--- title: 'Senior Scientist / Research Scientist, Molecular Biology at GenScript/ProBio' canonical: 'https://feeny.ai/job/senior-scientist-research-scientist-molecular-biology-genscript-probio-seattle-p7wbdnydqd6b' type: 'job' last_seen: '2026-11-10' --- # Senior Scientist / Research Scientist, Molecular Biology at GenScript/ProBio - **Company:** GenScript/ProBio - **Location:** Seattle, WA - **Posted:** 2026-11-05 - **Last confirmed live:** 2026-11-10 - **Apply:** https://job-boards.greenhouse.io/genscript/jobs/5285504007 ## Job description ## About GenScript Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions. Position: Senior Scientist / Research Scientist, Molecular Biology Location: Seattle, WA Reporting to: Project Lead Role Description: We are seeking a highly motivated and experienced scientist with a multidisciplinary background in molecular biology and synthetic biology, a strong product-development mindset, and the ability to build new technologies and workflows from the ground up. As a key member of a small, collaborative R&D team, this scientist will lead the development of innovative molecular biology products and technologies, with a particular focus on gene synthesis and DNA library construction using GenScript’s proprietary high-throughput DNA synthesis platforms. The role combines bench-based research, technical leadership, supervision of junior team members, and management of R&D projects from concept and feasibility assessment through process development, technology transfer, and commercialization. The successful candidate will help establish robust, scalable workflows that enable automated, large-scale production while collaborating closely with cross-functional partners in bioinformatics, chemistry, manufacturing, and quality. Key Responsibilities: - Lead bench-based research to design, develop, and optimize molecular biology products and services using GenScript’s proprietary high-throughput DNA synthesis platform. - Develop next-generation gene synthesis technologies and associated assays to simplify workflows and improve performance, quality, cost, safety, and scalability. - Lead new product and process development to expand capabilities in gene assembly, DNA library construction, next-generation cloning, and DNA amplification. - Assist to manage R&D projects from concept through technology transfer, defining project scope, experimental strategies, deliverables, timelines, resource requirements, and success criteria. Track progress, identify technical risks, and coordinate mitigation plans to support timely execution. - Supervise, mentor, and train junior scientists and research associates. Set clear objectives, guide experimental design and troubleshooting, review data and documentation, and provide regular feedback to support scientific development and accountability. - Coordinate day-to-day research activities and prioritize experimental work across assigned projects in alignment with team objectives and available resources. - Lead technology transfer to manufacturing, collaborating with manufacturing and quality teams to support successful product launches and continuous process improvement in an ISO 9001-compliant environment. - Develop and optimize automated workflows that translate research methods into robust, reproducible, and scalable production processes. - Collaborate with colleagues in bioinformatics, chemistry, and other key functions to translate research advances into competitive reagent and service offerings. - Critically evaluate experimental data, draw actionable conclusions, and communicate scientific findings, project progress, risks, and recommendations through presentations, reports, and team updates. - Author and review technical documentation, including technology transfer packages, standard operating procedures (SOPs), analytical reports, invention disclosures, and patent applications. Qualifications: Education - A degree in Biochemistry, Chemical Biology, Molecular Biology, Chemistry, Synthetic Biology, or a closely related discipline, with one of the following combinations of education and relevant industry experience: - Bachelor’s degree with at least 8 years of relevant industry experience. - Master’s degree with at least 5 years of relevant industry experience. - D. with at least 3 years of relevant industry experience. Required Qualifications - Proven track record in assay and product development, including turning research concepts into reproducible, scalable methods. - Strong knowledge of molecular biology, biochemistry, and enzymology, including DNA and RNA. Knowledge of protein synthesis, protein characterization, and affinity assays is a plus. - Hands-on expertise in nucleic acid manipulation and analysis, including primer and probe design, PCR, isothermal amplification, gene assembly, cloning, qPCR, DNA/RNA purification, and capillary electrophoresis. - Experience with next-generation sequencing (NGS) is preferred, especially for characterizing synthetic DNA and libraries. - Expertise in liquid handlers and laboratory automation, including method development, optimization, and troubleshooting. Experience with Beckman and Hamilton systems is preferred. - Experience with method verification and validation in a product-development setting. - Familiarity with automated laboratory systems and electronic documentation systems (ELN/LIMS) is preferred. - Experience transferring workflows to automated, large-scale manufacturing in an ISO 9001-compliant environment is preferred. - Ability to lead R&D projects, including setting priorities, managing timelines, and resolving technical challenges. - Experience supervising, mentoring, or guiding junior scientists or research associates. - Demonstrated success collaborating with interdisciplinary teams. - Excellent documentation and communication skills, including preparing data summaries, technical and scientific reports, and SOPs, and transferring procedures to manufacturing. - Goal-oriented, hands-on, and innovative approach to problem solving. - Self-motivated and passionate, and comfortable working in a fast-paced environment. Benefit: - Medical Insurance/ Vision Insurance/ Dental Insurance - 401(k) & Retirement Savings Plan (RSP) - Short Term Disability Insurance - New Child Leave - Paid Time Off - Paid Company Holidays per year - Paid Sick Days (earned based on hours worked) - Compassionate Leave - Jury Duty Leave - Float day - Personal days Perks: - Free colleague meals during shift - Onsite gyms Compensation: Salary range: $120,000 – $160,000 total compensation, including bonus, depending on experience and qualifications. Benefits: Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work. GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform. ## About GenScript/ProBio ## Company Overview - **One-liner**: GenScript Biotech Corporation, through its subsidiary ProBio, provides end-to-end contract development and manufacturing (CDMO) services for biologics, cell and gene therapies, and mRNA innovations, accelerating drug development from discovery to commercialization. - **Entity Type**: Public (Hong Kong Stock Exchange: 1548.HK) - **Headquarters**: Piscataway, New Jersey, United States (GenScript HQ); ProBio’s U.S. CDMO center of excellence in Hopewell, New Jersey - **Founded**: 2002 (GenScript) - **Founders**: Not publicly listed on provided sources; GenScript was founded by a team of scientists and entrepreneurs. ## Core Business - **Primary industry/industries**: Biotechnology – Contract Development and Manufacturing Organization (CDMO); Life Science CRO; Cell & Gene Therapy; Biologics; mRNA therapeutics. - **Target customers**: Biotech and pharmaceutical companies of all sizes (startups to large pharma), academic researchers, and clinical-stage developers – B2B focused. - **Mission or purpose statement**: “Make People and Nature Healthier Through Biotechnology” (GenScript); ProBio’s mission: “Through our commitment to quality, collaboration and innovation, ProBio delivers customized solutions to transform scientific discoveries into market-ready therapies that make a lasting impact on patients’ health and well-being.” ## Products & Services - **Plasmid DNA Development & GMP Manufacturing**: Specialized services for cell and gene therapy programs, from early development through clinical and commercial supply, manufactured at the Hopewell, New Jersey facility (FDA-compliant). - **Viral Vector Development & GMP Manufacturing**: End-to-end support for AAV, lentivirus, and other vectors for clinical and commercial programs. - **mRNA Development & Manufacturing**: Integrated solutions for speed, scalability, and quality, covering process development and GMP production. - **Biologics Discovery & Development**: Antibody discovery, engineering, cell line development, upstream/downstream processing, and drug product manufacturing for monoclonal, bispecific, and multi-specific antibodies and recombinant proteins. - **CMC Services for CGT**: Full CMC support for plasmids, viral vectors, mRNA, and nucleic acid drugs – from IND filing to commercial manufacturing, including cell banking, process characterization, analytical development, and stability studies. - **Integrated Services**: Process development, bioanalytical development, formulation, and in vitro/in vivo pharmacology. ## Market Standing - **Valuation/Market Cap**: Not publicly available from provided sources (GenScript is a public company with ticker 1548.HK; market cap varies – check financial platforms for latest). - **Key Metric**: GenScript employs approximately 6,165 people and has served over 200,000 customers across more than 100 countries. ProBio has helped customers obtain more than 150 IND approvals since October 2017. - **Notable Investors/Partners**: GenScript is a publicly traded company; ProBio is a wholly owned subsidiary. No specific investor names provided. Key partners include biotech and pharma companies globally. - **Growth Signals**: Global expansion with facilities in the US, Netherlands, South Korea, and China (Hong Kong, Shanghai, Nanjing). GMP capacity meeting FDA, EMA, and NMPA regulatory standards. Growing network of development and manufacturing sites to support international programs. ## Competitive Advantages - **End-to-End Platform**: ProBio offers a fully integrated “DNA-to-GMP” platform covering discovery, development, and manufacturing across multiple modalities (plasmids, viral vectors, mRNA, antibodies) – reducing handoffs and risk. - **Regulatory Expertise**: Facilities designed to meet FDA, EMA, and NMPA requirements, enabling clients to navigate global submissions. - **Proprietary Technology**: Technology-driven platform processes that minimize variability and accelerate timelines from early development to commercial supply. - **Proven Track Record**: 150+ IND approvals since 2017 and partnerships with companies of all sizes demonstrate reliability and depth. ## Strategic Focus - **Current priorities and direction for growth**: Expand global footprint to be closer to customers and align with regional regulatory needs; invest in cutting-edge capabilities for advanced therapies (CGT, mRNA); maintain a customer-centric, innovation-driven culture to accelerate client programs. - **Key initiatives**: Building out purpose-built facilities for each modality, enhancing proprietary platform processes, and recruiting talent across R&D, manufacturing, and business development. ## Why Work Here - **Culture highlights**: Mission-driven environment focused on “making people and nature healthier.” Core values: Customer Centric, Innovation, and Integrity. Emphasis on ethical standards, transparency, and collaboration. - **Remote/hybrid/office policy**: Not explicitly stated in provided sources; roles appear to be based at specific sites (e.g., Hopewell, NJ; Piscataway, NJ; Europe; Asia). Some positions (e.g., Commercial Technical Support Specialist) offer remote in Europe. - **Notable perks or engineering culture**: Opportunity to work on cutting-edge therapies (gene editing, mRNA, biologics) that directly impact patient health. Global career opportunities across multiple continents. The company encourages “new ideas and challenging traditional approaches” – a strong innovation culture for scientists and engineers. ## Sources 1. [genscriptprobio.com](https://genscriptprobio.com/about-us.html?src=fromgenscriptsubpage) 2. [genscript.com](https://www.genscript.com/our-business.html) 3. [probiocdmo.com](https://www.probiocdmo.com/careers.html) 4. 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