Senior Scientist

Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH).

Axle is seeking a Senior Scientist to join our vibrant team at the National Institutes of Health (NIH) supporting the National Institute of Allergy and Infectious Diseases (NIAID) located in Gaithersburg, MD.

• Paid Time Off and Paid Holidays
• 401K match up to 5%
• Educational Benefits for Career Growth
• Employee Referral Bonus
• Flexible Spending Accounts
  • Healthcare (FSA)
  • Parking Reimbursement Account (PRK)
  • Dependent Care Assistant Program (DCAP)
  • Transportation Reimbursement Account (TRN)

The Senior Scientist will lead vaccine and biologic formulation development and clinical stability projects for investigational drug products. The position combines scientific leadership, experimental planning, data interpretation, formulation characterization, regulatory document support, and mentoring.

• Lead multiple formulation development and clinical stability projects, including experimental design, timelines, data interpretation, and coordination with internal and external collaborators.
• Protect data integrity and provide technical, theoretical, and strategic guidance to project team members.
• Serve as a subject matter expert on pharmaceutical compounding and administration of investigational drug products.
• Evaluate stability and compatibility data to ensure pharmaceutical compounding and clinical administration methods meet target product profiles.
• Coordinate formulation analytical testing support, balance resource allocation, and monitor completion of deliverables.
• Prepare, review, edit, and verify technical reports and protocols for formulation, stability, and method development studies.
• Coordinate equipment maintenance and servicing and draft, review, and update relevant standard operating procedures.
• Maintain the clinical excursion reporting system, evaluate affected product quality, coordinate with stakeholders, and manage supporting documentation.
• Address product quality inquiries and author and review regulatory filings in collaboration with regulatory affairs staff.
• Develop assays and technologies for vaccine and biotherapeutic characterization, evaluate new instruments and methods, and confirm assay results.
• Coordinate scientific literature discussions and present research at national conferences and scientific meetings.
• Provide scientific interpretation and guidance to management, mentor junior scientists, and train users in data and analysis methods.

• Ph.D. in chemistry, biochemistry, chemical engineering, or a related discipline.
• Expert knowledge of protein chemistry, protein and vaccine formulation, and the bioanalytical and biophysical properties of proteins and vaccines.
• Extensive knowledge of pharmaceutical compounding requirements and clinical-use stability, with hands‑on experience in clinical stability evaluation studies.
• Extensive experience designing, executing, and interpreting protein or vaccine formulation and stability studies, with practical knowledge of development practices for clinical trials.
• Proven technical and theoretical expertise in one or more formulation science areas, such as biophysical characterization, particle analysis,…