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Dyne Therapeutics

Waltham, Massachusetts, United States

Posted on: 14 March 2024

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Senior Scientist Bioanalysis

Role Summary:

This role plays a critical role in advancing our pipeline of novel treatments through the application of cutting-edge bioanalytical techniques. This includes designing, developing, optimizing, and validating bioanalytical in complex biological matrices with a focus on muscle tissue and fluids. The person in this role is expected to utilize state-of-the-art LC-MS/MS instrumentation for the quantitative analysis of biomarkers, metabolites, and therapeutic compounds in preclinical and clinical samples.

This role is based in Waltham, MA without the possibility of being a remote role. Candidates must be able to relocate.

Primary Responsibilities Include:

  • Provide bioanalytical support for portfolio, including complex method development and troubleshooting for PK and immunogenicity assays across several programs.
  • Collaborate cross-functionally with Platform, Research and Non-Clinical teams.
  • Design, develop and/or optimize sensitive quantitative assays to measure Dyne proprietary drugs in different matrices (plasma, urine, tissues) and from different species (rodents, non-human primates, human).
  • Setup and maintain lab instrumentation.
  • Evaluate assay performance, ability to troubleshoot issues.
  • Perform data analysis and interpretation.
  • Track progress against project timelines, generate regular status updates, and communicate progress and issues to management.
  • Maintain a well-documented laboratory notebook.
  • Effectively manage workload with minimal supervision.
  • Adhere to safe laboratory practices.
  • Multi-task across several projects and manage time effectively to achieve results.
  • Collaborate to identify external vendors (CRO) for new outsourced projects and request contracts.
  • Transfer bioanalytical assays to CROs, oversee assay validation and sample testing. 

Education and Skills Requirements:

  • BS or MS in Pharmaceutical sciences with at least 6-8 years of experience in the pharmaceutical industry or PhD degree with at least 4 years of industry experience
  • Broad, and in-depth knowledge of FDA bioanalytical guidance to industry
  • Hands-on assay development experience with different ligand binging assay formats and detection methods required
  • Strong assay troubleshooting, data analysis and interpretation skills
  • Excellent verbal and written communication skills
  • Ability to work collaboratively in a team-oriented environment
  • Strong attention to detail, organizational skills, and ability to multitask
  • Demonstrated ability to troubleshoot and solve problems

 

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