GenScript jobs - 40 jobs

GenScript is the leading gene, peptide, protein and antibody research partner for fundamental life science research, translational biomedical research, and early stage pharmaceutical development. Since our establishment in 2002, GenScript has exponentially grown to become a global leading biotech company that provides life sciences services and products to scientists over 100 countries worldwide. During our tenure we have built the best-in-class capacity and capability for biological research services encompassing gene synthesis and molecular biology, peptide synthesis, custom antibodies, protein expression, antibody and protein engineering, and in vitro and in vivo pharmacology - all with the goal to Make Research Easy. Life Sciences Research Services Life Sciences Research Catalog Products Preclinical Drug Development Services Industrial Synthetic Biology Products Key Facts about GenScript Peer-Reviewed Citations - GenScript is the frequently cited biotech company in the world. More than 12,000 papers cite the service and products from GenScript. Gene synthesis - one of the largest gene synthesis capacity in the world with > 100 million bp/month; record length 50 kb; turnaround time as short as 4 business days. Peptide synthesis - 6,000/month; record length over 100 aa. Antibody services - 6,000 rabbits and 12,000 rodents; pAb/mAb in 45 days; guaranteed immune response & amount. Protein expression - 4 major expression systems (bacterial, mammalian, yeast, insect); guaranteed purified protein. Animal model services - 4 key in vivo pharmacological services: in vivo drug efficacy evaluation, pharmacokinetic studies, toxicity assessment, and biomarker & bioanalysis services. Job Description Responsible for importing and exporting raw materials domestically and internationally · Responsible for loading/unloading products/materials Coordinate with Shipping Department for orders by picking/tracking products based on client request Responsible for updating/tracking packages by using internal ordering system · Responsible for shipments from internal customers Manage Inventory by keeping inventory neat and organized and annual/quarter cycle count Other relevant projects and duties assigned by management Qualifications · Minimum high school diploma. Associate's or above degree in Supply Chain or relevant field is a big plus can-do attitude and a willingness to learn and meet the demands of our customers and management Computer literate. Familiar with Microsoft office system, including Outlook, Excel, Word, and PPT Able to lift up to 50 pounds with or without reasonable accommodation Good command of the English and Mandarin language verbally and written Able to work independently and collaboratively with team members Flexible for occasional overtime opportunities Work experience in Warehouse is a big plus Additional Information GenScript USA 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 GenScript'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. maintains a drug-free workplace.

About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Scope: GenScript is seeking a Corporate Communications Manager, International, to support the Integrated Communications & Content department. Reporting to: Director of Integrated Communications & Content Location: Remote- United States The estimated salary range is $100,000 - $130,000, based on experience level. Key Responsibilities: * Develop GenScript BioTech Corporation's corporate brand image and ensure that it's unified across international markets. * Develop and execute high-impact, integrated global corporate communication strategies and narratives with a focus on all international markets (excluding China) that align with the company's corporate brand image, goals and values. * Implement end-to-end corporate communications plans for company milestones, corporate commitment and employee brand campaigns, ESG and sustainability programs, leveraging earned media, sponsored content, social media, influencer relations, and owned media channels to engage key external audiences. * Strategize and implement brand PR, including product launches, strategic partnerships, funding announcements, and issues management, with differentiated strategies tailored to the relevant media environment for the region. * Serve as media relations expert by building and maintaining relationships with key journalists and media outlets, writing press bulletins and developing pitch angles with the goal of delivering thoughtful, positive news coverage. * Developing and executing plans to manage the company's reputation during adverse situations. * Monitor market sentiment in media and social platforms (X/Twitter, Reddit, LinkedIn), providing timely risk alerts and crisis response. * Collaborate cross-functionally with Marketing, Legal, Investor Relations, HR teams, regional counterparts and other internal stakeholders to ensure successful execution and consistent tone/messaging of corporate communications initiatives. * Effectively manage PR agency and content production partner relationships and budgets to ensure delivery of their support through clear objectives, KPIs, continued drive for excellence and innovation. * Stay informed on evolving regulations and narrative expectations (e.g., ESG, climate, biotech policy). * Develop and measure effective metrics/KPIs to track communication impact and deliver the best business outcomes. Qualifications: * Bachelor's degree or above in Communications, Journalism, Marketing, International Relations, or related fields. * Minimum 5 years of PR or corporate communications experience with demonstrable measures of success; at least 3 years of experience in the US market preferred. * Strong knowledge of the international media ecosystem, communication habits, and public opinion environment, with proven success in pitching and securing coverage in media. * Experience in translating scientific/technical content for a broad range of audiences. Pharmaceutical/biotech or healthcare experience preferred. * Excellent written/verbal communication and presentations skills in English, with professional proficiency in writing press releases, media pitches, and executive speeches; ability to negotiate and persuade. * Understanding of the biotechnology industry and/or experience in a high-growth company PR is preferred. * Strong crisis management awareness and ability to respond quickly with effective solutions for overseas media issues. * Effective stakeholder management and ability to work in a highly matrixed organization and across geographical boundaries. * Global perspective and cross-cultural communication skills, with flexibility to adapt to diverse market needs. * Proactive, adaptable, highly organized, and capable of leading multiple projects efficiently under pressure. #LI-EB1 #GS 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 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Title: