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Staff Engineer, Device Testing

Lexington, Massachusetts
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  • Job Level: Senior
  • Travel: Minimal (if any)

Takeda has been translating science into breakthrough medicines for 240 years. Every step of the way, our teams have worked together to tackle some of the most challenging problems in drug discovery and development. Today, we’re a driving force behind innovative therapies that make a lasting difference to millions of patients around the world.

In R&D, all of our history and potential comes together in an environment that welcomes diversity of thought and amplifies every voice. Working closely with colleagues, you’ll play a key role in bringing our rich pipeline of products forward to help patients. Come join a team that’s earned trust for more than two centuries, and find out how advancing transformative therapies at Takeda will shape your bright future.

Job ID R0152827 Date posted 05/23/2025 Location Lexington, Massachusetts

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Job Description

Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity:

JOB LOCATION: Lexington, MA

POSITION: Staff Engineer, Device Testing

POSITION DESCRIPTION: Takeda Development Center Americas, Inc. is seeking a Staff Engineer, Device Testing with the following duties: develop test methods and test method validation protocols and perform testing at the Device Design and Testing Lab; may help transfer test methods to external laboratories during all stages of combination product development; set up, operate, and validate test equipment and perform test method qualifications by following standard operating procedures; support overall test laboratory activities, including test development, gage R&R studies, coordination of stability studies and tests, calibration, and preventive maintenance of test equipment; provide input to the design of fixtures for new experiments, tooling, equipment, and specifications; establish and foster collaborative relationships with internal device and combination product development and quality teams as well as external test equipment development and testing partners and service providers; support investigations of out-of-spec test results and deviations; and participate and interact on project teams. Up to 5% domestic travel required.

REQUIREMENTS: Master’s degree in Mechanical Engineering, Materials Engineering, Biomedical Engineering, or related field, plus 2 years of related experience. Prior experience must include: analyze data to determine experimental significance and make recommendations for future steps based on this and develop methods for testing and characterizing devices and materials; assess applicability of new laboratory equipment and coordinate installation, calibration and maintenance; establish and foster collaborative relationships with internal teams as well as external vendors, consultants, testing partners and service providers; create medical device and laboratory documentation such as SOPs; manage projects including the preparation of timelines and scheduling and perform advanced statistical analysis including Design of Experiments and Gage R&R.

Full time. $111,800 to $191,600 per year. Competitive compensation and benefits.

Qualified applicants can apply at https://jobs.takeda.com. Please reference job #R0152827. EOE

Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.

Locations

Lexington, MA

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time
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During my 20-year journey here, I’ve been fully supported by my colleagues, and I can’t say enough about our rich internal talent and the long-standing values that drive our decisions as we work to develop important medicines for the patients we serve.

Doug Coffman - Head, R&D Asset Transition & Integration Office, R&D Regional & Business Operations

When making any type of decision, the first thing we ask is 'how will this impact patients?’ Ultimately, we’re laser focused on the best interests of the patient, and I truly believe we follow through on that.

Meredith Culp - VP, Head of Neuroscience Therapeutic Area Strategy & Operations and Head of Global Development Integration Office

Our culture and shared values make us like a family here at Takeda. It doesn't feel like work when you're doing something you love with people you love, and when your outcome is really fantastic.

Alison Handley, Head, Center for External Innovation

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Lexington, Massachusetts


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