Senior Supplier Process Engineer

2 weeks ago


Battle Creek, Michigan, United States Stryker Full time

Work Flexibility:
Hybrid


Stryker is seeking a Senior Supplier Process Engineer to enhance new product introductions within the Medical Division.


Who we seek:

Collaborative team players:

Individuals who cultivate and utilize cross-functional relationships to amalgamate ideas, data, and insights, driving ongoing enhancements across various functions.


Analytical thinkers:

Professionals who delve deeper than mere problem-solving to pinpoint root causes, assess optimal solutions, and propose comprehensive improvements to avert future challenges.

Self-motivated innovators:

Individuals who take initiative in their responsibilities and require minimal prompting to boost productivity, instigate change, and achieve results.


We are looking for a Senior Supplier Process Engineer to join the Advanced Operations team, focusing on the Acute Care Business Unit, primarily dedicated to launching innovative products that enhance patient support and the patient environment.

In this role, you will engage in the design transfer of new products from the research phase through development and into production.

This position offers a hybrid work environment.

Key Responsibilities:


Provide engineering support for new product and process introductions, ensuring compliance with Stryker's design transfer protocols.

Participate in PFMEA, Control Plan, SOP, and PPAP documentation related to new product launches.

Guarantee the quality of processes and products as outlined in the relevant operational and material specifications.

Assist in selecting components and equipment based on a thorough analysis of specifications, reliability, and regulatory criteria.

Support capital acquisition efforts, including equipment selection, procurement, installation, and validation.

Analyze equipment to establish operational data, conduct experimental tests, and analyze results.

Engage in process review meetings.

Develop inspection and testing method protocols/equipment.

Conduct MSA studies for new products and processes.


Be proficient in and mentor others on industry standards, including design requirements, manufacturing, and testing strategies in accordance with applicable regulations.


Collaborate effectively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management to ensure project success as a key team leader.

Deliver high-quality outcomes with enthusiasm, energy, and determination to meet business objectives.

Foster relationships and influence across engineering teams within the organization.

Qualifications:
Bachelor's degree in Engineering or a related technical field is required.

A minimum of 6+ years of relevant experience is required.

Ability to read and interpret complex engineering drawings and understand geometrical dimensioning and tolerancing is essential.

Familiarity with electrical components and manufacturing processes, including common failure modes, is required.

Proficiency in CAD and/or other design and analysis tools is necessary.

Capability to interpret and analyze system drawings with basic Mechanical/Software/Electrical interactions is required.

Experience in electronics circuit board and/or electro-mechanical system manufacturing is preferred.

Ability to interpret, analyze, and test electrical designs is preferred.

Experience in an FDA-regulated or similar industry is preferred.

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.

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