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Shire Senior Device Development Engineer – Auto Injectors in Lexington, Massachusetts
Summary: The Senior Engineer will lead technical efforts for auto injector drug delivery device projects. As a hands-on technical contributor and device subject matter expert (SME), this person will provide project and engineering leadership in the concept, feasibility, development, qualification and launch phases of device development. Area of focus will include identification of user needs, specification development, prototyping, test development, design verification and validation testing, risk assessments, equipment development oversight. Extensive collaboration with internal and external partners.
Responsibilities (% of time): Provide technical leadership on cross functional teams for devices through clinical development, product registration and commercialization. Own and lead the creation of design control deliverables to comply with medical device and combination device regulations. – 50% Establish and maintain detailed project plans, define risks and recommend contingency plans as required. 20% Lead project execution activities and oversee the development of statistically sound design verification protocols/reports and design validation. – 20% Establish and foster strong collaborative relationships with external design/development, manufacturing partners and service providers. 5% Lead or assist in deviation, complaint and failure investigations. 5%
Requirements: More than 5 years’ experience in the field of medical device or combination product development and commercialization is required. Proven track record in developing auto injectors preferred. Prior technical leadership experience with creating design control/technical file deliverables and manufacturing scale-up a plus. A Bachelor’s of Science Degree in Engineering required, a Master’s of Science Degree preferred. Experience in developing and commercializing regulated devices / combination products under Design Control (21 CFR 820) and ISO14791 requirements. Proven track record of developing and gain regulatory approval of drug delivery systems a plus Knowledge of global industry standards (ex: ISO, AAMI, ANSI, etc..). Strong hands on technical leadership skills with a track record of delivering new products to market. Strong communication skills (written and verbal), including experience presenting in front of multidisciplinary audiences, is desirable. DFSS certification is highly desirable. Prior experience leading projects with external design, development and manufacturing partners. Working knowledge of solid works desirable.
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Equal Employment Opportunity
Shire, a wholly-owned subsidiary of Takeda, is an Equal Opportunity Employer committed to a diverse workforce. Shire, a wholly-owned subsidiary of Takeda, will not discriminate against any worker or job applicant on the basis of race, color, religion, gender, national origin, ancestry, age, sexual orientation, marital or civil partnership status, pregnancy, gender reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, application for military service, or membership in any other category protected under law.
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Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own.