On-Site
Full Time
Intermediate or Experienced
$94,000 to $181,000 a year
Waltham, Massachusetts, United States
About Dash Bio
Our Mission:
Dash accelerates drug development. By fusing advanced automation-native lab workflows and integrated software into a unified platform, we provide the biopharma industry with the high-velocity, high-quality, data-driven development solutions required to get life-saving therapies to patients faster. Dash seeks to continuously improve industry KPIs and materially reduce the time and cost to bring a drug to market.
Company Summary:
We are building the infrastructure for modern drug development. We are moving beyond the manual, fragmented processes of traditional service providers by taking a technology-first approach to bioanalysis. Our platform is tech-enabled, automated, and GLP-compliant with the goal to industrialize the scientific workflows that act as bottlenecks in the industry. We deliver next-generation preclinical and clinical bioanalysis results with unprecedented speed and precision.
We are a team of builders operating at the intersection of biology, hardware, and code. This is an environment for scientists and engineers who are tired of the status quo and are ready to apply their skills to solve hard problems at scale. We don't just run assays, we architect the systems that will define the future of drug development.
We are a place where employees are stretched to do the best work of their career. We are looking for engineers, scientists, and biotechnicians who want to make an impact on the world and leverage their skills in an innovative way.
About the job
Job Description:
Dash Bio is seeking a scientifically curious, adaptable, and intellectually driven individual to develop and implement bioanalytical methods that power our highly automated clinical bioanalysis lab. You'll work at the intersection of biology, automation, and software, translating fundamental scientific principles into scalable, robust assays that run reliably on our tech-first platform.
We value scientific versatility over narrow specialization. The ideal candidate is someone who thrives on learning new techniques, approaches problems systematically, and can rapidly adapt their expertise across different analytical platforms. This is an on-site role partnering closely with Automation, Quality, and Software teams to bring methods from concept through validation. Level will be matched to experience (Associate Scientist through Senior Scientist).
Key Responsibilities:
Method Development and Innovation:
- Design, optimize, and troubleshoot analytical assays across multiple platforms including immunoassays (ELISA, MSD/ECL, Luminex), and cell-based/ligand-binding assays for PK, immunogenicity (ADA/NAb), and biomarker applications.
- Rapidly acquire proficiency in new analytical techniques and platforms as business needs evolve, demonstrating intellectual agility and systematic approach to method learning.
- Apply fundamental scientific principles to solve complex technical challenges, often bridging concepts from molecular biology, biochemistry, and analytical chemistry.
- Collaborate with automation engineers to translate manual protocols into robust automated workflows on liquid handlers and integrated robotics (e.g., Hamilton, KingFisher, Omni); contribute to script design, QC checkpoints, and error-handling strategies.
- Partner with software and data science teams to optimize data capture, LIMS integration, and analytics pipelines, ensuring seamless information flow and rapid turnaround.
Technical Excellence and Problem-Solving:
- Systematically troubleshoot assay performance issues using data-driven approaches and scientific reasoning rather than cookbook methodologies.
- Establish and manage critical reagent qualification programs, reference standards, calibrators, and controls; design and execute bridging studies and lot-to-lot comparability assessments.
- Define comprehensive sample handling workflows including matrix selection, stability protocols, freeze-thaw studies, parallelism, and selectivity assessments for challenging clinical specimens.
- Use design of experiments (DOE) and statistical methods to establish assay performance characteristics including sensitivity/LOD/LOQ, precision, accuracy, specificity, linearity/range, robustness, and stability.
Documentation and Regulatory Alignment:
- Author clear, scientifically rigorous method development reports, validation plans/protocols, and validation reports aligned with ICH M10 and FDA bioanalytical guidance.
- Define control strategies, acceptance criteria, and system suitability parameters; implement qualified/validated methods for GLP operations in collaboration with automation teams.
- Communicate complex technical findings to diverse audiences including internal teams and external clients, translating data into actionable insights that drive project strategies and regulatory submissions.
Leadership and Collaboration:
- Manage multiple concurrent projects while maintaining quality standards, timelines, and regulatory compliance requirements.
- Mentor junior scientists and technicians, providing hands-on guidance in experimental design, data interpretation, and adherence to scientific best practices.
- Serve as technical subject matter expert during client interactions and regulatory discussions, representing assay development capabilities and limitations accurately.
- Foster a culture of scientific curiosity, continuous learning, and cross-functional collaboration across all departments.
- Contribute to strategic planning and innovation initiatives, bringing fresh perspectives from diverse scientific backgrounds.
Qualifications:
Required:
- BS/MS/PhD in Life Sciences (Biochemistry, Molecular Biology, Bioengineering, or related field) with 3+ years of hands-on research experience
- Demonstrated track record of mastering new laboratory techniques and analytical methods across different research environments
- Strong foundation in analytical method development principles including optimization, troubleshooting, and performance characterization
- Experience with quantitative data analysis, statistical methods, and experimental design
- Proven ability to work independently while collaborating effectively in multidisciplinary teams
- Excellent scientific communication skills with attention to detail and systematic approach to problem-solving
- Intellectual curiosity and adaptability to rapidly evolving technical requirements
Preferred:
- Experience with automated liquid handling systems and laboratory robotics platforms
- Background in immunoassays (ELISA, MSD) or cell-based assays
- Experience in Flow cytometry and/or FACS
- Familiarity with GxP environments, method validation, and regulatory guidelines
- Track record of translating methods across different analytical platforms or research contexts
- Experience bridging wet lab techniques with data analysis and computational approaches
- Exposure to Cell cultures
In accordance with Massachusetts pay transparency requirements, the base salary range for this role is $94,000-$181,000. Actual compensation will vary based on experience, skills, scope, responsibilities, and internal equity. |
Benefits
Health Insurance
Dental Insurance
Vision Insurance
401(k) Matching
Paid Time Off (PTO)
Paid Holidays
Sick Leave
Bonus
Preferred Skills
glp
elisa
msd
cell based assays
gxp
What We Offer:
- Opportunity to work at the forefront of bioanalytical innovation.
- Collaborative and inclusive company culture.
- Competitive salary and comprehensive benefits package.
- Direct access to industry veterans and a supportive environment for professional growth.