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.
Responsible to supervise and lead the Laboratory release function including Raw Materials, Intermediates, DPI and API’s (including the stability program) and In Process Control and provide core technical support in areas of chromatography,
Responsible for developing and overseeing a robust Quality Assurance strategy focused on the transfer of New Product Introduction (NPI) QC methods to manufacturing sites and Third-Party Laboratories. This role supports the Test Method Gate Review process,
Develop, implement, and maintain the quality management system applicable to R&D activities (SOPs, work instructions, standards, etc.). Ensure compliance of R&D projects assigned to CMO Office with relevant regulations (e.g., GCP, GVP, GMP, GLP, ISO, ICH,
Are you an experienced manager and an inspirational leader seeking a new challenge within Quality? Do you want to make a meaningful impact in a company dedicated to advancing cancer diagnostics and improving patient outcomes? If so, we invite you to
Lead, plan, and coordinate daily cell and tissue culture activities in compliance with GMP standards. Supervise and mentor a team of (Senior) Biotech Associates, ensuring quality and efficiency in manufacturing. Initiate and follow up on deviations,