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What are the key skills and qualifications needed to thrive as a biotechnology professional at Solid Biosciences Inc, and why are they important?

To thrive as a biotechnology professional at Solid Biosciences Inc., you need a strong background in molecular biology, genetics, and biochemistry, typically supported by a relevant degree in life sciences. Experience with laboratory techniques (such as PCR, Western blotting, and cell culture), as well as familiarity with data analysis software and regulatory compliance, is highly valued. Attention to detail, problem-solving skills, and the ability to work collaboratively are essential soft skills in this field. These capabilities ensure accurate research outcomes, efficient teamwork, and compliance with industry regulations, which are critical for advancing innovative therapies.

What is the difference between Solid Biosciences Inc vs Solid Biosciences Inc Research Associate?

AspectSolid Biosciences IncSolid Biosciences Inc Research Associate
CredentialsBachelor's or Master's in Life SciencesBachelor's or Master's in related field, some roles prefer lab experience
Work EnvironmentResearch labs, corporate officesLaboratory settings, experimental work
Industry UsageBiotech research and developmentSupporting research projects, data collection, lab experiments

Solid Biosciences Inc is a biotech company focused on gene therapy research, while a Research Associate at Solid Biosciences Inc typically supports research activities within the company. The main difference lies in roles: Solid Biosciences Inc refers to the organization, whereas the Research Associate is a specific position involved in hands-on research tasks.

What are some common challenges faced by employees working at Solid Biosciences Inc, and how does the company support its teams?

Working at Solid Biosciences Inc., professionals often encounter the challenge of navigating the complexities of drug development in the rare disease space, where timelines can be uncertain and scientific hurdles are significant. The company fosters a collaborative environment, encouraging cross-functional teamwork among research, clinical, and regulatory teams to overcome obstacles. Solid Biosciences Inc. also invests in professional development and open communication, supporting employees through mentorship and regular feedback to help them grow and adapt to evolving project needs.

What does Solid Biosciences Inc do?

Solid Biosciences Inc is a biotechnology company focused on developing therapies for rare neuromuscular and cardiac diseases, with a primary emphasis on Duchenne muscular dystrophy (DMD). The company utilizes innovative gene therapy and precision medicine approaches to address unmet medical needs in these patient populations. Solid Biosciences conducts research, clinical development, and collaborates with partners to advance potential treatments from the laboratory to patients.
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Solid Biosciences Inc jobs near you
Infographic showing various Solid Biosciences Inc job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 1% Temporary, and 6% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Principal Associate Scientist

Solid Biosciences

Charlestown, MA • On-site

$110K/yr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Solid Biosciences, Inc. (Charlestown, MA) seeks Principal Associate Scientist, Analytical Development as follows:

Job Description:

  • Summary: Responsible for analytical development, qualification and operational support for Preclinical, Phase 1 and Phase 3 of clinical products.
  • Support the development and execution of analytical methods directly related to process development cGMP manufacturing of Solid Biosciences leading candidate.
  • Lab operation: routine and non-routine analytical testing, coordination with internal/external PD or cGMP Manufacturing, critical reagent qualification, maintain laboratory equipment, maintain laboratory inventory, compile and present data to support process development and stability.
  • Analytical Development: support the development of new methods by identifying, evaluating and executing analytical methods to support ongoing analytical needs.
  • GMP manufacturing: participate in the support of manufacturing activities at CMOs and CTOs related to analytics including coordinating testing, shipments, inventory, data review and reporting.
  • Maintain well documented records of analytical data, laboratory notebooks, execution of assays and stability data.
  • Act as subject matter expert and involved in updates to Operational and Senior Management teams.
  • May have responsibility for management and mentorship of junior scientists.
  • Technology Transfer: Participate in tech transfer of analytical methods, protocols/procedures and know-how from internal labs to CMOs/CTOs, or between CMOs/CTOs.
  • Contribute towards assay qualification at CMOs/CROs.
  • Travel required 10% of the time, domestic only.

Job Requirements:

  • Master’s of Science in Biotechnology, Microbiology, Biology, Genetics or related field (or foreign equivalent).
  • Two (2) years of experience in analytical development or quality control within a biotech/pharmaceutical process development or manufacturing environment.
  • One (1) year of experience with molecular and cell based analytical methods including cell culture, In vitro cell based assays, ddPCR, qPCR, ELISA.
  • One (1) year of experience working in cGMP supporting analytical development/Quality control environment with an understanding of regulatory requirements and trends related to product quality.
  • One (1) year of experience with Electronic Lab Notebook (ELN).
  • One (1) year of experience with compliance and cGMP considerations.

Salary: $110,000.00