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Guidehouse

Advises agencies and runs regulated operations

Bioassay Researcher

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeSilver Spring, MD, USA

About the Job

Requirements

  • A master's degree in Chemistry, Biology, Biochemistry, Cell Biology, Bioengineering, Pharmaceutical Sciences, or a related scientific discipline is required.
  • Three to six years of experience developing, optimizing, validating, or implementing bioassays for therapeutic proteins, peptides, biotechnology products, biosimilars, or complex generics are required.
  • Experience with laboratory techniques such as quantitative reverse transcription polymerase chain reaction, enzyme-linked immunosorbent assay, western blotting, immunohistochemistry, or related analytical methods is required.
  • Experience collecting, processing, analyzing, and documenting laboratory data in accordance with project plans and quality standards is required.
  • Experience preparing scientific manuscripts, technical reports, presentations, and research summaries is required.
  • Knowledge of Good Laboratory Practices, International Organization for Standardization laboratory standards, or equivalent laboratory quality systems is required.
  • Understanding of regulatory interpretations, product efficacy and safety considerations, project plans, and timelines is required.
  • The ability to work effectively within interdisciplinary scientific teams in a laboratory research environment is required.
  • The ability to complete required corporate and client training and maintain necessary credentials is required.

Responsibilities

  • Provide scientific and laboratory research support to establish, characterize, optimize, and validate bioassays for biological therapeutics.
  • Culture and maintain mammalian and immortalized cell lines using aseptic laboratory techniques.
  • Develop and optimize cell-based transcytosis and permeation bioassays to evaluate transport of biological therapeutics across epithelial cell layers.
  • Validate established bioassays against defined performance criteria, including reproducibility, sensitivity, and specificity.
  • Perform laboratory techniques including cell culture, quantitative reverse transcription polymerase chain reaction, enzyme-linked immunosorbent assay, western blotting, immunohistochemistry, and other biochemical or molecular assays.
  • Conduct surveillance testing and investigate mechanisms of action of therapeutic proteins and peptides to identify relevant assay readouts.
  • Establish new analytical methods to evaluate the biological activity of biotechnology products, biosimilars, and complex generics.
  • Collect, process, analyze, and document laboratory data from multiple sources and databases in accordance with project plans.
  • Maintain complete and accurate laboratory notebooks, experimental records, methods, and analyses in accordance with Food and Drug Administration laboratory standards.
  • Assist with laboratory inventory management, procurement, equipment maintenance, and instrument upkeep.
  • Prepare technical reports, scientific manuscripts, status reports, presentations, and final project summaries supporting regulatory decision-making.
  • Participate in interdisciplinary scientific collaborations and support approved research projects.
  • Provide weekly program updates and monthly project status reports detailing research findings, milestone progress, risks, and issues.
  • Attend relevant scientific, laboratory, programmatic, and organizational meetings in support of project execution.
  • Communicate complex scientific findings and project updates to technical and non-technical stakeholders.

Desired Qualifications

  • A Ph.D. in Chemistry, Biotechnology, Biology, Biochemistry, Cell Biology, Bioengineering, Pharmaceutical Sciences, or a related scientific discipline is preferred.
  • Experience developing potency, functional, or mechanism-of-action bioassays for biologics, biosimilars, biotechnology products, or complex generics is desirable.
  • Experience with air-liquid interface cultures, epithelial cell models, transcytosis assays, permeability assays, or related in vitro transport models is desirable.
  • Understanding of biopharmaceutical manufacturing, process development, biotechnology research, and regulatory operations is desirable.
  • Knowledge of insulin and GLP-1 receptor signaling pathways or related biological systems is desirable.
  • Experience preparing peer-reviewed publications, scientific posters, regulatory science reports, or white papers is desirable.

About the Company

Guidehouse

Advises agencies and runs regulated operations

Guidehouse advises government agencies and companies in regulated industries on strategy, technology and day-to-day operations. Its work combines business advice with software implementation and ongoing management, so a client uses the same firm to plan a change, build the systems and run the resulting processes. Teams modernize cloud platforms, apply data analysis and artificial intelligence, and redesign organizations to meet operating and regulatory requirements. Clients pay for consulting projects and technology work or outsource continuing business functions to its managed services teams. Guidehouse was founded in 2018 and is headquartered in McLean, Virginia.

Company size
10,001+
Company stage
Acquired
Total funding
$750K
Headquarters
McLean, VA
Founded
2018

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