Formulation Process Engineer

* Take part in technology Transfer process for specific Taizhou products being transferred from

other Site to Taizhou site, on the formulation / process from technical perspective- Lead the

receiving site activities to enable successful TT these may include TORA, establishment trials,

validation manufacture, stability batch generation and documentation to support the process

* Be responsible to the cleaning validation procedure, and execution of miscellaneous cleaning

validation studies including Process equipment and Packaging equipment, if applicable

* Supportive to the equipment and clean utilities commissioning- as part of the project effort, it

may include process parameter setting up for wet granulation, tableting process until coating,

and completion of process validation until the success of the GMP inspection and license

* Ensure the regulatory/GMP compliance on the process/technical dossier, and relative

coordination work if required

* Also, as a receiving site, will take part in the assessment of NEW product feasibility of Taizhou

facility, and their manufacturability in Taizhou site and ensure products can be produced in

compliance with AZ quality standard and site Lean requirement

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.