1. Internal projects: Develop analytic methods and execute analytic assays of AAV vectors for gene therapy process developments; Design, develop and execute bioassays of in vitro and in vivo samples to advance gene therapy projects.
2. External projects: Support tech transfer and on-going activities with external collaborators and service providers (CMOs, CROs).
3. Data presentation: Maintain accurate, timely and detailed records of work; Communicate and present findings in internal and external meetings.
4. Collaboration: Collaborate across the company to assure that timelines developed are adhered to by appropriate assignments of internal and external resources.

Basic Qualifications
Education Background: Ph.D. in biology, virology or a related field with 2 years industry experience, or M.S. with 5 years of industry experiences in developing analytic assays for AAV vectors, and in vitro assays for preclinical research applications.

Working Experience Requirement

1. Experience with viral vectors is required and previous management of CROs is a plus.
2. Prior experience in establishing analytical methods and conducting analytical assays suitable for viral vector characterization is required.
3. Prior experience in establishing conducting bioassays for preclinical in vitro and in vivo studies is required.
4. Experience with writing assay protocol, documentation and study reports that could contribute to regulatory filing documents is a plus.
5. Ability to work independently as well as being part of a team is essential; possess self-motivation, adaptability, and a positive attitude.
6. Ability to balance multiple projects under a demanding timeline while providing guidance to project teams.

1. Skilled in the development of molecular biology test methods, including PCR, ELISA, HTRF, SDS Page and cell based potency assays.
2. Hand on experiences with AAV analytics are required.
3. Excellent organizational, communication and collaborations skills are required.
4. Professional Training
5. Experience in authoring regulatory documents, including IND is a plus.