Search the 26 jobs at GenScript

Provide full spectrum of administrative support for the Asia-Pacific Division of GenScript, including managing front-desk duties, ordering office supplies, assisting with travel arrangements, and optimizing operational processes.

The Sales Account Manager is responsible for driving sales efforts in a designated territory, implementing strategies for GenScript products and services. The role focuses on account management, building relationships, and achieving sales goals by understanding customer needs and aligning GenScript services with their research projects.

The Senior QC Specialist is responsible for coordinating quality control and assurance tasks, troubleshooting key orders, statistics and analysis of production data, managing promotion projects, formulating standard operating procedures, monitoring quality and safety inspections, and training junior employees.

The HR Specialist will support HR functions like employee relations and benefits administration, mediate conflicts, conduct employee interviews, and spearhead recruitment efforts. The role involves managing HR operations while ensuring compliance with policies and laws, and assisting with onboarding/offboarding processes as well as diversity initiatives.

The Embedded System Engineer will design and develop embedded software and firmware for semiconductor array-based DNA synthesis platforms, focusing on digital circuit design and ARM microcontroller programming. Key responsibilities include hardware communication integration, firmware development for fluidic monitoring systems, and PCB design.

The Scientist in Quality Systems enhances ProBio’s quality systems by ensuring compliance with GMP regulations for clinical and commercial Cell and Gene Therapy products. Responsibilities include quality assurance reviews, supporting investigations and CAPA processes, and collaborating with internal teams to improve GxP compliance.

The Sr. Product Manager will be the key product owner for gene and cell therapy services, performing launch planning, market trend analysis, and product development roadmapping. They will lead business initiatives, collaborate with stakeholders, and advocate for customer needs.

The GMP Logistics Specialist is responsible for overseeing domestic and international logistics processes including shipment coordination, customs clearance, and maintaining compliance with GMP standards. The role involves collaboration with cross-functional teams, handling shipping records, and managing freight invoices while adhering to cGMP policies.

The Office Admin Coordinator will oversee office administration tasks, manage staff, coordinate company events, handle travel arrangements, and budget oversight. The role requires proactive management to ensure efficient operations, support various departments, and implement cost-saving initiatives.

The Legal Assistant will support the legal team at GenScript by ensuring compliance with corporate obligations of foreign subsidiaries, preparing and maintaining corporate compliance documentation, drafting legal documents, and assisting in the formation of new legal entities.

Senior Logistics Specialist responsible for shipping document confirmation, shipping execution, forwarder and broker management, and inbound/outbound shipment tracking. Ensures on-time delivery, compliance with customs regulations, and cost-effective logistics operations for a global biotechnology group and its subsidiary.

The QC Associate Scientist will perform a variety of analytical tests to support QC processes for clinical trial materials. Responsibilities include ensuring compliance with cGMP requirements, conducting method development and validation, and optimizing QC department initiatives. The role requires strong technical knowledge and the ability to support quality control testing for various biological products.

The QA Technical Operations Specialist is responsible for managing supplier quality activities, overseeing the GMP supplier qualification program, conducting quality assessments, managing vendor complaints, and ensuring compliance with quality standards. The role involves data analysis for supplier performance, driving improvements, managing audits, and supporting validation and regulatory inspections.

The Office Admin Supervisor is responsible for overseeing office operations, managing administrative services, coordinating travel arrangements, supporting external personnel, leading events, managing office supplies, supervising billing and data management, and providing operational support across departments.

The Bioprocess Specialist in Downstream Processing performs key tasks including preparation of solutions, chromatography, filtration, and drug formulation. This role requires adherence to regulatory standards and collaboration with departments on gene therapy manufacturing.

The Sr. Automation Engineer is responsible for managing the SCADA system and automation systems in GMP manufacturing. Responsibilities include installation, maintenance, validation of systems, and adherence to regulatory requirements. The role involves collaboration with internal departments and supports automation for bioprocess equipment and change management processes.

The Senior Regional Marketing Specialist at ProBio will lead initiatives in content development, campaign management, and lead generation to enhance client acquisition. Responsibilities include collaborating with sales teams, managing nurturing campaigns, overseeing industry events, and optimizing marketing strategies based on performance data.

GenScript ProBio seeks a Corporate Legal Counsel to lead the development and implementation of global legal and regulatory strategies, provide legal advice on various topics, manage external legal counsel, and stay updated on legal developments impacting the business.

The Bioprocess Specialist in Upstream Processing will prepare stock solutions and media, operate bioreactors, and support manufacturing processes while adhering to regulatory requirements and cGMP. Responsibilities include monitoring cell cultures and fermentation processes, maintaining clean room standards, and authoring preparation records.

The QA Specialist will oversee quality management systems, perform release of materials and products, and ensure on-site quality monitoring. They will analyze quality data, investigate product complaints, and provide quality-related training, working closely with production and support departments.