Specialist in Quality Assurance Disposition

1 settimana fa


Roma, Lazio, Italia Takeda Pharmaceutical A tempo pieno

About the Role: As a QA Disposition Specialist at Takeda Pharmaceutical, you will play a crucial role in ensuring the correct disposition of intermediates, guaranteeing their proper handling and processing. Your responsibilities will include verifying the accuracy and completeness of information necessary for further processing and final product release. You will also contribute to maintaining departmental KPIs within established targets.

Key Responsibilities:

Perform and support checks for product shipment and authorization for further processing, ensuring that product release occurs within applicable requirements and scheduled times.
Approve or reject preliminary checks for product disposition.
Perform and support activities related to product disposition, as per the release management procedure.
Contribute to maintaining departmental KPIs.
Support the management of trial batches.
Perform and support activities related to product holds, returns, BPDR, FCA, post-release, and PQR, as needed.
Review SOPs and specifications, as necessary.
Support the maintenance of the GMP archive for your department, including responsibility for managing obsolete document destruction.

Requirements:

Bachelor's degree in technical or scientific disciplines.
At least 4 years of experience in a similar position or analogous roles within the Quality Assurance field.
Ability to work in a team, positive attitude, and demonstration of behaviors aligned with Takeda's values.
Ability to influence others.
Good command of the English language.



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