Jobs at GenScript

Leads integrated, multi-channel marketing campaigns and content strategy for ProBio's life sciences services. Owns marketing plans, customer journey mapping, value propositions, messaging, stakeholder alignment, budgets, performance measurement, and optimization. Partners with commercial, product, scientific, regional marketing, and external teams to drive awareness, engagement, pipeline, revenue, and customer experience. Presents strategies and insights to senior leadership while independently managing complex initiatives.

Supports and improves the Quality Management System for clinical and commercial cell and gene therapy products. Responsibilities include QA review of deviations, CAPAs, change controls, investigations, complaints, risk management, document control, quality metrics, management reviews, audits, and regulatory inspection readiness. The role performs root-cause analysis, monitors corrective actions, prepares quality reports, and collaborates with internal teams, customers, and external resources to maintain GxP and GMP compliance.

Leads U.S. business development for ProBio’s Discovery services, including commercial strategy, team leadership, strategic account management, pipeline growth, forecasting, customer engagement, proposal negotiation, and closing scientific service opportunities. Collaborates with technical and scientific teams to develop solutions and expand customers into downstream development and CDMO services. Represents the company at customer meetings, conferences, and industry events.

Develop and execute sales strategies across Israel, acquire and expand customer accounts, drive revenue growth, negotiate proposals and contracts, manage key relationships, ensure customer satisfaction, and maintain regulatory compliance. The role requires life sciences expertise, strong commercial and communication skills, English and Hebrew fluency, and regular customer visits.

Provides technical customer support for biotech products and services, handling inquiries, complaints, technical advice, requirements analysis, quotations, and customer solutions. Partners with sales, production, project management, marketing, logistics, and finance teams. Uses hands-on molecular biology and biochemistry expertise to advise customers, support account managers, improve satisfaction, and occasionally present at trade shows. The role is designed for a recent Master's graduate in life sciences.

Leads biologics CMC projects from proposal through completion, serving as the technical SME across cell line development, process development, GMP manufacturing, and regulatory support. Supports business development through client presentations, solution development, proposals, conferences, and client visits. Coordinates with CMC, project management, manufacturing, and commercial teams to define scope, strategy, timelines, deliverables, and successful project execution.

Supports day-to-day HR operations, employee lifecycle activities, HR data management, reporting, onboarding, contract administration, personnel records, offboarding, documentation, process improvement, and HR projects within an international team.

Develop long-term product portfolio strategies and roadmaps for life science research reagents. Identify unmet customer needs, emerging technologies, market white spaces, and competitive opportunities. Evaluate build-versus-buy-versus-partner options using scientific, commercial, IP, and economic criteria. Partner with R&D, marketing, business development, commercial, manufacturing, supply chain, and quality teams to shape innovation programs and present data-driven recommendations to executives.

Manage protein expression service projects from evaluation and proposal through execution and client updates. Coordinate scientific, commercial, and production teams, troubleshoot project issues, support technical business development, and improve service platforms based on market and competitor insights.

Contract Recruiter responsible for high-volume hiring across US sites during a 6-month contract. Screen applicants, recommend hires, and ensure compliance with EEO/ADA. Maintain recruiting processes and drive standardization while supporting general HR duties onsite in Piscataway, NJ.

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.