This role focuses on product sustainment continuous improvement design changes and lifecycle management providing the opportunity to apply engineering expertise across manufacturing quality regulatory and testing functions. You will play a key role in maintaining product performance supporting technical investigations and implementing engineering solutions throughout the product lifecycle.
Work Flexibility: Hybrid: candidates must reside within commuting distance of Mahwah NJ and be able to work onsite several days per week.
What You Will Do
Represent the R&D sustainment engineering team at the manufacturing site and coordinate technical activities with global engineering and manufacturing partners.
Support product remediation maintenance and lifecycle management activities around customized implants within the CMF product portfolio.
Lead the evaluation development and implementation of engineering and design changes through established change management processes.
Develop and implement engineering solutions that enhance product performance manufacturability reliability and ongoing product support.
Assess the impact of design changes on product performance quality requirements manufacturing processes and regulatory compliance.
Conduct technical investigations of customer complaints nonconformities and product-related issues using structured root cause analysis methodologies.
Define document and implement corrective and preventive actions to address identified issues and support product reliability.
Create review and maintain engineering documentation technical specifications risk management files and design change records in compliance with applicable requirements.
What You Will Need
Required Qualifications
Bachelors degree in Engineering or related discipline.
Minimum 2 years of engineering experience.
Experience conducting technical investigations and root cause analyses.
Experience creating reviewing and maintaining engineering documentation and design change records.
Preferred Qualifications
Experience working in the medical device industry.
Experience implementing product changes within a regulated quality management system.
Experience collaborating with Quality Manufacturing Regulatory Affairs or Testing functions.
German language proficiency.
$93200 - $155400 USD Annual
Travel Percentage: 20%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant. However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge (b) in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer or (c) consistent with the contractors legal duty to furnish information.
Required Experience:
Senior IC
Work Flexibility: HybridSenior Engineer Research & Development Mahwah NJThis role focuses on product sustainment continuous improvement design changes and lifecycle management providing the opportunity to apply engineering expertise across manufacturing quality regulatory and testing functions. You ...
Work Flexibility: Hybrid
Senior Engineer Research & Development
Mahwah NJ
This role focuses on product sustainment continuous improvement design changes and lifecycle management providing the opportunity to apply engineering expertise across manufacturing quality regulatory and testing functions. You will play a key role in maintaining product performance supporting technical investigations and implementing engineering solutions throughout the product lifecycle.
Work Flexibility: Hybrid: candidates must reside within commuting distance of Mahwah NJ and be able to work onsite several days per week.
What You Will Do
Represent the R&D sustainment engineering team at the manufacturing site and coordinate technical activities with global engineering and manufacturing partners.
Support product remediation maintenance and lifecycle management activities around customized implants within the CMF product portfolio.
Lead the evaluation development and implementation of engineering and design changes through established change management processes.
Develop and implement engineering solutions that enhance product performance manufacturability reliability and ongoing product support.
Assess the impact of design changes on product performance quality requirements manufacturing processes and regulatory compliance.
Conduct technical investigations of customer complaints nonconformities and product-related issues using structured root cause analysis methodologies.
Define document and implement corrective and preventive actions to address identified issues and support product reliability.
Create review and maintain engineering documentation technical specifications risk management files and design change records in compliance with applicable requirements.
What You Will Need
Required Qualifications
Bachelors degree in Engineering or related discipline.
Minimum 2 years of engineering experience.
Experience conducting technical investigations and root cause analyses.
Experience creating reviewing and maintaining engineering documentation and design change records.
Preferred Qualifications
Experience working in the medical device industry.
Experience implementing product changes within a regulated quality management system.
Experience collaborating with Quality Manufacturing Regulatory Affairs or Testing functions.
German language proficiency.
$93200 - $155400 USD Annual
Travel Percentage: 20%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant. However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge (b) in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer or (c) consistent with the contractors legal duty to furnish information.
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
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