Purification Scientist

Joulé

Boston, MA

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JOB DETAILS
SALARY
$39.60–$45.40 Per Hour
SKILLS
Affinity Chromatography, Analysis Skills, Analytical Development, Biochemistry, Biology, Biotech and Pharmaceutical, Chemical Engineering, Chromatography, Column Chromatography, Cross-Functional, Data Quality, Detail Oriented, Documentation, Documentation Standards, Droplet Digital PCR (ddPCR), Equipment Maintenance/Repair, Experiment Design, GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), High Performance Liquid Chromatography (HPLC), Identify Issues, Ion Exchange Chromatography, Laboratory Equipment, Maintain Compliance, Manufacturing, Polishing, Process Development, Process Improvement, Safety Compliance, System Operations, UV Spectroscopy, Unicorn Library Management System
LOCATION
Boston, MA
POSTED
3 days ago

Job Title: Purification Scientist – Downstream Process Development
Location: Boston, MA
Hours/Schedule: Monday–Friday, 8 am to 5 pm
Compensation: $40.00 - $45.40/hr
Type: 12 month contract, Potential for extension or conversion to permanent

Overview

The Purification Scientist supports downstream process development for viral vectors, biologics, and recombinant proteins. This role focuses on executing and optimizing purification workflows, generating high-quality data, and supporting manufacturing readiness under GMP/GLP-aligned practices. The ideal candidate brings strong hands-on chromatography and ultracentrifugation experience, with the ability to troubleshoot processes and collaborate across technical teams.

Responsibilities

  • Execute purification workflows including CsCl density gradient ultracentrifugation, affinity chromatography (e.g., AVB, CaptureSelect), ion-exchange chromatography (AEX, CEX), and polishing steps

  • Operate AKTA systems (Avant, Pure, or Pilot) to perform small- to large-scale purification runs

  • Perform tangential flow filtration (TFF) for concentration and buffer exchange of intermediates and final products

  • Design and execute experiments to support process optimization and development initiatives

  • Collect, analyze, and document data in accordance with established procedures and GMP/GLP best practices

  • Perform analytical characterization using methods such as UV spectroscopy, SDS-PAGE, ddPCR, ELISA, and HPLC

  • Troubleshoot purification challenges and recommend process improvements

  • Collaborate cross-functionally with upstream development, analytical, and manufacturing teams

  • Maintain laboratory equipment, prepare buffers, manage chromatography columns, and ensure compliance with safety and documentation standards

Qualifications

Required:

  • Master’s degree in Biology, Biochemistry, Chemical Engineering, Biotechnology, or related field

  • Minimum 2 years of hands-on purification experience in academic or industry settings

  • Practical experience with CsCl density gradient ultracentrifugation, ion-exchange chromatography, and affinity purification

  • Experience with buffer preparation and purification process fundamentals

  • Understanding of analytical methods for biologic or viral vector characterization

  • Strong documentation practices and attention to detail

Preferred:

  • Experience with AAV or other viral vector purification using CsCl density gradients and column chromatography

  • Experience operating AKTA systems and Unicorn software

  • Familiarity with regulated laboratory environments supporting GMP or GLP activities

Benefits

System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.



Ref: #558-Scientific


About the Company

J

Joulé

With extensive scientific, clinical, and healthcare industry experience, Joulé recruiters excel at placing talent across core specialty areas:

  • Scientific staffing for hard-to-find skills

Working across every scientific discipline, Joulé places biologists, chemists, scientists, technicians and other specialists.

  • Clinical lifecycle recruiting

From research to regulations, safety to statistics, Joulé helps clients manage every stage of the clinical development lifecycle.

  • Equipment calibration, maintenance and validation

Laboratory and facility support comes with a total quality commitment backed by ISO 9001:2008 certification.

  • National healthcare recruitment

Trust Joulé’s extensive experience in physician, advanced practice provider and executive direct placement search.

COMPANY SIZE
500 to 999 employees
INDUSTRY
Biotechnology/Pharmaceuticals
WEBSITE
https://www.jouleinc.com/