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Job Description

Shire Human Genetic Therapies, Inc. is seeking a Senior Process Validation Engineer II in Lexington, MA with the following requirements: Master's degree in Pharmaceutical Manufacturing, Bioprocess Engineering, Chemistry, Biochemistry or related field or foreign academic equivalent plus 5 years of experience. Prior experience must include: Perform validation of processes and qualification of equipment for Biologics manufacturing operations; independently determine validation requirements applying risk assessment principles and industry standards; generate, plan, execute and document validation studies per regulatory guidelines; author content for regulatory submissions to support Biologics licenses.

Apply on-line at www.takedajobs.com and search for Req # R0088034.

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.

Locations

Lexington, MA

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time