Sr Associate Scientist in Cambridge, MA

Open to candidates willing to relocate at own expense Paid Parking required at this site Possibility of an extension

Must Have:

• Nanoparticle-based formulation development & analytical characterization.
• Open to new grad PHD level, in lab/ academic experience
• Research projects and peer-reviewed publications.
• Manager is open to Biotech, Pharma, and Academic experience (Must display 3 years of applicable experience)

Summary

• We are seeking a motivated Scientist to be part of a team focused on non-viral gene therapy formulation in the Genomic Medicine Unit.
• The successful candidate will play a key role in targeted non-viral formulation development and optimization for several different projects.

Specifically, the remit of the candidate will be to:

• Support the development of customized non-viral formulations.
• Apply scientific expertise and judgement to initiate, design and execute experiments in a time-sensitive manner.
• Maintain accurate experiment records and material inventory.
• Analyze and present experiment data clearly and effectively.
• Acts as an impactful contributor of project teams and transverse initiatives.
• Foster creativity, productivity, execution with a sense of urgency, scientific integrity and accountability. Maintains a collaborative culture.

Qualifications:

• PhD or Master’s plus minimum 3 years of experience in Pharmaceutics, Chemistry, Biomedical Engineering, Chemical Engineering, or related field with a strong background in nanoparticle-based formulation development & analytical characterization.
• Hands-on experience in nucleic acid drug formulation and development (especially nanoparticle delivery technologies) is required.
• Results-oriented, with a track record of significant contribution to research projects and peer-reviewed publications.
• Demonstrated ability to independently design, execute, interpret, and present experimental results.
• Flexibility to adapt to rapidly changing priorities and deadlines in a dynamic, fast paced industry and work environment.
• Experience in preparing high quality documents including technical reports, presentations, SOPs, experimental protocols, and regulatory filings.
• Excellent written and oral communication skills.

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