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.

We are seeking a strong QA professional to assist in the development, implementation and maintenance of QA systems. We are currently in Phase III clinical trials (a first for the company) and need to add to the team a growing knowledge of GxP regulations and someone who can contribute to the development of Standard Operating Procedures and other quality related documents in preparation for bringing our lead product to market. In addition we need someone to actively participate in external, internal and vendor audits.

We are looking for candidates that embrace our core values of Integrity, Innovation, Collaboration, Compassion, Commitment and Excellence. We ask that you have a BA/BS preferably in a scientific discipline and 3+ years relevant QA experience. We also need demonstrated technical proficiency, a firm knowledge of quality systems and regulations, and an understanding and capability to trend and evaluate data. Experience with related CMC activities for license submission, Pre-Approval Inspections (PAI) and electronic quality system tracking systems are a plus. If you are adept at learning software systems then this is the position for you.

For full immediate consideration, interested, qualified candidates are encouraged to email their resume (attached Word document please) and cover letter to:

[email protected]
Therion Biologics Corporation
Human Resources
76 Rogers Street
Cambridge, MA 02142
Fax: (617) 475-7249

For more information on Therion please go to our website at www.therionbio.com

Therion is an equal opportunity employer.