Analytical Development Principal Research Associate (Contract)

Vertex Pharmaceuticals • Boston, MA

1d • $43 - $48 • Onsite

About The Position

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.

Requirements

• Strong hands-on experience with cell culture and aseptic technique.
• 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.

Nice To Haves

• Experience with stem cell or immune cells is a plus.
• Knowledge of and hands-on experience with analytical method development, including characterization and release assays

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.

Benefits

• compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer.
• eligible for overtime pay, in accordance with federal and state requirements

What This Job Offers

• Job Type: Full-time
• Career Level: Senior