We're sorry, the job you are looking for at Teva on EuroPharmaJobs has expired.
Click here to see more jobs at Teva .
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
This role is responsible for the day‑to‑day management and execution of key quality assurance activities related to the manufacture of commercial and investigational medicinal products. Core responsibilities include oversight of quality systems,
You will be responsible for managing the required quality activities and documentation associated with the portfolio of CMOs, ensuring that the CMOs manufacture and deliver products in compliance with Sanofi’s requirements specifications and regulations
Ensure that all NPI and Commercial Products manufactured at AbbVie Biologics are in accordance with the relevant GMPs. Ownership and Accountability for the Management and oversight for effective product transfer of NPIs and transfer to commercial
Lead and ensure compliance of global CQA processes across multiple sites; Act as key Quality partner for cross-functional stakeholders (e.g. Clinical Trial Teams, Biometry, CROs); Drive continuous improvement initiatives and proactively identify risks and
The role is responsible for formulation design and process development across various modalities, with a focus on ADCs, within the Formulation Technology Research Laboratories (FTRL). Responsibilities include supporting the preparation of regulatory