Analytical Development Principal Research Associate (Contract)

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

• Bachelors degree (or equivalent degree) in Biology Chemistry or equivalent and at least 5 years of experience
• Masters 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 technologywith proficiency.
• Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

$43-$48/HR

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (Vertex). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation medical benefits fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors including skills competencies experience location and/or being pursued and other job-related factors permitted by addition this role will be eligible for overtime pay in accordance with federal and state requirements

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