Associate Scientist II, Analytical Development

Kelonia Therapeutics • Boston, MA

9h • Onsite

About The Position

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.

Requirements

• 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)
• Excellent organizational and documentation skills
• Must work collaboratively, meet deadlines, and balance multiple workstreams according to group/company priorities

Nice To Haves

• 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

Responsibilities

• 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

Benefits

• Flexible Time Off
• flexible scheduling that aligns with your needs and our objectives
• a competitive benefits package (health, commuter, and more)
• great on-site perks that include free parking, a state-of-the-art gym, and a food hall
• a collaborative, inclusive team that invests in your development and makes big things happen together

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level