Procurement Specialist, Direct Materials Location: Piscataway, NJ or Redmond, WA Employment Status: Full Time Reports to: Senior Procurement Manager Role Description This role will support the end-to-end sourcing and procurement of direct materials and consumables to support production. Key duties include ensuring daily operations meet SLA and KPI targets, overseeing material planning for critical items, and driving strategic sourcing initiatives. The candidate will manage vendor relationships, negotiate contracts, and identify cost-saving opportunities through category management and market analysis. Close collaboration with cross-functional teams is essential to ensure supply continuity, compliance with quality and regulatory standards, and readiness for audit requirements. The estimated salary range is $60,000 - $70,000, based on experience. Job Responsibilities: * Oversee material planning for Green Channel item replenishment to meet inventory KPIs while ensuring continuity of supply. * Lead strategic sourcing and manage the procurement process for direct materials and consumables used in production, ensuring alignment with cost objectives, quality standards, and regulatory requirements. * Develop alternative vendors for critical materials and components to ensure supply continuity and mitigate supply chain risks. * Conduct category management to identify cost-saving opportunities through vendor consolidation and the use of alternative materials or components. * Leverage negotiation, analytical, and market research skills to drive value through cost reduction initiatives. Track and report KPIs related to cost savings, cost avoidance, on-time delivery (OTD), and efficiency improvements. * Execute vendor management by building supplier profiles, conducting regular business reviews, and securing both short- and long-term pricing contracts and Master Supply Agreements (MSAs). * Serve as the primary point of contact for negotiating and executing contracts and agreements in coordination with the legal team. * Collaborate closely with production team to provide effective procurement support by understanding production processes, tracking changes in material consumption, and proactively addressing critical issues with urgency. * Maintain active communication with suppliers of critical materials to stay updated on market conditions, ensure timely deliveries, and identify potential risks and opportunities. * Work cross-functionally with quality, finance, and other departments to ensure procurement processes remain compliant with company policies and regulatory standards. * Respond to internal and external audit challenges by providing complete and accurate procurement documentation and justifications. Qualifications: * Bachelor's degree or higher in Business, Supply Chain Management, or a related field * Minimum of 1-3 years of experience in procurement, with a focus on direct materials * Strong negotiation, communication, and analytical skills * Project management skills, with experience in procurement for lab projects preferred; this experience will be considered a significant advantage * Proven capability to navigate a dynamic, fast-paced environment while adapting to shifting priorities and identifying opportunities #LI-EB1 #GS 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 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Position Overview： The position reports to the Associate Director, Downstream Viral Vector Process Development & MSAT Department. This role is ideally suited for a dynamic bench-focused individual to support/lead translation of research process to GMP-compliant manufacturing, and will develop, scale-up, and evaluate the technology transfer of viral vector processes. This is a great opportunity to join a fast-paced company, develop, and expand technical expertise to lead by example and potentially lead a small team in the near future. * Hands-on experimental work in the development and optimization of downstream unit operations (TFF, Affinity/Ion Exchange/multimodal Chromatography, Viral clearance, Sterile filtration, etc.) for viral vector manufacturing process. * Contribute to the planning, design, and execution of AAV/LVV purification-related experiments to analyze, interpret, and report data summary packages. * Interact and collaborate with internal/external partnerships to evaluate and implement new bioprocessing technologies and strategies. * Interact with cross functional teams (Analytic team, MFG, Supply chain, Facility, QA, QC) to support process technology transfer, cGMP risk evaluation, and deviation management. * Maintain and follow detailed and comprehensive project timelines. * Support in the preparation of CMC sections for regulatory submissions (IND, Annual Reports, and BLA), invention disclosures, progress reports, and publications. * Present updates to project or upper management teams on process development and manufacturing support activities. * Read and understand scientific literature in gene and cell therapy. Use the knowledge to generate ideas and contribute to process design and development. * Perform other duties as assigned based on business needs. Qualifications: * Bachelor's degree with 3-7 years, or Master's or Ph.D. degree with 1-3 years' relevant industry experience in Chemical/Biochemical Engineering, Biological Sciences, or a related scientific discipline in biotech development with particular experience in gene and cell therapy product design. Experience with LVV and AAV process development is a plus. * Previous experience in viral vector process development and manufacturing is highly preferred. * Strong understanding of process scale-up and scale-down modeling. * Good understanding of Design of Experiment (DOE) and statistical analysis. * Experience in CMC regulatory affairs for FDA, and EMA is a plus. * Strong organizational skills and detailed documentation abilities are required. * Work independently in hands-on laboratory setting, self-motivated to learn and develop new techniques. * Strong interpersonal, verbal, and written communication skills. * Results oriented, be able to effectively prioritize and complete tasks on time. * Collaboration and teamwork. * Must be comfortable in a fast-paced, multi-tasking biotech environment. Compensation: The salary range, dependent upon experience level, is $80,000 - $110,000 annually. #LW #PB 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 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Overview: We are seeking a proactive and experienced EHS Manager to oversee all environmental, health, and safety activities at our Piscataway, New Jersey site. This position will be responsible for developing, implementing, and managing site-specific EHS programs and ensuring compliance with local, state, and federal regulations. The ideal candidate will have strong experience in construction project support, including providing EHS input during early design and