Scholar Rock

Biopharmaceutical firm targeting protein growth factors

Senior Engineer - Downstream Manufacturing Science & Technology, Manufacturing Science & Technology

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours

Full-timeCambridge, MA, USA$120k - $175k /yr

About the Job

Requirements

A bachelor's, master's, or PhD in Chemical Engineering, Biochemical Engineering, Biotechnology, Biochemistry, or a related discipline, with relevant MSAT, process engineering, GMP manufacturing, technology transfer, or biologics manufacturing experience.
Relevant experience of 10+ years with a bachelor's degree, 8+ years with a master's degree, or 2–5 years with a PhD.
Experience supporting monoclonal antibody downstream manufacturing processes in a GMP environment.
Strong knowledge of chromatography, viral filtration, tangential flow filtration, and ultrafiltration/diafiltration operations.
Experience reviewing batch records, GMP manufacturing documentation, and technical reports.
Strong communication, organization, collaboration, and technical writing skills.

Responsibilities

Provide downstream process oversight for late-stage clinical and commercial manufacturing at contract development and manufacturing organizations, including campaign readiness, technical risk assessment, manufacturing planning, and execution support.
Serve as Person-in-Plant, as needed, for technology transfer, process performance qualification/process validation, and clinical or commercial manufacturing activities.
Provide timely technical support during critical manufacturing operations, including off-hours support when required.
Own and maintain process monitoring systems, manufacturing databases, lot histories, and continued process verification programs.
Analyze manufacturing performance through statistical trending and process monitoring tools to ensure processes remain in a state of control.
Support Annual Product Reviews, Product Quality Reviews, and ongoing commercial lifecycle management activities, including post-approval changes and continuous improvement initiatives.
Collaborate with Process Development teams to ensure effective transfer of process knowledge into GMP manufacturing operations.
Support or lead process characterization, process performance qualification, and process validation activities.
Contribute to the generation and execution of validation protocols, validation reports, and associated technical documentation.
Lead or support deviations, atypical results, process excursions, change controls, technical and risk assessments, corrective and preventive actions, and issue resolution for downstream manufacturing processes.
Present technical analyses, manufacturing trends, and process performance updates to cross-functional teams and leadership.
Review and author GMP manufacturing documentation, batch records, technical reports, and regulatory submission content.
Support health authority responses, post-approval changes, inspections, and regulatory interactions as the downstream process subject matter expert.
Author technical assessments, risk assessments, manufacturing support documents, and process monitoring reports.

Desired Qualifications

Experience with commercial biologics manufacturing, continued process verification, Annual Product Reviews, Product Quality Reviews, technology transfer, process performance qualification/process validation, deviation investigations, corrective and preventive actions, change control, regulatory support, contract development and manufacturing organization oversight, JMP/statistical trending, design of experiments, or process characterization.
Experience with AKTA systems or lab-scale downstream development.

Salary Range: 120000 to 175000 (Currency: USD) (Pay period: per-year-salary)

Scholar Rock is delivering muscle-targeted breakthroughs to transform the treatment of spinal muscular atrophy (SMA) and other rare neuromuscular diseases where muscle atrophy remains a critical unmet need.

As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the biopharmaceutical 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 about our neuromuscular franchise at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.

Summary of Position:

Scholar Rock is seeking a Senior Engineer, Downstream Manufacturing Science & Technology (MSAT), to provide technical leadership for monoclonal antibody downstream manufacturing across a global external manufacturing network. This role serves as the downstream process SME supporting commercial manufacturing, technology transfer, PPQ/process validation, CPV, investigations, change control, regulatory support, and lifecycle management.

The ideal candidate brings strong downstream biologics process expertise, significant GMP manufacturing experience, sound technical judgment, and the ability to partner effectively with CDMOs and internal Process Development, External Manufacturing, Quality, Regulatory, and Supply Chain teams. This role is expected to influence cross-functional decision-making and serve as a trusted technical partner across downstream manufacturing activities.

Position Responsibilities

External Manufacturing Support:

Provide downstream process oversight for late-stage clinical and commercial manufacturing at CDMOs, including campaign readiness, technical risk assessment, manufacturing planning, and execution support.

Serve as Person-in-Plant, as needed, for technology transfer, PPQ/process validation, and clinical/commercial manufacturing activities.

Provide timely technical support during critical manufacturing operations, including off-hours support when required.

Process Monitoring & Lifecycle Management:

Own and maintain process monitoring systems, manufacturing databases, lot histories, and CPV programs.

Analyze manufacturing performance through statistical trending and process monitoring tools to ensure processes remain in a state of control.

Support Annual Product Reviews (APRs), Product Quality Reviews (PQRs), and ongoing commercial lifecycle management activities including post-approval changes and continuous improvement initiatives.

Technology Transfer & Validation:

Collaborate with Process Development teams to ensure effective transfer of process knowledge into GMP manufacturing operations.

Support or lead process characterization, process performance qualification (PPQ), and process validation activities.

Contribute to generation and execution of validation protocols, validation reports, and associated technical documentation.

Investigations, Change Control & Technical Leadership:

Lead or support deviations, atypical results, process excursions, change controls, technical/risk assessments, CAPAs, and issue resolution for downstream manufacturing processes.

Present technical analyses, manufacturing trends, and process performance updates to cross-functional teams and leadership.

Documentation & Regulatory Support:

Review and author GMP manufacturing documentation, batch records, technical reports, , and regulatory submission content.

Support health authority responses, post-approval changes, inspections, and regulatory interactions as the downstream process SME.

Author technical assessments, risk assessments, manufacturing support documents, and process monitoring reports.

Candidate Requirements

Bachelor’s, Master’s, or PhD in Chemical Engineering, Biochemical Engineering, Biotechnology, Biochemistry, or a related discipline, with relevant MSAT, process engineering, GMP manufacturing, technology transfer, or biologics manufacturing experience.

BS with 10+ years, MS with 8+ years, or PhD with 2 - 5 years of relevant experience.

Experience supporting mAb downstream manufacturing processes in a GMP environment.

Strong knowledge of chromatography, viral filtration, TFF, and UF/DF operations.

Experience reviewing batch records, GMP manufacturing documentation, and technical reports.

Strong communication, organization, collaboration, and technical writing skills.

Preferred Qualifications

Experience with commercial biologics manufacturing, CPV/APR/PQR, technology transfer, PPQ/process validation, deviation investigations, CAPA, change control, regulatory support, CDMO oversight, JMP/statistical trending, DoE, or process characterization.

Experience with AKTA systems or lab-scale downstream development is desirable but not required.

Travel: Approximately 25% travel to support technology transfer, process validation, commercial manufacturing, and external manufacturing partners.

Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

About the Company

Scholar Rock

Biopharmaceutical firm targeting protein growth factors

Scholar Rock develops biopharmaceutical therapies by targeting protein growth factors to treat diverse diseases. Its work hinges on a proprietary drug discovery platform that identifies ways to modulate these growth factors, enabling creation of novel therapeutic solutions. The company advances its programs through research and development, and collaborates with other biopharmaceutical companies and research institutions, earning revenue via licensing agreements, milestone payments, and eventual product sales. Scholar Rock differentiates itself by focusing on protein growth factors and pursuing targets and indications that have been historically overlooked, with a strong emphasis on partnerships and patient-centric approaches. The overall goal is to deliver safe and effective therapies that improve patient outcomes by precisely modulating growth factor pathways through collaborative science.

Company size: 201-500
Company stage: IPO
Headquarters: Cambridge, MA
Founded: 2012

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