Jobs at GenScript

Supports protein sciences R&D projects through experimental design, literature review, mammalian cell culture, protein production and purification, and biochemical and biophysical characterization. Maintains experimental records, reports, SOPs, and laboratory information systems while supporting inventory, safety, process development, technology transfer, and cross-functional collaboration with Production, QC, and OE teams.

Conducts biotechnology research experiments involving cell culture, protein purification, protein concentration testing, SDS-PAGE, Western blotting, endotoxin testing, HPLC, and LC-MS. Analyzes experimental data, documents results, supports multiple R&D projects, maintains laboratory hygiene and equipment, replenishes supplies, and follows safety protocols and SOPs.

Manages domestic and international logistics for clinical and commercial biotech products at a GMP facility. Responsibilities include coordinating shipments, customs clearance, brokers, import and export permits, tracking, shipping and receiving, records, freight invoices, and cross-functional scheduling. The role supports cold-chain biological-material logistics, maintains compliance with QMS, cGMP, SOP, and EHS requirements, and may require physical lifting, weekend work, holidays, and overtime.

Leads marketing across the Americas and Europe, managing a regional team and annual marketing plan. Develops customer insights, value propositions, brand messaging, content, demand-generation programs, events, webinars, and ABM initiatives. Partners with Sales and global marketing teams to align go-to-market priorities, generate pipeline, track KPIs, and optimize marketing ROI. The role also ensures brand consistency, team development, stakeholder alignment, and effective regional execution.

Lead the site Environmental, Health, and Safety program for a biologics and gene therapy CDMO. Responsibilities include regulatory compliance, hazardous waste, wastewater, air emissions, biosafety, industrial hygiene, occupational health, risk assessments, incident investigations, CAPA, training, emergency response, audits, inspections, and EHS performance reporting across laboratories and GMP manufacturing operations.

Develop and maintain automation workflows for high-throughput biomanufacturing. Provide hands-on troubleshooting and maintenance for laboratory instruments and integrated automation systems, resolving mechanical, software, and system integration issues. Manage project timelines, coordinate internal resources, communicate across teams, and support technology transfer. The role requires experience with liquid-handling instruments and writing automation scripts or protocols for Tecan, Hamilton, and Thermo Momentum systems.

Develops and optimizes high-throughput sequencing library preparation workflows, including customized methods for Illumina and ONT platforms. The role analyzes and presents biological data, builds and uses bioinformatics pipelines, manages project timelines, coordinates internal resources, and supports technology transfer across teams. Candidates need a PhD in a relevant field, more than two years of scalable NGS workflow experience, programming proficiency, and strong molecular biology and microbiology expertise.

Lead the Seattle site's ISO 9001-certified Quality Management System for RUO production and R&D. Develop QMS strategy, host customer and ISO audits, manage supplier qualification and quality agreements, support tech transfer and R&D SOPs, oversee CAPA/change control/risk management, and provide cross-site quality leadership across production, QC, and engineering teams to ensure timely product release and continuous quality improvement.

Provide day-to-day office and facilities administration, vendor and stakeholder coordination, travel and event arrangements, IT asset support, compliance of administrative processes, and general support for employees, visitors, and office projects to ensure efficient operations.

Perform mammalian cell culture and protein expression experiments, operate bioreactors and centrifuges, purify recombinant proteins using chromatography, and analyze quality with Western blot and SDS-PAGE. Maintain lab equipment, document protocols/results, follow safety procedures, and collaborate with cross-functional teams.

Join GenScript's Sales Talent Community to be considered for sales and business development roles supporting gene synthesis, biologics, CDMO, and cell/gene therapy solutions. Candidates should have life-sciences sales experience, strong communication and relationship skills, and the ability to work independently in a fast-paced environment.

The Sales Account Manager will implement sales strategies to achieve sales goals, collaborate with teams, and expand business into new markets, while reporting and forecasting sales activities.

Develops and optimizes downstream purification processes for AAV and LVV viral vector manufacturing, including chromatography, TFF, viral clearance, and sterile filtration. Supports scale-up, technology transfer, cGMP risk evaluation, deviation management, regulatory CMC submissions, and manufacturing activities. The role conducts hands-on experiments, analyzes data, collaborates cross-functionally, presents project updates, and may lead a small team.

Manage daily operation, maintenance, and administration of SAP MM/WM/PP/SD. Lead rollouts and continuous improvements, ensure master data integrity and SOP compliance, gather requirements, draft functional specs, organize UT/IT/UAT testing, and track post-go-live adoption.

Coordinate QC and QA work, complete orders and troubleshoot, analyze production data, manage projects, formulate SOPs, and assist in quality monitoring.

The Automation Engineer manages the administration of automation systems, including SCADA and PLCs, ensuring compliance and system integrity through collaboration and validation processes.

The role involves developing and executing business strategies for market penetration in the EU, managing customer relationships, and leading deals in the biopharma industry.

Supports development and operation of a GMP QC microbiology laboratory for clinical manufacturing. Performs environmental monitoring, cleanroom validation, water and gas testing, bioburden, growth promotion, mycoplasma, virology, and microbial assays. Maintains compliance with cGMP, SOPs, safety standards, and GMP documentation requirements while supporting technology transfer, laboratory optimization, and daily QC activities.

Provides customer-facing technical integration support for U.S. and European commercial teams. Coordinates requirements gathering, configuration, API and data-flow testing, troubleshooting, documentation, and project activities. Reviews HTTP, authentication, XML, JSON, and integration payloads; collects diagnostic information; tracks tasks, dependencies, risks, and issues; and coordinates with customers, business teams, project managers, developers, and cross-functional teams in English and Mandarin.

The Procurement Specialist will manage procurement needs, collaborate with teams, conduct negotiations, maintain vendor relationships, and ensure compliance with procurement policies.