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 Objective / Purpose: The Quality Assurance Validation (QAV) Specialist provides independent quality oversight and guidance for validation, qualification and technical transfer activities at a GMP-regulated pharmaceutical manufacturing site. The role ensures that activities are appropriately planned, risk assessed, documented and approved, and that the resulting processes, equipment, facilities, utilities and systems are suitable for their intended use and remain in a validated state. The postholder works closely with Manufacturing, Quality Control, Engineering, Technical Operations, Regulatory Affairs and external partners to support compliant and timely project delivery. Key responsibilities •Provide QAV oversight for technology and technical transfers of products, processes, analytical methods and manufacturing knowledge into or between GMP sites. •Review and approve transfer plans, protocols, risk assessments, acceptance criteria, reports and associated change controls. •Assess transfer readiness, including gaps in process knowledge, facilities, equipment, utilities, analytical methods, documentation, training and material supply. •Provide QAV oversight for process validation and verification activities, including process performance qualification (PPQ), continued process verification and lifecycle management. •Review and approve validation protocols and reports, ensuring that the scientific rationale, sampling plans, acceptance criteria, deviations and conclusions are clear and supported by evidence. Locations Grange Castle, Ireland Base Salary Range: €57,800.00 - €79,420.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. For information about our benefits, please click here. Worker Type Employee Worker Sub-Type Fixed Term (Fixed Term) Time Type Full time Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own. Takeda is an equal opportunity employer. For applicants of U.S and Puerto Rico positions: Click here to learn about our commitment to Equal Employment Opportunity (EEO). If you are limited in the ability to use our job application tool, or otherwise require a reasonable accommodation for a disability please click here.

Quality Assurance Validation Executive.

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