planning phases. The estimated salary range is $115,000 - $120,000, depending on the individuals experience and background. This position is based fully onsite in Piscataway, NJ. Responsibilities: * Lead and manage all EHS compliance activities and initiatives for the site. * Provide EHS input into facility design, equipment layout, utility planning, and construction execution from concept through commissioning. * Collaborate with engineering, construction, and facility teams during the design and construction phases to identify and mitigate safety and environmental risks. * Ensure compliance with OSHA, EPA, and other applicable regulatory agencies. * Conduct risk assessments, hazard analyses (e.g., JHA, HAZOP), and support design reviews with EHS controls in mind. * Manage incident investigation, root cause analysis, and corrective action implementation. * Develop and deliver EHS training programs for site staff, contractors, and project teams. * Support permit applications and regulatory reporting. * Lead site inspections, audits, and emergency drills. * Serve as a liaison with regulatory bodies and external contractors/vendors. * Drive continuous improvement in site EHS culture and performance. Required Qualifications: * Bachelor's degree in Environmental Science, Occupational Health and Safety, Engineering, or related field. * 5+ years of relevant EHS experience, preferably in construction, facility startup, or manufacturing environments. * Strong knowledge of OSHA, EPA, and other federal/state/local EHS regulations. * Demonstrated experience providing EHS guidance during early design and construction phases. * Ability to read and interpret engineering drawings and construction documents. * Excellent communication, training, and leadership skills. * Certified Safety Professional (CSP), Certified Industrial Hygienist (CIH), or similar certifications a plus. * Proficient in MS Office and EHS management systems Preferred Qualifications: * Experience in biotech, pharmaceutical, or high-tech industries. * Familiarity with construction safety (e.g., NFPA, ANSI standards, contractor safety management). * Experience managing EHS programs during facility commissioning/startup phases. We're Looking For Someone Who: * Builds systems, not just reacts to problems - you design processes that prevent recurring issues. * Thinks like an owner - proactive, reliable, and focused on long-term outcomes. * Leads with clarity and empathy - your team knows where they're going and feel supported. * Communicates across levels - from technician to senior leadership, you know how to align on objectives. Benefits * Competitive salary with performance-based bonuses. * Comprehensive health, dental, and vision insurance. * 401(k) retirement plan with company match. * Paid time off (PTO) and holidays. * Professional development and training opportunities. #GS #LI-EB1 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 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Scope: The Sr. Facilities Technician will be responsible for ensuring the optimal performance, safety, and reliability of all building infrastructure and systems. This role requires deep expertise in HVAC systems, electrical systems, and plumbing, along with strong proficiency in Building Automation Systems (BAS) and Building Maintenance Systems (BMS). Essential responsibilities: * Responsible for maintaining, monitoring, and performing preventive maintenance and continuous operation of all data center systems to maintain 100% Up-time including: fire/life safety, mechanical systems such as (HVAC, BAS, chillers, CRAC, CRAH, plumbing, controls), electrical including emergency backup systems such as (lighting, UPS, ATS, STS, PDU, generators, primary switchgear, power distribution, transformers), and hot water systems. * Monitors operation, adjusts, and maintains refrigeration, chilled water, and air conditioning equipment; boilers, and ventilating and water heaters; pumps, valves, piping, and filters; other mechanical and electrical equipment. Must record readings and make adjustments where necessary to ensure proper operation of equipment. Monitor building management systems and respond to alarms and alerts promptly * Requires the ability to analyze the operation of various systems, determine the cause of any problems/malfunctions and take corrective action as required * Comply with departmental policy for the safe storage, usage, and disposal of hazardous materials. Maintains a clean and safe workplace. * Learn and understand the data center site in-order to manage incidents and events that put the critical systems at risk. * Work order management, including CMMS, Vendor Management, and Customer Facing Tickets. * Understanding and complying with emergency escalation procedures. * Perform advanced troubleshooting, repair, and maintenance of HVAC, electrical, and plumbing systems. * Operate, monitor, and optimize Building Automation Systems (BAS) and Building Maintenance Systems (BMS). * Conduct routine inspections and preventive maintenance on all facility systems and equipment. * Interpret blueprints, schematics, and technical manuals to diagnose and resolve complex issues. * Collaborate with vendors, contractors, and internal teams for system upgrades and repairs. * Maintain accurate records of maintenance activities, system performance, and compliance documentation. * Ensure all work complies with local, state, and federal regulations and safety standards. * Respond to emergency maintenance requests and participate in on-call rotation as needed. * Perform additional job duties as required Basic Qualifications: * High School Diploma (or GED) with a minimum 5 years of hands-on experience in HVAC, electrical, and plumbing systems. * Proven experience with Building Automation Systems (e.g., Siemens, Johnson Controls, Honeywell). * Strong understanding of mechanical, electrical, and plumbing (MEP) systems in commercial or industrial settings. * Certification in HVAC (EPA Universal), Electrical (Journeyman or Master), or plumbing preferred * Familiarity with energy management systems and sustainability practices is a plus. * Ability to lift up to 50 lbs. and work in confined spaces, heights, and varying environmental conditions. * Must be able to stand, walk, bend, and climb ladders for extended periods * Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. * Excellent problem-solving skills and attention to detail. * Strong communication and organizational skills. * Ability to read, analyze, and interpret technical procedures, or governmental regulations and codes. * Ability to write routine reports and correspondence. * Ability to work holidays and varying shift times/hours if required * Must be able to respond to site emergencies Please note that this role is based fully onsite in Pennington, New Jersey. The estimated salary range is $92,000 - $102,000 annually. #MR #LW #PB 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.

