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Analytical Development Principal Research Associate

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: Vertex Pharmaceuticals
Contract position
Listed on 2026-09-16
Job specializations:
  • Research/Development
    Biotech Research, Regulatory Compliance Specialist, Research Scientist
Salary/Wage Range or Industry Benchmark: 43 - 48 USD Hourly USD 43.00 48.00 HOUR
Job Description & How to Apply Below

Job Description

The Analytical Development Principal Research Associate performs and supports analytical method development activities for cell therapy products and other biologics. In this on-site role, you will perform laboratory-based experiments, execute sample testing and data analysis, maintain high-quality documentation, and support assay troubleshooting and optimization. This position is ideal for a collaborative, detail-oriented scientist who thrives in a fast-paced environment and is excited to contribute to advancing innovative therapies.

Key

Duties and Responsibilities
  • Lead and execute laboratory experiments to support analytical method development, optimization, qualification, and lifecycle management for cell therapy and biologics programs.
  • Independently design, plan, and conduct sample testing and data analysis, exercising strong scientific judgment to ensure high-quality and timely results.
  • Maintain clear, accurate, and compliant documentation of experiments, studies, and results in accordance with GMP-like practices and departmental standards.
  • Author, review, and revise SOPs, protocols, technical reports, study plans, and other controlled documents.
  • Present data, project updates, and technical recommendations to internal teams and cross-functional stakeholders.
  • Work safely and effectively in a GMP-like laboratory environment while promoting compliance, quality, and operational discipline.
  • Manage multiple priorities independently, balancing day-to-day execution with longer‑term project goals and team objectives.
  • Perform other duties as assigned.
Required Knowledge and Skills
  • Strong hands‑on experience with cell culture and aseptic technique. Experience with stem cell or immune cells is a plus.
  • Demonstrated experience with analytical methods relevant to cell therapy and/or biologics, including one or more of the following:
    flow cytometry and immunostaining‑based imaging
    .
  • Working knowledge of GMP‑like laboratory practices, documentation requirements, and quality/compliance expectations.
  • Excellent problem‑solving and troubleshooting skills, with the ability to evaluate complex issues and implement effective solutions.
  • Strong verbal and written communication skills, with the ability to clearly present technical information to multidisciplinary and matrixed teams.
  • Proven ability to build collaborative relationships and influence across functions, contributing effectively in a fast‑paced, team‑oriented environment.
  • Strong organizational and prioritization skills, with the ability to manage multiple tasks and deliver high‑quality results in a dynamic environment.
Required Educational Level
  • Bachelor’s degree (or equivalent degree) in Biology, Chemistry, or equivalent and at least 5 years of experience
  • Master’s degree (or equivalent degree) in Biology, Chemistry, or equivalent and at least 2 years of experience
  • In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related academic/vocational experience, will be considered sufficient for an individual to meet the requirements of the role
Preferred Experience
  • Knowledge of and hands‑on experience with analytical method development, including characterization and release assays
Working Environment
  • This is an onsite position at our Boston LC1 site.
  • Ableto work upright and stationary and/or standingfor typical working hours.
  • Able to use and learn standard office equipment and technology with proficiency.
  • Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
Pay Range

$43-$48/HR

No C2C or Third-Party Vendors
Position Requirements
10+ Years work experience
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