Co-op, Parenteral Drug Product Development

Biogen•Cambridge, MA

About The Position

About the Role: This application is for a 6-month student role from July - December 2026. Resume review begins in January 2026. As a Co-op in Parenteral Drug Product Development, you will be an integral part of the team focused on the study and testing of various oligonucleotides across diverse formulations and steam sterilization conditions. This role offers hands-on experience in formulation science and sterilization techniques, providing an invaluable learning opportunity that enriches your resume. You will contribute to internal reports as a co-author, enhancing your research and writing skills. This position allows you to immerse yourself in departmental meetings, gaining a comprehensive understanding of oligonucleotide drug product development within the pharmaceutical industry. Additionally, you will present your research findings in both oral and written formats, further developing your communication skills. Collaborating closely with a pharmaceutical scientist, you will engage in a research project that plays a crucial role in advancing our development efforts. What You’ll Do: During the co-op appointment, they will work closely with a pharmaceutical scientist on a research project with key tasks that include, but not limited to, the following:

Requirements

Should have basic laboratory skills and research experience, such as recording in lab notebook, aseptic manufacturing techniques (buffer exchange, filtration, sterilization), analytical techniques (ultra high-pressure liquid chromatography, spectroscopy), and safe lab practices.
To participate in the Biogen Internship or Co-op Program, students must meet the following eligibility criteria: Legal authorization to work in the U.S. At least 18 years of age prior to the scheduled start date. Currently enrolled in an accredited community college, college, university or skills program/apprenticeship.
Must have completed a minimum of two years of study toward a bachelor’s degree by May 2026.

Nice To Haves

Knowledge of synthetic oligonucleotides development (chemistry, manufacturing, and controls) and statistical analysis by JMP® is a plus

Responsibilities

Planning and executing research related to the development of steam-sterilization process
Utilization of a variety of physical and chemical characterization techniques to develop an understanding of the physicochemical characteristics of oligonucleotides and associated formulations.
Utilization of modeling tools to assess formulation stability and performance
Development of small-scale pre-formulation screening workflow to predict formulation performance