GenScript Biotech Corporation is a leading Contract Research Organization and the world leader in biotechnology reagent service industry, as well as an open platform for pre-clinical drug discovery and pharmaceutical development, located in Piscataway, New Jersey. Our core business is in life science research, products and sevices. We are driven by innovative technologies, providing services including gene synthesis, custom protein and antibody services, and antibody, protein and catalog products. As a public company (HK Stock: 01548), our mission is to make human and nature healthier through biotechnology. Established in 2002, we have built our commercial and production centers in New Jersey, United States and Nanjing, China. More than 13,000 peer-reviewed journal articles have cited GenScript's services and products. There are also branches in Ireland, Netherlands, and Japan. We have been serving more than 100 countries and 200,000+ customers around the world for more than 16 years. For more details, welcome to visit our website ***************** Job Description Technical Account Manager provides account management and high-level technical support to customers, serving as the primary technical source for supporting sales/marketing activities. Supported by Technical Account Associates, Technical Account Managers take full responsibility of the daily operation of customer service function to strengthen customer relationships and ensure customer satisfaction. The focus of work is in project management, project design, and proactive account management. Responsibilities: 1. Provide primary business, technical and product/service advice to customers, include providing effective solutions to customer's project inquiries and generating price quotes for project design. 2. Analyze customers' needs, resolve customers' troubleshooting and/or complaints with a technical issue and advise them of additional services and product solutions when necessary. 3. Identify potential areas of concern for customers. Make recommendations based on recognizing customers' current and future needs during continued business relationship. 4. Maintain close communication with customers as well as facilitate communication with technical support when necessary. 5. Collaborate with internal teams/departments to achieve sustainable growth. 6. Organize and provide training for internal sales and external distributors by delivering presentations or/and demos. 7. Demonstrate technical expertise when attending trade shows or exhibitions. Qualifications 1. Master degree in relevant life science discipline is preferred, such as cell biology, immunology, molecular biology and peptide therapeutics. Bachelor degree is required. 2. Exceptional verbal and written communication and presentation skills. 3. Must be customer-centered and proactive/action-oriented. 4. Excellent analytical skills & problem solving skills, able to grasp new concepts quickly. 5. Strong organization skills with great attention to detail. 5. Enjoy working in a fast-paced and team-oriented environment.

About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Overview: The Laboratory Supervisor is responsible for overseeing and guiding the daily operations of the laboratory, ensuring that the work is conducted efficiently and accurately. This position requires a background in laboratory studies or work and extensive team management experience. The candidate should be able to set and break down team goals, establish employee performance assessment criteria (PBC/KPI), and drive the team towards achieving its objectives. This role has an estimated salary range of $80,000 - $90,000 dependent upon experience. Key Responsibilities: Team Management: * Lead and manage the laboratory team, assign tasks, and monitor progress. * Set annual and quarterly team goals and break them down into actionable tasks. * Conduct employee performance evaluations, set PBC/KPI, ensuring alignment of employee goals with team objectives. Communication and Coordination: * Maintain open communication channels, regularly communicate with team members, and provide feedback and guidance. * Resolve internal team conflicts and issues, fostering a positive work environment. * Coordinate with other departments to ensure laboratory work aligns with organizational objectives. Employee Development: * Identify training and development needs of employees, develop and implement training plans. * Mentor and cultivate employees, helping them improve skills and advance their careers. * Support employee career growth through regular performance evaluations. Lean Management and Site Management: * Apply lean principles to optimize laboratory processes, enhancing efficiency and quality. * Implement site management practices to ensure effective use of laboratory equipment and resources. * Monitor laboratory safety and compliance, ensuring adherence to relevant standards and regulations. Development and Improvement of SOP (Standard Operating Procedures): * Develop and maintain laboratory SOPs, ensuring all operations comply with industry best practices and regulatory requirements. * Regularly review and update SOPs to adapt to new technologies and methods. * Ensure team members are familiar with and follow SOPs, providing necessary training. Problem Analysis and Resolution: * Apply comprehensive thinking to analyze problems from perspectives such as personnel, equipment, materials, methods, and environment. * Identify potential issues and develop preventive measures to reduce impacts on laboratory operations. * Implement solutions and monitor their effectiveness to ensure problems are effectively resolved. Goal Achievement: * Represent the team in developing and executing strategies to achieve laboratory goals. * Monitor project progress, make necessary adjustments to ensure goals are met. * Regularly report team performance and project progress, providing improvement suggestions. Qualifications: * Possess a degree in a relevant field and laboratory work experience. * Extensive team management experience with the ability to set and achieve goals. * Familiarity with lean management principles and site management practices. * Excellent communication and coordination skills, able to effectively resolve issues. * Ability to mentor and develop employees, supporting the team's continuous growth. #GS 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.

GenScript Biotech Corporation is a leading Contract Research Organization and the world leader in biotechnology reagent service industry, as well as an open platform for pre-clinical drug discovery and pharmaceutical development, located in Piscataway, New Jersey. Our core business is in life science research, products and sevices. We are driven by innovative technologies, providing services including gene synthesis, custom protein and antibody services, and antibody, protein and catalog products. As a public company (HK Stock: 01548), our mission is to make human and nature healthier through biotechnology. Established in 2002, we have built our commercial and production centers in New Jersey, United States and Nanjing, China. More than 13,000 peer-reviewed journal articles have cited GenScript's services and products. There are also branches in Ireland, Netherlands, and Japan. We have been serving more than 100 countries and 200,000+ customers around the world for more than 16 years. For more details, welcome to visit our website ***************** Job Description Job Scope Key Responsibilities (in progressive tense, no punctuation mark after each sentence) · Develop and implement strategic marketing plans to achieve company objectives for Reagent Service Business Unit, through different channels: events, editors, third-party advertising, social media · Conduct channel research in areas such as effectiveness and competitor intelligence · Write and edit marketing materials, including but not limited to campaign emails, event brochures and flyers, webpages, news releases, social media posts · Support exhibitions and events, including but not limited to registration, ordering services, packing/unpacking, shipping, lead management, budget, and expense tracking · Booth layout and design, booth vendor selection and negotiation · Attend selected tradeshows · Manage marketing gift inventory · Supply other teams with requested Marketing collaterals and gifts Qualifications Experiences & Skills (no punctuation mark after each sentence) · Master's degree in Life Science · Good technical knowledge of molecular biology, synthetic biology, protein or antibody is preferred · Previous sales or marketing work experience is a big plus. · Proficient technical writing skills. · Quick learner, self-motivated, and a team player · Proficient in Microsoft Word, Excel, PowerPoint · Ability to lift 25 lbs · Ability and willingness to travel (up to 20%) Additional Information GenScript USA 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 GenScript'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. maintains a drug-free workplace.

