Associate Director, Purification Process Development
4 weeks ago
Vaxart Inc. is seeking an experienced Associate Director, Purification Process Development to join our team in South San Francisco. As a key member of our Purification Process Development team, you will be responsible for designing, executing, and reporting purification processes for the development and manufacture of Ad5 vectors used in oral vaccines.
Key Responsibilities- Manage lab-based purification development staff and contract service partners to provide data and informational support for development activities.
- Design and execute experimental protocols for purification development, and write/review protocols, purification development reports, batch records, standard operating procedures, and other technical reports in support of manufacturing and process tech transfer.
- Evaluate new technology and procedures, and apply data generated from experiments and literature to modify/optimize process parameters.
- Manage and train staff as appropriate in laboratory activities, and ensure that training and compliance records for themselves and staff are up to date and appropriate.
- Proactively communicate with internal and external stakeholders, and establish and foster relationships with contract manufacturing organizations.
- BS or MS in Bioengineering, Biochemistry, or other appropriate fields, or 8 years of relevant industry experience, and a Ph.D. in Bioengineering, Biochemistry, or closely related field with 5 years of relevant experience.
- A minimum of 2 years of prior management experience.
- 8 years of relevant industry experience.
- Strong experience with production and purification of viral products, and experience with viral product purification is a significant enhancement.
- Familiarity with mammalian cell culture in a GMP environment.
- Strong communication and teamwork skills, and ability to gain cooperation of others.
- Strong experience with general or direct supervision to exempt employees and/or skilled nonexempt employees.
- Strong knowledge of QC issues.
- Experience in relevant Regulatory filings for PD output and knowledge of Regulatory requirements and regulations.
- Expert in sterile techniques and hazardous/infectious material handling.
Vaxart Inc. is a clinical-stage biotechnology company developing a range of oral recombinant vaccines based on its proprietary delivery platform. Our mission is the promotion of global health through the development of effective vaccines that can be administered by tablet rather than by injection, providing for the simple and efficient distribution and administration of safe vaccines in any setting.
We are committed to the principles of equal employment opportunity and affirmative action for all applicants and employees. Equal opportunity and consideration are afforded to all qualified applicants and employees in personnel actions, which include recruiting and hiring, selection for training, promotion, rates of pay or other compensation, transfer, discipline, demotion, and layoff or termination.
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South San Francisco, California, United States Vaxart Inc. Full timeJob SummaryVaxart Inc. is seeking an experienced Associate Director, Purification Process Development to join our team in South San Francisco. The successful candidate will be responsible for designing, executing, and reporting purification processes for the development and manufacture of Ad5 vectors used in oral vaccines.This is a critical role that...
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