Scientist
Camris International

Bethesda, Maryland

This job has expired.


Overview

CAMRIS is a clinical and life sciences firm that realizes innovative solutions to challenges worldwide through high-quality, cost-effective program and research management services. We combine our proven systems with today's most effective, evidence-based best practices to improve the lives of people around the world. Our core practice areas include HIV/AIDS, microbiology and infectious disease research, vaccine research, development and production, global health security, biodefense, and clinical research.

CAMRIS attracts the next generation of scientists to work at premier government research and development institutions with state-of-the-art facilities and equipment, under world leaders in health research. Our exceptional benefits package that includes medical, dental and vision coverage, 401k plan with employer contribution, paid holidays, vacation, Medical and Flexible Spending Accounts, and life insurance. If you enjoy being a part of a high performing health and research organization dedicated to making the world a healthier place, please apply today!

We are seeking a Scientist to provide services in support of the overall functions of the Vaccine Production Program.

Responsibilities

  • Coordinate and execute formulation and stability studies within a development team, including internal and interdepartmental coordination of activities as well as collation and interpretation of study data, under direction of a Formulation Scientist/Senior Scientist.
  • Write and review formulation, stability, and method development study protocols under direction of a Formulation Scientist/Senior Scientist.
  • Independently generate and analyze samples using both standard and advanced study specific analytical methods.
  • Independently analyze and collate analytical data.
  • Interpret analytical data with an understanding of protein/vaccine structure and stability concepts, and elements of the effects of solution components on stability.
  • Develop assays for vaccine and biotherapeutic characterization, including providing input into study design, under direction of a Formulation Scientist/Senior Scientist.
  • Provide technical guidance and training to formulation team members.
  • Write and review technical reports and protocols documenting formulation, stability, and method development studies.
  • Present data in small group, department, and conference settings.
  • Obtain information on new scientific advances in the field and new technologies, as required to for VRC programs
  • Oversee external service and execute routine maintenance and troubleshooting for one or more pieces of laboratory instrumentation.
  • Serve as Subject Matter Expert for one or more analytical and/or theoretical areas relevant to the formulation development program.


Qualifications

  • B.S. in Chemistry, Biochemistry, Chemical Engineering, or a related discipline.
  • 4 years (minimum) industry, government or equivalent experience in protein formulation or a related field. OR
  • M.S. in Chemistry, Biochemistry, Chemical Engineering, or a related discipline.
  • 2 years (minimum) industry, government or equivalent experience in protein formulation or a related field.
  • Experience with study coordination and execution in one or more of the following areas: protein/vaccine formulation, protein/vaccine stability, protein/vaccine pre-formulation or related biophysical characterization/development.
  • Hands-on experience, including data analysis and basic theoretical knowledge, with three or more of the following techniques: UV-visible, fluorescence, Circular Dichroism and/or IR spectroscopy; Differential Scanning Calorimetry; Particle characterization (light scattering, subvisible particle analysis, HIAC, and/or MFI).
  • Strong knowledge of protein chemistry and biophysical properties of proteins.
  • Knowledge of standard biophysical and bioanalytical methods and underlying theory.
  • Experience with data analysis using standard and specialized software platforms (JMP, Origin, GRAMS, Prism, SigmaPlot, etc.).
  • Strong time management skills and experience balancing multiple projects.
  • Strong written, oral, and visual communication skills.
  • Ability to work independently.
  • Proficiency with Microsoft Word, PowerPoint, or other equivalent software suites.


CAMRIS International LLC offers competitive salaries and comprehensive benefits. Please submit your resume online at www.CAMRIS.com . CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, or any other characteristic protected by any applicable federal, state, or local law.

Full vaccination against COVID-19, defined as two doses of Moderna, two doses of Pfizer, or one dose of Johnson & Johnson's Janssen, is required for this position.

Employment is contingent upon successful completion of a Public Trust-level background check, a requirement for this position under an active federal contract. The background check process may include, but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment, education and credentials; (3) a criminal background check; (4) use/abuse of federally-controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully-complete any required background check questionnaire during initial onboarding.


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