GenScript Biotech Corporation is a leading Contract Research Organization and the world leader in biotechnology reagent service industry, as well as an open platform for pre-clinical drug discovery and pharmaceutical development, located in Piscataway, New Jersey. Our core business is in life science research, products and sevices. We are driven by innovative technologies, providing services including gene synthesis, custom protein and antibody services, and antibody, protein and catalog products. As a public company (HK Stock: 01548), our mission is to make human and nature healthier through biotechnology. Established in 2002, we have built our commercial and production centers in New Jersey, United States and Nanjing, China. More than 13,000 peer-reviewed journal articles have cited GenScript's services and products. There are also branches in Ireland, Netherlands, and Japan. We have been serving more than 100 countries and 200,000+ customers around the world for more than 16 years. For more details, welcome to visit our website ***************** . Job Description Role Overview: GenScript USA Inc. is looking for a full-time HR Intern to perform various administrative tasks and support our HR department's daily activities, including but not limited to payroll, recruiting, and employee relations and organizing and coordinating HR policies and procedures. The intern will have the opportunity to thrive in a fast-paced, strategic environment where bold, innovative thinking is welcomed and encouraged. Our rapid growth strategy means plenty of stretch assignments and opportunities to learn and grow in a fast-paced environment. Major Responsibilities: · Update our internal databases with new employee information, including contact details and employment forms · Screen resumes and application forms; schedule, confirm and set up interviews with candidates and coordinate new hire orientations · Post, update and remove job ads from job boards, careers pages and social networks · Recommend and implement personnel policies and procedures; help to prepare and maintain handbook on policies and procedures · Assist in developing presentations on metrics, reports and analysis · Perform other duties as assigned Qualifications Key Capabilities, Knowledge, and Skills: Bachelor's or Associate's degree in human resources and other relevant disciplines Able to work on a full-time basis (40 hours per week) Previous experience in administration/customer service/human resources is a plus Familiarity with HRIS, ATS and resume databases Good understanding of full-cycle recruiting Excellent written and verbal communication skills Strong organizational skills with the ability to multi-task Additional Information All your information will be kept confidential according to EEO guidelines.

About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Scope: The Sr. Global Product Manager, Gene Solutions is responsible for managing the key product line services of the Molecular Biology business. This role will be responsible for leading key NPI projects from concept through launch phase, gather customer feedback and market intelligence, and managing product lifecycle and pricing. Reporting to: Director of Global Product Management, Gene Solutions Location: US Remote (New Jersey preferred) The estimated salary range is $85,000 - $125,000, based on experience level. Key Responsibilities: * Lead NPI project with linear solution for Antibody Expression from concept phase to successful launch * Drive VoC and conduct market research to identify unmet needs, shape product requirements, and develop launch positioning & strategy * Manage product lifecycle including P&L, market analysis, product roadmap & strategy, pricing review, process optimization, and internal system upgrades * Enable global commercial teams with training, tools, and on-market support * Collaborate with Marketing to develop GTM strategy and create marketing collateral * Partner closely with R&D and Production to build new capabilities, resolve issues, and enhance existing services through customer feedback and market insights Qualifications: * Bachelor of Science degree in life sciences or related discipline is required * Master of Science or PhD degrees in life sciences preferred; MBA is a plus * 3-7 years' experience in Product Management roles in the life sciences industry * Proven track record leading successful NPI projects and developing business cases * Strong experience conducting VoC and market research * Outstanding written and verbal communication skills are required * Preferred Knowledge of molecular biology service market * Experience working with CRO is a plus * Preferred Mandarin Chinese proficiency #LI-EB1 #GS 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.

