The Associate Scientist II will design and execute assays, collaborate on method validation, prepare data for stakeholders, and develop analytical methods for gene therapy products.
Here at Kelonia Therapeutics, we aren’t just a clinical company; we’re trailblazers in viral engineering, pushing the boundaries of in vivo lentiviral gene and cell therapy. We're not just a team; we're dreamers on a mission to bring the promise of cell and gene therapy to every patient in need.
We've gathered a group of pioneers in cell and gene therapy to lead our journey, with extraordinary scientific founders at the helm, providing the cutting-edge technology that sets us apart. We're not just building a company; we're cultivating a culture that values both skill and care.
Are you ready to be a part of our remarkable journey? We're looking for someone exceptional to join our growing team as an Associate Scientist II in the Analytical Development group. This isn't just a job; it's an opportunity to contribute to groundbreaking therapies, to be part of a company's inception, and to make a transformative impact on patients' lives. If you're passionate about scaling a company from the ground up, making a real difference, and shaping the inclusive culture we're proud of, this opportunity is tailor-made for you. Join us and be a driving force in achieving excellence in viral engineering.
What You'll Do:
- Design and execute assays for characterization and in-process testing and collaborate with senior AD personnel to interpret results
- Review and execute qualification and validation protocols of analytical methods
- Prepare and present data and interpretations to cross-functional stakeholders
- Author and maintain analytical procedures and ensure cross-functional training and implementation
- Develop and qualify analytical methods to release and characterize Kelonia’s injectable gene therapy products
- Serve as subject matter expert in collaborative development and tech transfer of analytical methods between internal stakeholders and external AD and QC organizations
What You'll Bring:
- M.S. in biochemical engineering, biology, biochemistry, or related field with 0+ years of industry experience, or B.S. with 2+ years of experience
- Ability to communicate effectively with internal and external stakeholders
- Experience writing and revising SOPs and writing and executing protocols and reports for non-GMP activities in support of regulatory filings and/or process changes
- Experience with cellular assays (examples: MSD/Luminex/ELISA, multicolor flow cytometry) and/or molecular assays (examples: qPCR/PCR/ddPCR)
- Experience with assay qualification and validation is a plus
- Experience with viral vector titer methods is a plus
- Experience with liquid handlers and automation is preferred
- Excellent organizational and documentation skills
- Must work collaboratively, meet deadlines, and balance multiple workstreams according to group/company priorities
At Kelonia, we’re serious about balance and growth. You’ll get Flexible Time Off, flexible scheduling that aligns with your needs and our objectives, a competitive benefits package (health, commuter, and more), and great on-site perks that include free parking, a state-of-the-art gym, and a food hall – all within a collaborative, inclusive team that invests in your development and makes big things happen together.
Kelonia Therapeutics is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law. Kelonia does not accept unsolicited resumes from any source other than directly from candidates.
Job Type: Full-time
Work Type: On-Site M-F
Location: Boston, MA
Top Skills
Ddpcr
Elisa
Luminex
Msd
Multicolor Flow Cytometry
Pcr
Qpcr
Kelonia Therapeutics Boston, Massachusetts, USA Office
Boston, Massachusetts, United States
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