Senior Scientist, Analytical Development
About the role
Aurion Biotech is seeking a highly motivated Senior Scientist, Analytical Development in Cambridge, MA. This position will serve as an integral part of a multidisciplinary team to develop, qualify, and transfer in-process control, characterization, and release assays to support early and late-stage clinical manufacturing and testing of cell therapy products. The individual in this role will work collaboratively with the Research, Process Development, Quality and other groups to make sure assays meet the timeline of characterization and release of cell therapy products.
Key responsibilities
- Conduct various independent laboratory experiments including but not limited to Flow Cytometry, cell counting, dPCR, qPCR, ELISA, cell-based potency assays etc. to satisfy the overall AD objectives.
- Collaborate cross-functionally with other functions including Cell Production, Process Development, Manufacturing, and Quality.
- Author method qualification SOP, method qualification report and test method SOP and other technical documents to support regulatory submissions and other groups.
- Track progress toward project milestones and ensure that deliverables are met.
- Responsible for the development, optimization, qualification, and transfer of GMP-compliant analytical methods and materials that meet US FDA and/or EU regulatory requirements for clinical stage, cell therapy products.
- Train other groups to execute various in-house assays.
- Experience with Quality Control and regulatory requirements for late-stage method development and documentation are highly preferred.
- Other duties as assigned.
About Aurion Biotech
Aurion Biotech is a clinical-stage biotech company based in Seattle, Boston, and Tokyo. The Company's mission is to restore vision to millions of patients with life-changing regenerative therapies. The Company's first candidate is for the treatment of corneal edema secondary to endothelial dysfunction, and one of the first clinically validated cell therapies for corneal care; it was recently granted regulatory approval from Japan's PMDA. Aurion Biotech is the recipient of the prestigious Prix Galien award for best start-up in biotech. The Company is growing rapidly and seeks to hire highly motivated candidates from diverse backgrounds, cultures, and experiences, who share our values:
- Stewardship: We make the world a better place for our patients, our communities, our clinicians, and our colleagues. We act responsibly as individuals, as employees, and as a company.
- Transformation: We embrace our challenges, our successes, and our failures. We are curious, we take risks, and we collaborate.
- Grit: We break down walls and strive to achieve the impossible. We are persistent and resilient, and we deliver on our commitments.
Lifestyle at Aurion Biotech
We want our people to wake up every morning excited and energized for work. We value employees, which is why we invest in making life at Aurion Biotech healthy, fun, and rewarding:
- Robust Benefits: We offer full health insurance to employees and their families, and all the acronyms: 401(k) matching, EAP, FSA, and generous PTO.
- Total Rewards: We offer competitive compensation packages to ensure all Aurion employees are rewarded for their hard work.
- Perks and Fun: Paid parking, subsidized commuter passes, in-office catered lunches, team events, and community projects are just a few ways that we bond, celebrate each other, have fun, and live our values.
- A PhD and 3-5 years’ experience or an MS degree and 6-8 years of experience in a relevant discipline (immunology, biochemistry, cell biology, biotechnology, or related field) in the pharmaceutical industry and academia, and specifically in gene and cell therapy.
- Experience with biological therapeutic products is critical, experience specifically with cell therapy technologies is preferred.
- Demonstrated track record with analytical development supporting early and late-stage development of cell therapies.
- Deep technical understanding of analytical method development for key assays (Flow Cytometry, automated cell counting, dPCR, qPCR, ELISA, cell-based potency) and associated requirements (validation, stability programs, comparability assessments, etc.) across development is required.