Senior Engineer, Process Development

Work Flexibility : Hybrid

Stryker is one of the world’s leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care.

The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives.

We are currently seeking a Senior Engineer , Process Development to join our Instruments Division to be based in Portage, MI.

Who we want :

Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.

Dedicated achievers. Relentless about quality, people who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.

Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.

What you will do :

As the Senior Engineer, Process Development - Advanced Operations you will provide hands on engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures.

Ensure quality of process and product as defined in the appropriate operation and material specifications

Select components and equipment based on analysis of specifications, reliability and regulatory requirements

Work with quality engineers to develop component specific testing and inspection protocols

May lead or support capital acquisition activity from specifying equipment, contract negotiation, installation and validation

Analyze equipment to establish operating data, conduct experimental test and result analysis.

Lead and / or participate in process review meetings

Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches

Complete capability studies for in process inspection and generate subsequent Inspection documentation

Conduct MSA studies for new products and new processes

Use the latest engineering techniques to reduce product time to market whilst adhering to regulatory requirements, project deadlines and product costs

Build productive internal and external working relationships and may periodically provide guidance and train other team members

Provide training for manufacturing team members

Ensure adherence to GMP and safety procedures

Review and approval of validation documentation

What You Need :

Bachelor’s Degree in Engineering

2+ years of relevant post-grad work experience

Preferred Skills :

Knowledge of manufacturing processes, materials, product and process design

Ability to read and interpret complex engineering drawings

Electrical / Mechanical Engineering degree

Experience in a FDA regulated or highly regulated industry

Understanding of Design for Manufacturing (DFM), related statistical tools and validation / verification techniques

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 contractor’s legal duty to furnish information.