At Therion we are driven by our mission to Extend and Improve the Lives of Cancer Patients through Immunotherapy. If you are interested in a fast-changing, dynamic environment in a biotechnology company that is pioneering novel immune therapies for cancer, then Therion is the right company for you.

The Manufacturing team is currently seeking a collaborative person to support the GMP manufacture of clinical grade vaccines and cross-train into drug substance and drug product manufacturing as necessary.

Primary responsibilities - all aspects of cGMP manufacture of clinical grade vaccines, including:

� Mammalian cell culture, purification, aseptic filling, reagent preparation.
� Required to work in and maintain clean room environment.
� Draft SOPs, deviations, investigations.
� Maintain cGMP compliance through accurate record keeping and precise adherence to SOPs and batch records.
� Excellent written and verbal communication skills to work cross-functionally with other teams.

We are looking for candidates that embrace our core values of Integrity, Innovation, Collaboration, Compassion, Commitment and Excellence. The successful candidates will have a minimum of an Associate�s degree and 1-5 years of related experience. A Bachelor�s degree is preferred. If you have strong organizational skills and the ability to work cross-functionally this is the position for you.