We are seeking a Senior Mechanical Engineer to support the development and lifecycle management of disposable fluid-path components within our Urology portfolio. This role will focus on injection-molded plastic components and assemblies including cartridges cassettes tubing systems connectors sealing interfaces locking mechanisms and other flow-control components integrated into electromechanical medical devices.
The engineer will divide their time between sustaining existing products and supporting the development of new tubing and disposable solutions. The role places particular emphasis on supplier collaboration product lifecycle ownership injection-molded plastic design and the resolution of design manufacturing and field-related issues.
You will serve as a primary technical interface with suppliers while partnering with an experienced plastics subject matter expert and cross-functional teams in Quality Manufacturing Advanced Operations Supplier Quality and Sourcing. This team structure provides strong technical mentorship and support while allowing the engineer to build ownership of assigned components and projects.
What You Will Do
Translate customer and product needs into engineering requirements specifications and mechanical designs for disposable fluid-path components.
Support the design and development of cartridges cassettes tubing systems connectors sealing interfaces locking mechanisms and other plastic components.
Create and evaluate design concepts through prototyping engineering analysis and proof-of-concept testing.
Develop 3D models engineering drawings tolerance analyses and GD&T documentation.
Apply injection-molding design principles including material selection part geometry dimensional requirements tooling considerations and manufacturing feasibility.
Lead technical collaboration with suppliers during concept development design reviews tooling development component qualification and production support.
Evaluate supplier capabilities and work with Supplier Quality and Sourcing to address quality cost delivery and manufacturability requirements.
Review supplier-proposed concepts and provide technical recommendations based on product performance design requirements and manufacturing risk.
Plan execute analyze and document design verification testing.
Support design transfer engineering builds process validation and the introduction of new or modified components into production.
Investigate product manufacturing and field issues using structured root-cause analysis and corrective-action methods.
Identify opportunities to improve product reliability manufacturability quality and cost.
Maintain design documentation and contribute to design controls risk-management activities and the Design History File.
Communicate technical decisions risks recommendations and project status to internal stakeholders and external suppliers.
Minimum Qualifications
Bachelors degree in Mechanical Engineering Biomedical Engineering or a related engineering discipline is required
Two or more years of product-development experience is required.
Experience designing injection-molded plastic parts or small plastic components is required
.
Preferred Qualifications
Understanding of plastic-material selection manufacturing processes and injection-molding design principles.
Experience creating 3D models and engineering drawings using GD&T.
Experience with tolerance analysis design verification testing and root-cause investigation.
Knowledge of mechanical engineering principles including mechanics of materials component design and manufacturing processes.
Ability to communicate technical information clearly and collaborate with internal teams and external suppliers.
Experience with disposable medical products fluid-path components tubing systems connectors seals or flow-control mechanisms.
Experience working directly with suppliers on component design tooling manufacturability qualification or quality improvement.
Experience supporting both new product development and sustaining or lifecycle engineering.
Familiarity with supplier quality processes PPAP process validation or production-part qualification.
Experience applying statistics design of experiments or systematic problem-solving methods.
Experience developing products within a regulated industry.
Familiarity with medical-device design controls risk management FDA requirements or ISO 13485.
Experience supporting field investigations customer complaints nonconformances or corrective and preventive actions.
$101000 - $168400 USD Annual
Travel Percentage: 10%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: Hybrid or OnsiteIts Time to Join Stryker!We are seeking a Senior Mechanical Engineer to support the development and lifecycle management of disposable fluid-path components within our Urology portfolio. This role will focus on injection-molded plastic components and assemblies incl...
Work Flexibility: Hybrid or Onsite
Its Time to Join Stryker!
We are seeking a Senior Mechanical Engineer to support the development and lifecycle management of disposable fluid-path components within our Urology portfolio. This role will focus on injection-molded plastic components and assemblies including cartridges cassettes tubing systems connectors sealing interfaces locking mechanisms and other flow-control components integrated into electromechanical medical devices.
The engineer will divide their time between sustaining existing products and supporting the development of new tubing and disposable solutions. The role places particular emphasis on supplier collaboration product lifecycle ownership injection-molded plastic design and the resolution of design manufacturing and field-related issues.
You will serve as a primary technical interface with suppliers while partnering with an experienced plastics subject matter expert and cross-functional teams in Quality Manufacturing Advanced Operations Supplier Quality and Sourcing. This team structure provides strong technical mentorship and support while allowing the engineer to build ownership of assigned components and projects.
What You Will Do
Translate customer and product needs into engineering requirements specifications and mechanical designs for disposable fluid-path components.
Support the design and development of cartridges cassettes tubing systems connectors sealing interfaces locking mechanisms and other plastic components.
Create and evaluate design concepts through prototyping engineering analysis and proof-of-concept testing.
Develop 3D models engineering drawings tolerance analyses and GD&T documentation.
Apply injection-molding design principles including material selection part geometry dimensional requirements tooling considerations and manufacturing feasibility.
Lead technical collaboration with suppliers during concept development design reviews tooling development component qualification and production support.
Evaluate supplier capabilities and work with Supplier Quality and Sourcing to address quality cost delivery and manufacturability requirements.
Review supplier-proposed concepts and provide technical recommendations based on product performance design requirements and manufacturing risk.
Plan execute analyze and document design verification testing.
Support design transfer engineering builds process validation and the introduction of new or modified components into production.
Investigate product manufacturing and field issues using structured root-cause analysis and corrective-action methods.
Identify opportunities to improve product reliability manufacturability quality and cost.
Maintain design documentation and contribute to design controls risk-management activities and the Design History File.
Communicate technical decisions risks recommendations and project status to internal stakeholders and external suppliers.
Minimum Qualifications
Bachelors degree in Mechanical Engineering Biomedical Engineering or a related engineering discipline is required
Two or more years of product-development experience is required.
Experience designing injection-molded plastic parts or small plastic components is required
.
Preferred Qualifications
Understanding of plastic-material selection manufacturing processes and injection-molding design principles.
Experience creating 3D models and engineering drawings using GD&T.
Experience with tolerance analysis design verification testing and root-cause investigation.
Knowledge of mechanical engineering principles including mechanics of materials component design and manufacturing processes.
Ability to communicate technical information clearly and collaborate with internal teams and external suppliers.
Experience with disposable medical products fluid-path components tubing systems connectors seals or flow-control mechanisms.
Experience working directly with suppliers on component design tooling manufacturability qualification or quality improvement.
Experience supporting both new product development and sustaining or lifecycle engineering.
Familiarity with supplier quality processes PPAP process validation or production-part qualification.
Experience applying statistics design of experiments or systematic problem-solving methods.
Experience developing products within a regulated industry.
Familiarity with medical-device design controls risk management FDA requirements or ISO 13485.
Experience supporting field investigations customer complaints nonconformances or corrective and preventive actions.
$101000 - $168400 USD Annual
Travel Percentage: 10%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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