Senior Associate Scientist, Downstream Process Development

WuXi Biologics Cayman Inc
  • Cranbury, NJ
  • $55,000–$87,000 Per Year
2 days ago

Job Description

Career Opportunities: Senior Associate Scientist, Downstream Process Development (5721)

Requisition ID 5721 - Posted 09/23/2026 - Cranbury, NJ - United States

Job Title - Senior Associate Scientist, Downstream Process Development

Work Location - Cranbury NJ

Job Summary

This role is intended for an experienced, operations-focused Downstream Scientist who can independently plan, execute, and troubleshoot downstream purification activities in support of process development, scale-up, pilot production, technology transfer, and GMP manufacturing support. The Scientist must have strong hands-on experience with downstream unit operations, including chromatography, UF/DF, TFF, viral inactivation, depth filtration, sterile filtration, buffer preparation support, and equipment setup/operation. Pilot-scale downstream processing experience is strongly preferred. The role will serve as a key technical and operational contributor, working closely with PD, manufacturing, analytical, and project teams to ensure safe, compliant, and timely execution of downstream activities.

Job Responsibilities

  • Independently plans and executes hands-on downstream purification operations from bench scale to pilot scale, including chromatography, filtration, viral inactivation, UF/DF, TFF, and related process steps to support development, scale-up, and non-GMP material generation.
  • Coordinates operational readiness for downstream runs, including equipment availability, column or membrane preparation, buffer and material readiness, batch record or protocol preparation, execution logistics, and communication with supporting functions.
  • Provides real-time process monitoring, operational troubleshooting, and technical decision-making during downstream execution; identifies process, equipment, or material risks and proposes practical mitigation actions.
  • Documents execution details, process observations, deviations, troubleshooting outcomes, and data analysis clearly and accurately in protocols, reports, batch records, logbooks, and other required documentation; supports training of cross-functional staff as needed.
  • Supports technology transfer to GMP manufacturing by providing process understanding, operational guidance, run support, deviation assessment, investigation input, and practical recommendations for manufacturing execution.
  • Serves as Downstream purification SMEs to participates in client calls and face to face meetings. Provides project plans and updates to clients.
  • Authors Downstream lab equipment SOPs; maintains equipment functionality and coordinates repairs and preventative maintenance.
  • Performs job specific tasks in compliance with applicable Regulations, International Standards, and WuXi Biologics internal policies and guidelines.
  • Completes all required training (i.e. safety, equipment etc.).
  • Contributes to the overall operations and to the achievement of departmental goals.
  • May be required to assist in other departments or assigned other duties.

Qualifications

  • PhD in Life Sciences or related field, MS with 2+ years or BS with 4+ years of experience in a biopharmaceutical or biological contract testing/manufacturing organization.
  • Demonstrated hands-on experience operating and troubleshooting downstream purification processes and equipment, including chromatography skids or systems, columns, TFF/UFDF systems, pumps, filters, tanks, mixers, single-use assemblies, and related process instrumentation.
  • Pilot-scale or manufacturing-scale downstream processing experience is strongly preferred, including hands-on run execution, scale-up support, equipment preparation, buffer and material readiness, process monitoring, and coordination with manufacturing, pilot plant, analytical, and project teams.
  • Strong oral & written communication skills are required.
  • Ability to work effectively as part of a team and to exhibit effective interpersonal skills.
  • Experience in a cGMP environment is highly desirable.
  • Ability to take on multiple tasks simultaneously.
  • Proficient in Microsoft (Excel, Word, Outlook)

The anticipated salary for this position is $55,000 - $87,000

The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertis and company business needs.

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Numbers & Facts

LocationCranbury, NJ
Salary$55,000–$87,000 Per Year

Skills

  • Analysis Skillsunmatched
  • Biologyunmatched
  • Chromatographic Systemsunmatched
  • Chromatographyunmatched
  • Communication Skillsunmatched
  • Contract Manufacturingunmatched
  • Cross-Functionalunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Data Analysisunmatched
  • Documentationunmatched
  • Equipment Maintenance/Repairunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Identify Issuesunmatched
  • Instrumentationunmatched
  • Interpersonal Skillsunmatched
  • Laboratory Equipmentunmatched
  • Logisticsunmatched
  • Maintenance Servicesunmatched
  • Manufacturingunmatched
  • Manufacturing Analysisunmatched
  • Manufacturing/Industrial Processesunmatched
  • Microsoft Excelunmatched
  • Microsoft Outlookunmatched
  • Microsoft Product Familyunmatched
  • Microsoft Wordunmatched
  • Multitaskingunmatched
  • Operations Processesunmatched
  • Pilot Plantunmatched
  • Presentation/Verbal Skillsunmatched
  • Preventative Maintenanceunmatched
  • Process Developmentunmatched
  • Process Managementunmatched
  • Project Planningunmatched
  • Pumpsunmatched
  • Regulatory Complianceunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Team Playerunmatched
  • Technical Supportunmatched
  • Time Managementunmatched
  • Time Trackingunmatched
  • Writing Skillsunmatched

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