Engineer, Downstream Process Development & MSAT

United States·CambridgeFull-Timemid

OtherDevelopment

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Quick Summary

Overview

Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe,

Technical Tools

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Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.

Summary of Position:

The Technical Operations Department at Scholar Rock is seeking a scientifically curious and motivated engineer in the Downstream PD & MSAT group. The successful candidate is expected to be proficient in all aspects of the purification process and be comfortable working with a multifunctional team. Experience in late-stage process development and support of external manufacturing is preferred. The selected candidate will work alongside in-house scientists to advance existing projects through the development lifecycle and transfer to CMOs.

Proficiency in AKTA operation, TFF, VRF, JMP for data trending and presentation, and design of experiment skills are key traits that will ensure success in this role.

Support external manufacturing of clinical and commercial assets

Own and maintain process monitoring databases (CPV and lot history)

Support manufacturing campaign readiness review process

Drive batch production record review processes

Author and drive Downstream change control implementation

Work closely with CDMO to support tech transfer and manufacturing activities

Technical presentation to greater TechOps team

Support process development experiments to develop, optimize, and characterize purification processes for antibodies.

Detailed documentation of all experimental studies

Educational background in Chemical Engineering, Biochemistry, Biotechnology, or related biological Sciences.

Direct experience working with mAbs is preferred, and MSAT experience is highly desirable

BS with 6+ years of experience