GenScript Biotech Corporation is a leading Contract Research Organization and the world leader in biotechnology reagent service industry, as well as an open platform for pre-clinical drug discovery and pharmaceutical development, located in Piscataway, New Jersey. Our core business is in life science research, products and sevices. We are driven by innovative technologies, providing services including gene synthesis, custom protein and antibody services, and antibody, protein and catalog products. As a public company (HK Stock: 01548), our mission is to make human and nature healthier through biotechnology. Established in 2002, we have built our commercial and production centers in New Jersey, United States and Nanjing, China. More than 13,000 peer-reviewed journal articles have cited GenScript's services and products. There are also branches in Ireland, Netherlands, and Japan. We have been serving more than 100 countries and 200,000+ customers around the world for more than 16 years. For more details, welcome to visit our website ***************** Job Description Coordinate office activities and operations to secure efficiency and compliance to company policies Maintain facilities management, including space planning/design, vendor contracts and relations, and facilitation of all office functions and services Ensure the smooth operation of the lunch program and snack stations, including, but are not limited to creating menus, quoting vendors, placing orders, and resolving employee complaints Maintain a professional work environment according to 5S standard Maintain office efficiency arranging necessary repairs, coordinate all office related projects to ensure office building security Act as primary liaison between the company, staff, and office building management, providing information, answering questions, and responding to requests Assist with billing by preparing and sending invoices; maintain client databases; track accounts; oversee the invoice workflow, and assist in copying and distributing production orders and other internal documents as requested Assist EHS Coordinator in establishing compliance system to meet EHS / OSHA standards Office supplies management ( track & record inventory, and make ordering requests ) Respond to emergency calls in a timely manner Assist colleagues whenever necessary Qualifications Associate degree required (Bachelor's degree preferred) Good communication skills in both English and Chinese 2+ years' experience working in an office setting Proficient in MS office and MS Excel Working knowledge in project management Ability to multi-tasking and prioritizing Must be able to lift boxes weighing 20 lbs Abnormal work hours (night time, weekends) may be required as special business needs occur Additional Information All your information will be kept confidential according to EEO guidelines.

GenScript Biotech Corporation is a leading Contract Research Organization and the world leader in biotechnology reagent service industry, as well as an open platform for pre-clinical drug discovery and pharmaceutical development, located in Piscataway, New Jersey. Our core business is in life science research, products and sevices. We are driven by innovative technologies, providing services including gene synthesis, custom protein and antibody services, and antibody, protein and catalog products. As a public company (HK Stock: 01548), our mission is to make human and nature healthier through biotechnology. Established in 2002, we have built our commercial and production centers in New Jersey, United States and Nanjing, China. More than 13,000 peer-reviewed journal articles have cited GenScript's services and products. There are also branches in Ireland, Netherlands, and Japan. We have been serving more than 100 countries and 200,000+ customers around the world for more than 16 years. For more details, welcome to visit our website ***************** Legend Biotech USA Inc. is an emerging company focusing on the development of the best-in-class immunotherapy technology for cancer cure. Teamed up with outstanding immunologists and molecular biologists, Legend has generated a strong pipeline of Chimeric Antigen Receptor (CAR) product candidates to treat a wide variety of liquid and solid tumors. Legend Biotech USA Inc. is founded on the vision that the previous incurable previous incurable cancer will be safely and effectively treated with fine-tuning products generated on our innovative technology platform. Legend Biotech is a subsidiary of Genscript. Genscript and Legend will share all back-end operations (Finance, Administrative, HR) through a transition period as Legend Biotech becomes an independent biotech. They have sites in Nanjing, China and Piscataway, NJ. Legend Biotech currently has about 100 employees. Job Description Assist Lab manager improving current plasmid prep protocol and procedure Check stocks of required consumables enabling DNA preps (Plasmid preparation kits) Transfer of solvent and solid waste to appropriate collection containers as indicated per SOP Identify and report quality or compliance concerns to management and quality function and take immediate actions to remedy Maintain lab cleanness Basic laboratory projects, and administrative tasks assigned Qualifications MS or above in Biology or related science discipline, Ph.D. research experience is a big plus 2+ years industry experience working in plasmid prep production line Strong communication, organizational, and time management skills Additional Information Knowledge of large scale automation process Experience of Large scale plasmid preps, including midi, maxi, mega and gigaprep Familiar with Molecular Biology production; Transformations, colony picking, bacterial culture, and DNA quantification using instrumentation Knowledge of Development, maintenance and full adherence All your information will be kept confidential according to EEO guidelines.

About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. We are seeking a Warehouse Data Operations Specialist to perform on-site warehouse operations and data management functions under departmental SOPs and supervisor guidance. This role requires dual expertise in modern warehouse data systems and hands-on operational skills, optimizing receiving, issuing, and inventory processes to drive departmental digitalization, visualization, and data-driven development. Location: Piscataway, NJ Employment Status: Full Time Reports to: Warehouse Manager The estimated salary range is $60,000 - $65,000, based on experience. Job Responsibilities: * Execute daily SAP/WMS system operations for raw materials and finished goods (inbound/outbound). * On-site coordination: Monitor warehouse activities, ensuring alignment between physical operations and system data. * Troubleshoot and document operational/data discrepancies; provide structured feedback. * Maintain and audit SAP/WMS master data. * Organize and archive physical/electronic documentation for compliance. * Generate and analyze warehouse KPIs (daily/monthly reports on inventory accuracy, turnaround time, etc.). * Act as a liaison between warehouse teams and production departments for urgent material requests. * Participate in cycle counts and year-end inventories; reconcile system vs. physical stock. Qualifications: Education & Experience: * Associate degree or higher in Logistics, Supply Chain, or related field. * 2+ years in warehouse data operations (manufacturing/biopharma