Quality Compliance Manager

at  Takeda Pharmaceutical

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MORE ABOUT US:

Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and departments, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines.
Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and. Over the past two years, Takeda Ireland has invested over €55 million in Ireland to develop our manufacturing sites. Solidifying our commitment in our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years.

ABOUT THE ROLE:

This is a management position in an ethical Solid Oral Dosage Pharmaceutical Formulation
and Finished Product plant. The brief requires a thorough knowledge of Good Manufacturing
Practice, current FDA & EMEA regulations for solid oral dosage pharmaceuticals for human
use and a good working knowledge of manufacturing processes, packaging processes and
validation activities used in the pharmaceutical industry. Good organizational, supervisory,
technical writing and investigation skills are required.

General Responsibilities:

• Drive and promote the corporate values of Takeda-ism within the workplace.
• Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.
• Drive and maintain staff development.
• Drive and Maintain Department KPIs.
• Drive and support site must win battles.
• Other duties as required and directed by the Site Quality Head, or other Officer appointed by the Board of Directors