Job Description. Objective / Purpose. The Senior Manager Clinical Data Management is responsible for timely and high quality data management deliverables supporting the Takeda portfolio. They are responsible for conducting oversight of Data Management activities at the project or program level - as performed within Takeda or by Strategic Partners, CROs or other 3rd Party Vendors - to ensure they meet obligations as described in ICH-GCP and Takeda...
Job Description. Associate Director, Access Marketing, Entyvio. Takeda Pharmaceutical. Lexington, MA. About the role. Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine. Join us as the Associate Director, Access Marketing, Entyvio. This position reports into the Director, Access and Life Cycle Management Marketing, Entyvio and is a part of the GI Business Unit. How you will contribute. ...
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 Pharmaceuticals America, Inc. for the following job opportunity. JOB LOCATION: Lexington, MA. POSITION: Senior Project Manager. POSITION DESCRIPTION: Takeda Pharmaceuticals America, Inc. is seeking a Senior Project Manager with the following duties: Perform Strategic Planning and Implementat...
Lead Manufacturing Technician. The. Takeda Lead Manufacturing Technician. is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations. This role will fully participate in both departmental projects and quality working teams. Under the general direction of the supervisor, this position shall be responsible for the hands-on execution of all ac...
Manufacturing Technician III. This role reports to a Manufacturing Supervisor and involves executing all processes in production while following cGMP, environmental health and safety guidelines. Key Responsibilities. Requirements. Working Conditions.
Job Description. About the role. As the Head of Compliance and Systems you will ensure compliance with all applicable provisions of the Takeda Quality Management System, and the regulations and standards applicable to Thousand Oaks operations. You will conduct gap analyses, implementing Quality Management System procedures across several departments, and managing compliance. You will interface with regulators during inspections, oversees Quality ...
Job Description. OBJECTIVES/PURPOSE. Build a centralized team within GCSC that is responsible for facilitating and supporting Ancillary supply process across the portfolio Responsible for enhancing and optimizing existing processes, defining new processes, and developing strategies to facilitate and support the delivery of ancillary supplies to support program and study needs including sourcing strategy, inventory management, kit assembly, packag...
Job Description. 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. The medical/scientific director will provide scientific & team leadership, guidance acr...
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description. OBJECTIVES/PURPOSE. The Head of ICSS Business Engagement and Demand Management is a ...
Job Description. About the role. The Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the quality of processes and product outputs. This role involves defining and specifying activities, processes, and standards to meet quality requirements, auditing and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high-quality standards, this role supports Takeda's mis...
Job Description. About the role. The Associate Director, Head of IG Purification Manufacturing is responsible for leading a multi-shift, 24/7 operation team to manufacture the final IG product before filling operations. This role ensures the efficient and compliant production of goods, aligning with Takeda's mission to bring better health to people and a brighter future to the world. How you will contribute. Lead a cross functional manufacturing ...
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that. the information I provide in my application will be processed in line with. Takeda’s. Privacy Notice. and. Terms of Use. I further attest that all information I submit in my employment application. is. true to the best of my knowledge. Job Description. Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an applica...
