDUCATION AND EXPERIENCE

• Associate’s degree, vocational training, or equivalent training and experience required

• Technical training in the utilization of inspections methods and equipment required

• Experience and implementation of Statistical Process Control (SPC)

• Minimum 5 years experience in Quality Systems in an ISO regulated manufacturing environment preferred (custom medical device contract manufacturing preferred)

MACHINES AND TECHNOLOGIES

• CAM Software

• Calipers and Micrometers

• Vision System (Keyence)

• Coordinate Measuring Machine (CMM)

Job type: Full-time

Benefits:

• 401(k) matching

• Dental insurance

• Employee assistance program

• Flexible spending account

• Health insurance

• Health savings account

• Life insurance

• Paid time off

• Referral program

• Tuition reimbursement

• Vision insurance

Experience level:

• 5 years

Schedule:

• 8 hour shift

• Monday to Friday

DESCRIPTION

• Programming of parts while holding tight tolerances

• Experience in programming high precision parts

• Quick turn prototypes highly desirable

• Setup of complex milling machines

• Read and interpret customer supplied prints, internal work instructions and job processing travelers

• In-Process inspection of parts and monitoring of processes to ensure parts follow Lucid’s workmanship standards and exceed customer expectations

• Multitasking a must with the ability to work on numerous projects while maintaining quality standards

• Ability to work well in a team environment and independently to complete and meet production goals

• Quick change over skills highly desirable

• Manage full programs from prints to completion

• Able to work with others and help with manufacturing processes and problem solving

• Familiar with tool setters and part probing is a plus

• GD&T skills and knowledge of G&M codes

• Ability to keep and maintain a clean and safe workplace is a must

• Identify opportunities for improvement and act if appropriate before a problem occurs

• Other duties as required within an agile work environment

SHIFT / HOURS

• 1st shift / 2nd shift – flexible

• Full-time: 40 hours per week plus overtime if desired

BENEFITS

• 401(k) / 401(k) matching

• Health insurance, dental insurance, vision insurance, Health Savings Account (HSA)

• Flexible schedule

• Paid time off

• Professional development assistance

• Referral program

• Retirement plan

• Tuition reimbursement

• Team environment

Do you have what it takes to join our team? Please email us your resume.