preferred). * Dual competency: Proven experience in both system management (SAP/WMS) and on-site warehouse operations. Technical Skills: * Advanced proficiency in SAP/WMS and MS Office (Excel pivot tables, macros). * Familiarity with warehouse automation tools (e.g., barcode scanners, RFID). * Bilingual (Chinese/English) is a plus - ability to interpret system manuals or communicate with global teams. Soft Skills: * Analytical mindset: Capable of translating operational issues into data solutions. * Detail-oriented: Ensures 100% alignment between system records and physical stock. * Adaptability: Thrives in a hybrid role bridging IT systems and frontline operations. * Hardworking and resilient under pressure #LI-EB1 #GS 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 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Scope: Job Scope: A leading biologics and CGT CDMO company in rapid expansion seeks a Senior Procurement Manager. The role focuses on designing strategies for optimal cost control, enhancing vendor management, achieving significant cost savings, and improving procurement sourcing and efficiency. Responsibilities include delivering insights to the executive team, standardizing business methodologies, evaluating procurement processes, and identifying improvement areas. Responsibilities: * Take full responsibility for the end-to-end procurement management of different categories, include but not limit to material, services, equipment, engineering and etc. * Align the Purchasing team's goals with organizational objectives, address complex issues by focusing on the needs of internal and external stakeholders to enhance sourcing and procurement processes, in line with global initiatives. * Develop, evaluate and maintain qualified supplier resources, and establish long-term partnerships with key suppliers, conduct regular supplier audit and performance evaluations. * Negotiate and manage purchasing contracts to improve key terms including price, payment terms, delivery lead time, quality standards and after-sales service, ensure quality and mitigate risks. * Coordinate and resolve the issues during the procurement process, including delivery delays, unqualified quality, return and replacement of the goods, to ensure the continuity of the company's production. * Responsible for implementation of purchasing control policy, development of working instructions and guidelines for users on how to deploy it, continuously drive process improvement. * Responsible for team building, staff training, develop KPIs and performance evaluations. * Manage the daily work of procurement team, formulate team work plans and objectives, guide subordinates in supplier development, price inquiry and comparison, contract signing and other work, and improve the overall professional procurement capabilities of the team. * Strictly comply with relevant pharmaceutical regulations (cGMP, FDA) and the company's internal procurement system to ensure the compliance of procurement processes and prevent procurement risk. Qualifications * Bachelor's degree or above in Business, Supply Chain Management, Engineering, or related field. * At least 10 years of procurement experience in biotech/pharmaceutical/CDMO, with expertise in cGMP procurement and regulatory compliance ((FDA/EMA, ICH Q7). * Proven ability to negotiate with vendors for favorable terms and cost reductions. * Proficiency in supply chain planning, forecasting demand, and managing inventory lead time to meet business needs. * Data-driven decision maker with exceptional leadership and communication skills, capable of setting clear visions and strategies. * Experience in leading multi-cultural teams, valuing diversity, and navigating global business dynamics. * Excellent technical skills, proficient in Excel, Word, PowerPoint, Project and SAP/S2P(Ariba or GEP) systems. * Expertise in strategic sourcing, evaluating and qualifying suppliers to optimize cost, quality, and supply reliability is preferred * CPSM(Certified Professional in Supply Management) or Six Sigma Green Belt is preferred The salary range for the role is 110k - 150k depending on experience and skill set 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 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Position Overview: We are seeking a Talent Acquisition Partner to join Genscript's team to conduct high-volume recruitment activities. Please note that this position is based onsite in Piscataway, NJ. The estimated salary range, dependent upon experience, is $60,000 - $70,000 base salary. Responsibilities: * Conduct high volume full-cycle recruitment activities to ensure successful Talent Acquisition from a technical and cultural perspective for open positions in US sites * Assist in the efforts of employer branding on social media and other channels * Develop recruiting channels to effectively perform searches for qualified candidates * Attend scientific conferences/tradeshows together with the sales & marketing team to advertise company positions * Manage campus recruiting, develop and maintain relationships with key contacts at target schools including academic faculty, career services, student organizations, etc. * Select qualified job applicants and make hiring recommendations when appropriate * Analyze employment-related data and prepare required reports * Conduct background and reference checks, along with e-Verify process * Conduct new employee orientation and interpret human resources policies, procedures, laws, standards, or regulations * Maintain current knowledge of Equal Employment Opportunity (EEO) and affirmative action guidelines and laws, such as the Americans with Disabilities Act (ADA) * Provide as needed support for continuous improvement projects, onboarding of employees and implementation of new HR services * Responsible for other duties as assigned Qualifications / Requirements: * Bachelor's degree in Human Resources Management * Experience in Human Resources in a fast paced environment * Headhunter or recruiting experience in life science industry is a plus * Excellent verbal and written communication skills * Strong interpersonal skills * Experience driving process standardization and improvement efforts * Proficiency in Microsoft Office applications, particularly Outlook, Word, Excel and PowerPoint #LI-EB1 #GS 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 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Scope: We are seeking a detail-oriented and capable Import and Export Shipping Specialist to efficiently handle the shipment of customer-provided materials, purchased materials, internal shipping requests, and import customs pre-entry activities. This position is based fully onsite in Piscataway, NJ and pays $26 per hour. Responsibilities: * Provide support in processing and verifying shipping documents for logistics operations. * Assist with communication with internal teams to ensure logistics processes align with production needs. * Inspect shipments for accuracy and report any discrepancies promptly. * Support packing and shipping processes as needed. * Assist with recordkeeping and data entry for daily order processing and shipping activities. * Assist with basic coordination with cold chain service providers and customs brokers. * Accurately enter data into the customs system based on shipping documentation. * Follow assigned Standard Operating Procedures (SOPs). * Perform other duties as required