LanceSoft Inc
Join our dynamic team in Mounds View, MN, where you will have the opportunity to contribute to the development and reliability of cutting‑edge products in a collaborative and innovative environment.
Must Have:
Bachelor’s degree in Engineering, Science, or a related technical discipline
Experience in Reliability Testing, Design Verification, and/or Test Method Validation
Strong written and verbal communication skills and ability to work cooperatively as part of a cross‑functional team
Nice to Have:
1-3 years of Medical Device industry experience
Familiarity with FDA 21 CFR Part 820, EU 217/745 (EU MDR)
Knowledge of standards: ISO 13485, ISO 14971, IEC 60601
Proficiency in Microsoft Office Applications (Word, Excel, Access, and PowerPoint) and Windows OS
Responsibilities: As a Reliability Engineer, your responsibilities will include:
Developing, coordinating, and conducting technical reliability studies and evaluations of engineering design concepts and design of experiments (DOE) constructs
Recommending design or test methods and statistical process control procedures for achieving required levels of product reliability
Completing risk analysis studies of new design and processes
Compiling and analyzing performance reports and process control statistics; investigating and analyzing relevant variables potentially affecting product and processes
Ensuring that corrective measures meet acceptable reliability standards
Analyzing preliminary plans and developing reliability engineering programs to achieve company, customer, and governmental agency reliability objectives
Proposing changes in design or formulation to improve system and/or process reliability as necessary
Additional Details:
This is an onsite position at the Mounds View site
Target years of experience: 1-3 years
Interviewing and hiring to start ASAP
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Must Have:
Bachelor’s degree in Engineering, Science, or a related technical discipline
Experience in Reliability Testing, Design Verification, and/or Test Method Validation
Strong written and verbal communication skills and ability to work cooperatively as part of a cross‑functional team
Nice to Have:
1-3 years of Medical Device industry experience
Familiarity with FDA 21 CFR Part 820, EU 217/745 (EU MDR)
Knowledge of standards: ISO 13485, ISO 14971, IEC 60601
Proficiency in Microsoft Office Applications (Word, Excel, Access, and PowerPoint) and Windows OS
Responsibilities: As a Reliability Engineer, your responsibilities will include:
Developing, coordinating, and conducting technical reliability studies and evaluations of engineering design concepts and design of experiments (DOE) constructs
Recommending design or test methods and statistical process control procedures for achieving required levels of product reliability
Completing risk analysis studies of new design and processes
Compiling and analyzing performance reports and process control statistics; investigating and analyzing relevant variables potentially affecting product and processes
Ensuring that corrective measures meet acceptable reliability standards
Analyzing preliminary plans and developing reliability engineering programs to achieve company, customer, and governmental agency reliability objectives
Proposing changes in design or formulation to improve system and/or process reliability as necessary
Additional Details:
This is an onsite position at the Mounds View site
Target years of experience: 1-3 years
Interviewing and hiring to start ASAP
#J-18808-Ljbffr