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Maintenance engineer

Ospedaletto (Provincia di Treviso)
TAKEDA PHARMACEUTICALS AMERICA, INC.
Pubblicato il 12 settembre
Descrizione

Join to apply for the Maintenance Engineer role at TAKEDA PHARMACEUTICALS AMERICA, INC.

3 weeks ago Be among the first 25 applicants

Join to apply for the Maintenance Engineer role at TAKEDA PHARMACEUTICALS AMERICA, INC.

Skills

On the Global Manufacturing and Supply (GMS) team at Takeda, you’ll be part of a rapidly transforming industry that’s applying technology and data in new ways. Within our agile, innovative, people-centric organization, your work will matter every day as you use your skills to help us manufacture therapies for patients on our four platforms:

* Small Molecules
* Biologics
* Plasma
* Cell and Gene

As part of the GMS team, you'll have the opportunity to pursue unique experiences and build new skills, and you'll know that the work you do every day makes an impact — on our patients, our people, our planet, and on yourself.

Job ID R | Date posted 08/27/2025 | Location Pisa, Italy

Since 1972, Takeda has had two sites in Italy for producing plasma-derived drugs in Rieti and Pisa, supporting patients with rare and complex diseases. These sites focus on the production of therapies derived from immunoglobulins, albumin, and coagulation factors. We transform plasma into life-saving drugs under the “National Self-Sufficiency of Blood and its Products” program. We provide high-quality drugs worldwide, with a strong presence in Europe, America, and Asia.

Join us to make a difference.

About The Role

As a Maintenance Engineer, you will draft and manage maintenance contracts, organize and coordinate activities of external contractors, and ensure the performance and efficiency of the Maintenance Department and pharmaceutical equipment, aiming for operational excellence.

Responsibilities include:

1. Planning and scheduling corrective and preventive work orders according to CMMS and production schedules.
2. Supporting troubleshooting and maintenance activities in compliance with EHS and GMP rules for GxP/non-GxP equipment.
3. Managing parts, documentation, archives, and SOP reviews.
4. Drafting and managing maintenance contracts and coordinating related activities.
5. Ensuring compliance with EHS regulations and supporting safety culture.
6. Supporting shift information

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