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Takeda Pharmaceuticals Associate Director, Quality Risk Management in Lexington, Massachusetts

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Job Description

Shire Human Genetic Therapies, Inc. is seeking an Associate Director, Quality Risk Management in Lexington, MA with the following requirements: Bachelor’s degree in Biology, Chemistry, Mechanical Engineering, Chemical Engineering or related field or foreign academic equivalent plus 7 years of related experience. Prior experience must include: Design, develop and implement quality risk management process and tools utilizing technical writing skills; lead, facilitate and provide consultation on complex and technical risk assessments within the GxP domain; lead a global network of QRM practitioners to foster risk-based thinking/approach and share best practices and lessons learned; create risk assessment tools/templates to assess risks and implement software solutions (electronic workflows and dashboards) to effectively document, track and communicate risks; provide training on application of quality risk management principles and risk assessment tools such as FMEA, PHA, HACCP etc. Up to 20% travel required. Up to 40% telecommuting allowed; must live within normal commuting distance of Lexington, MA.

Apply on-line at and search for Req #R0097231.


EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.


Lexington, MA

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Time Type

Full time