based on business needs. Requirements: Education: Minimum high school diploma, an associate's or higher degree in supply chain management or a relevant field is preferred Language: Fluent in both English and Mandarin is a plus. Physical Requirement: Ability to lift up to 50 lbs. Skills and Experience: * Strong organizational, communication, attention-to-detail, and problem-solving skills. * Strong time-management skills. * Ability to work effectively both independently and in a team environment. * Proficiency in MS Outlook, Excel, and Word. * Ability to communicate clearly, effectively, and professionally with personnel at all levels within the organization. * A can-do attitude and willingness to learn and meet customer and management expectations. #LI-EB1 #GS 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 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Title: Project Manager, Protein Expression Location: Piscataway, NJ (Fully Onsite) Job Summary: As a Project Manager - Molecular Biology, you'll lead customer-focused projects from strategy to delivery, ensuring high-impact outcomes in a fast-paced biotech environment. Leveraging your protein expression expertise, you'll oversee cross-functional teams, manage various accounts, and drive platform enhancements to maintain GenScript's competitive edge. The estimated salary range is $90,000 - $100,000, based on experience. Responsibilities: * Project evaluation: evaluate the project strategy and prepare the service proposal based on client`s request and scientific judgement. * Project management: Coordinate all teams to facilitate the research work, and provide regular feedback/update to client for any project progress/trouble shooting, especially for key accounts. * Work collaboratively with commercial team and production team to ensure projects can be finished in time. * Provide support to develop business from technical perspective. * Help to improve of service platform: Have a deep understanding of the market needs and our competitors. Help to optimize and upgrade our service package and platform technology. Qualifications: * At least MS degree in life sciences discipline with over 2-year protein science experience; PhD degree is preferred. * Strong customer service awareness, strong sense of responsibility, good communication and coordination ability, strong execution ability. * Solid protein related technical background, with understanding or hands-on experience. * Ability to multi-task and manage various project elements simultaneously. * Capacity to manage high stress situations. * Adaptive to bilingual working environment (English and Chinese). #LI-EB1 #GS 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 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Scope: The Lead Facility Engineer serves as the primary technical subject matter expert (SME) for mechanical, electrical, and plumbing (MEP) systems-particularly HVAC-during major facility construction and expansion projects (230,000+ sq ft plus additional lab buildouts). This role is responsible for ensuring that new facilities are designed, constructed, and commissioned to meet performance, safety, and compliance requirements. In addition to capital project responsibilities, the Lead Facility Engineer will provide high-level technical oversight of existing facilities, advising junior staff and aligning operational decisions with long-term reliability and efficiency goals. As GenScript grows its U.S. footprint, having robust, scalable infrastructure is essential. This role offers a rare opportunity to design foundational systems for how we manage equipment and facilities, while also driving in-house maintenance capability, energy efficiency, and cost optimization. Your leadership will directly influence operational resilience, response time, and long-term cost control. Details: This is a full-time role based onsite in Piscataway, NJ. The estimated salary range is $90,000 - $105,000, based on experience. Primary Responsibilities: * Serve as the HVAC/MEP technical lead for major capital projects, from design through commissioning. * Review and validate design documents, technical specifications, and contractor submittals for compliance with project requirements, codes, and best practices. * Coordinate with architects, engineers, and contractors to resolve design or field issues and ensure alignment with operational needs. * Oversee installation, testing, and commissioning of MEP systems, ensuring performance verification and turnover documentation are complete. * Support construction scheduling, cost control, and quality management, in collaboration with the Senior Construction Manager. * Lead and document punch list resolution for MEP scope. * Conduct periodic inspections and assessments of major building systems to identify risks or improvement opportunities. * Provide technical guidance to junior facilities staff and vendors managing day-to-day maintenance. * Lead the development and oversight of preventive maintenance plans for all facility-owned equipment (e.g., air handlers, boilers, pumps, compressors). * Set standards for CMMS (Computerized Maintenance Management System) usage and review work order trends, costs, and completion rates for improvement opportunities. * Oversee the planning and supervision of facility routines, preventive maintenance, and operational readiness across all sites. * Perform related strategic and technical work as assigned. Qualifications: * Bachelor's degree in Mechanical Engineering, Electrical Engineering, Civil/Structural Engineering, Architectural/Building Engineering, or a closely related field. * 4-6+ years of relevant experience in facilities/MEP engineering, construction, or capital projects within industrial, life sciences, or manufacturing environments. Includes experience in HVAC preventative maintenance, balancing, assessment, and knowledge of fabrication techniques. * 2+ years in a technical lead or supervisory capacity. * Proven experience as an HVAC/MEP SME on large capital projects (design review, field coordination, installation oversight, commissioning). * Experience with AutoCAD and MS Office. * Ability to read and interpret drawings, specs, and submittals, and coordinate RFIs/field changes. * Strong knowledge of the building process, construction principles, relevant codes, and industry standards. * Knowledge of controls and BMS (Building Management Systems). * Demonstrated ability to set up and oversee preventive maintenance strategies for mission-critical equipment. * Willingness to respond to urgent project or operational needs during and outside of normal working hours. Preferred * Experience in construction administration, commissioning, and startup of HVAC and mechanical/plumbing systems. * Experience in commissioning and system startup. * Understanding of EAV (Exhaust Air Valve), fume hoods, and ventilation requirements in specialized facilities. * Plumbing, HVAC and general contracting certifications are preferred. We're looking for Someone Who * Builds systems, not just reacts to problems - you design processes that prevent recurring issues. * Thinks like an owner - proactive, reliable, and focused on long-term outcomes. * Leads with clarity and empathy - your team knows where they're going and feels supported. * Communicates across levels - from technician to senior leadership, you know how to align. #LI-EB1 #GS 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.