Senior Research Associate, GMU CMC

Job description

Position Overview:

The Senior Research Associate (SRA) will be a part of the Global Biologics Drug Product Development & Manufacturing group. The candidate will primarily support Biopharmaceutical Drug Product development projects for Gene Therapy (in support of the Genomic Medicine Unit) and Protein therapeutic programs. The candidate will have the opportunity to work on different facets of Biologics drug product development for different modalities such as gene therapy capsids (recombinant AAV and Lentiviral vectors), Lipid Nanoparticles, Cell Therapy and Protein therapeutics

Key Responsibilities:

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Execution of formulation, process development and stability studies with both liquid and lyophilized formulations.

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Work with internal and external partners to efficiently and comprehensively address formulation, stability and compatibility aspects using established assays, across a variety of technological platforms and disciplines.

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Planning, prioritization and initiation of concurrent experimental procedures for multiple programs to ensure their timely completion is essential.

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Provide technical mentorship to other team members.

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Take ownership of assigned studies to ensure timely completion.

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Maintain a strong work ethic and good documentation practices including electronic laboratory notebook maintenance and writing of technical reports and SOPs.

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Analyze, compile and present results to internal and cross functional teams comprised of members from multiple groups and stakeholders.

Basic Qualifications:

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Master’s degree in biochemistry, pharmaceutical science, chemical engineering or a related discipline or a Bachelor’s degree with a minimum of 2 years of relevant industry experience.

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Knowledge of analytical and biophysical characterization techniques such as HPLC, SDS-PAGE, cIEF, DSC, DLS, CD, HIAC, MFI, KF, XRD and fluorescence spectroscopy. Previous experience a plus.

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Excellent communication skills.

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Ability to multi-task and learn new skills and possess flexibility and adaptability that is needed in a fast-paced team environment

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Excellent teamwork and collaboration skills.

Advanced/Preferred Qualifications:  

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Experience of handing and working with viral gene delivery vectors is a significant plus.

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Knowledge of lyophilization, DP process modeling, container closure integrity and scale-up to support technology transfer is an added benefit.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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