Senior Associate (f/m/d) Gene Therapy

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The Position

-For this position, only applications from restructuring areas of the Legal Entity Roche Diagnostics will be considered at this time.-

Are you looking for a new challenge?

In Roche’s Pharmaceutical Cell & Gene Therapy organization (PTC), we are united by our vision to drive and realize cell and gene therapies by translating scientific progress into life-changing experiences for patients.

Our core business is to bring game-changing viral vector based therapies from early clinical supply into the market to serve patients with an unmet clinical need to cure diseases.

We are doing this by developing world-class AAV manufacturing processes using cutting-edge technology for the whole value chain.

Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to make extraordinary life-changing gene therapies a reality for the patients.

 

The position:

You will join an expert team in the area of clinical GMP manufacturing for viral vector based therapies.

The main objective of your work is to support GMP manufacturing processes for AAVs.

Additionally, you will be responsible for the introduction of new technologies and the qualification of new equipment in the production area.

You can expect a versatile and varied job in a highly innovative working environment.

 

Key responsibilities include, but are not limited to the following tasks:


* You are responsible for process equipment and devices for the clinical production of viral vector based therapies under GMP


* You perform purification of viral vectors under S2 conditions, preparation of solutions required in the GMP and any downstream activities yourself and supervise these processes.


* You perform commissioning and qualification of systems and devices you work with


* You create SOPs or other documents under GMP requirements


* You support the digitalization by active contribution to digital and data analytics projects

 

You can identify with the following statements?


* You have qualified scientific training and many years of professional experience in purification, ideally you have worked in the GMP area.


* They have extensive knowledge and practical experience in the purification of proteins on a scale of up to 2000 L under GMP conditions.


*  Your experience with single-use technologies up to 2000L scale will help you to accomplish the required tasks.


* You are experienced to work in a GMP environment and to deal with viral vectors including biosafety requirements


* You a...