Senior Engineer, Mechanical Test

Cork - Ireland

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

Work Flexibility: Onsite

Permanent hybrid role based in #carrigtwohill Cork

Responsibilities

Prepare specifications for product safety and performance testing with a high degree of complexity (i.e. creation of test plans and complex test protocols). Typical products may be additive manufactured arthroplasty and trauma products as well as instruments required for implantation.
Project planning of product safety and performance tests and test campaigns.
Execute product safety and performance tests including documentation in test reports and approval thereof.
Analyze and assess results gained utilizing adequate analytical and statistical means and methods according to pre-existing guidelines.
Analyze and calculate loads (forces and moments) acting in the human body as input to simulations and calculations of implant loading as well as for adequate layout mechanical test set-ups.
Manage external test projects (i. e. sterilizations validations cleaning validations biocompatibility testing electromagnetic testing).
Communicate discuss and conclude test and analysis results in cooperation with product development teams
Consult development Engineers in biomechanical questions.
Prepare and create new guidelines (standard operating procedures).
Communicate on best practices and methodologies and share those across sites with subject matter experts from other sites.
Oversee subject matter expertise related to international standardization (ISO ASTM FDA guidance others) and implement requirements into guidelines.
Functionally lead the work of technicians specialists and project engineers in the field of Biomechanics.

Requirements

Bachelors Degree in Engineering or related
Minimum of 2-3 years of relevant experience in the medical device industry or equivalent.
Demonstrated ability to successfully contribute to complex ver/val test campaigns and lead less complex test campaigns.
Demonstrated ability to apply lab related design controls within a regulated industry.
Demonstrated knowledge and ability to apply fundamental and some advanced concepts practices and procedures of practical field of specialization.

Travel Percentage: 10%

Required Experience:

Senior IC

Work Flexibility: OnsitePermanent hybrid role based in #carrigtwohill CorkResponsibilitiesPrepare specifications for product safety and performance testing with a high degree of complexity (i.e. creation of test plans and complex test protocols). Typical products may be additive manufactured arthrop...

Work Flexibility: Onsite

Permanent hybrid role based in #carrigtwohill Cork

Responsibilities

Prepare specifications for product safety and performance testing with a high degree of complexity (i.e. creation of test plans and complex test protocols). Typical products may be additive manufactured arthroplasty and trauma products as well as instruments required for implantation.
Project planning of product safety and performance tests and test campaigns.
Execute product safety and performance tests including documentation in test reports and approval thereof.
Analyze and assess results gained utilizing adequate analytical and statistical means and methods according to pre-existing guidelines.
Analyze and calculate loads (forces and moments) acting in the human body as input to simulations and calculations of implant loading as well as for adequate layout mechanical test set-ups.
Manage external test projects (i. e. sterilizations validations cleaning validations biocompatibility testing electromagnetic testing).
Communicate discuss and conclude test and analysis results in cooperation with product development teams
Consult development Engineers in biomechanical questions.
Prepare and create new guidelines (standard operating procedures).
Communicate on best practices and methodologies and share those across sites with subject matter experts from other sites.
Oversee subject matter expertise related to international standardization (ISO ASTM FDA guidance others) and implement requirements into guidelines.
Functionally lead the work of technicians specialists and project engineers in the field of Biomechanics.

Requirements

Bachelors Degree in Engineering or related
Minimum of 2-3 years of relevant experience in the medical device industry or equivalent.
Demonstrated ability to successfully contribute to complex ver/val test campaigns and lead less complex test campaigns.
Demonstrated ability to apply lab related design controls within a regulated industry.
Demonstrated knowledge and ability to apply fundamental and some advanced concepts practices and procedures of practical field of specialization.

Travel Percentage: 10%

Required Experience:

Senior IC

Key Skills

Continuous Integration
Jenkins
Test Cases
Performance Testing
C/C++
LabView
Jira
Software Testing
System Testing
Test Automation
Selenium
Cerner

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About Company

Stryker

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongsid ... View more

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