Are you looking for a patient-focused, innovation-driven company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda.
Join us as our Quality Specialist Disposition. Our Disposition team is accountable for batch disposition for Biologics product manufactured at CMOs on behalf of Takeda.
The scope includes Drug Substance, Drug product and Finished Drug Product The Disposition team will work with our external CMO partners and internal Quality teams.
In addition, this function works closely with External Supply, Supply Planning, Technical support and any stakeholders involved in external supply.
Key Accountabilities Reviewing batch documentation, data, certificates of analyses, technical reports and providing support to Quality Disposition personnel Evaluating, designing and implementing quality systems relating to batch disposition Maintaining and improving quality metrics that incorporate continuous improvement methodologies Facilitating, approving and providing inputs into deviation investigations, change controls, CAPA, investigations and nonconformance reviews as required Supporting batch disposition processes as required person will work in collaboration with the Disposition team, Quality teams and cross functionally with external supply, planning, technical and other stakeholders including CMO partners to disposition batches.
Evaluation of CMO’s Quality Management Systems to ensure appropriate level and content of reporting, including technical evaluation of quality system reports Evaluation of batch manufacturing records to determine assurances of safety, identity, strength, quality, or purity Determining impact of production / release schedule changes to commercial supply On-
going evaluation of Takeda’s batch review / release systems to ensure efficient and effective processes are implemented with integrated continuous improvement methodologies You will lead continuous improvement initiatives in the batch disposition team and support continuous improvement initiatives in Biologics external supply The scope of this role spans Drug Substance, Drug Product, Finished Drug Product manufactured at multiple CMOs across the region Key skills required Thorough understanding of quality systems and cGMPs.
Manufacturing site experience would be valuable. Experience conducting audits and / or involvement in preparation for Health Authority inspections.
Education, Behavioural Competencies 6 years’ + experience working in manufacturing and / or Quality to support the manufacturing of biologic products.
Strong technical / Quality background with specific experience in Biologics manufacture. Manufacturing site experience would be valuable.
Interpersonal skills and communication skills to interact with CMO partners and other functions. Must be able to prioritize in a busy environment.
Must be available to travel -approx 20% (domestic and international) Notice to Employment / Recruitment Agents : Employment / Recruitment agents may only submit candidates for vacancies only if they have written authorization to do so from Shire, a wholly-
owned subsidiary of Takeda’s Talent Acquisition department. Any agency candidate submission may only be submitted to positions opened to the agency through the specific Agency Portal.
Shire, a wholly-owned subsidiary of Takeda will only pay a fee for candidates submitted or presented where there is a fully executed contract in place between the Employment / Recruitment agents and Shire, a wholly-
owned subsidiary of Takeda and only if the candidate is submitted via the Agency Portal. Candidates submitted or presented by Employment / Recruitment Agents without a fully executed contract or submitted through this site shall not be deemed to form part of any Engagement for which the Agency may claim remuneration.