Field Application Scientist

GenScript

. Act as the US Regional technical liaison for GenScript’s gene and cell therapy product line .

Posted 11/9/2026full-timeRemote • United StatesMid-LevelSenior💰 $95,000 - $115,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in gene and cell therapy product lines, regulatory compliance in GMP workflows, and effective communication across diverse teams. Proven ability to manage projects, develop workflows, and provide technical training and support.

Highest-signal resume keywords

Gene And Cell Therapy ExpertiseRegulatory Compliance In GMP WorkflowsProject Management SkillsTechnical Training DeliveryStrong English Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Drug Development ProcessesBioengineeringBiochemistryCell BiologyCI Workflow ProtocolsTechnical TroubleshootingApplication Note WritingScientific Article PublicationCustomer Feedback CollectionProduct Development Feedback

Soft Skills

Interpersonal SkillsProject ManagementInnovative ThinkingMeticulous Risk ControlEffective Communication

Certifications & Qualifications

Master's Degree

Industry Keywords

BiotechPharmaCDMOGMPLife SciencesKey Opinion LeadersScientific DevelopmentsApplication Use CasesEnd-To-End SolutionsCustomer Inquiries

About the role

Key responsibilities & impact

Act as the US Regional technical liaison for GenScript’s gene and cell therapy product line
Support sales through technical calls, site visits, instrument demonstrations, customer inquiries, and opportunity conversion
Create and optimize end-to-end CI workflow protocols and validate results at customer sites or internal labs
Provide regulatory compliance expertise for products introduced into GMP workflows
Manage custom nanobead, GCT reagent, and kit projects with R&D and production; track progress and deliverables
Deliver tiered technical training for customers, internal teams, and distributors
Provide onsite and virtual troubleshooting for complex protocol, workflow, and product issues
Represent the company at conferences, workshops, and academic or industry events
Connect with key opinion leaders and business leaders and monitor scientific developments
Write, publish, and present application notes, white papers, and scientific articles
Develop joint workflows and end-to-end solutions with life sciences companies or academic groups
Maintain product knowledge and build the internal knowledge base
Provide product-development feedback to R&D and GPM
Collect and share customer feedback on application use cases and product improvements

Requirements

What you’ll need

Master’s degree with 3+ years industry experience in biotech, pharma, or CDMO, in cell and gene therapy fields
Hands-on exposure to drug development processes
Strong English communication skills, written and spoken
In-depth understanding of bioengineering, biochemistry, cell biology, and related drug development value chain
Keen industry insights to capture key product performance
Rigorous and pragmatic approach
Strong sense of responsibility and meticulous risk control
Innovative breakthrough abilities and passion for new products and technologies
Excellent interpersonal and project management skills
Ability to communicate effectively across organizations and cultures

Benefits

Comp & perks

Medical, dental, and vision insurance
401(k) retirement plan with a company match that vests fully on day one
Paid parental leave after three (3) months of employment
Paid time off including vacation time, personal time, sick time, floating holidays, and company holidays
Flexible spending and health savings accounts
Life and AD&D insurance
Short- and long-term disability coverage
Legal assistance
Supplemental pet, critical illness, accident, and hospital indemnity insurance
Commuter benefits
Well-being initiatives
Peer-to-peer recognition programs