Search the 21 jobs at GenScript

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.

The Project Manager will oversee customer projects, ensuring deliverables meet the established scope. Responsibilities include project evaluation and strategy development, coordinate internal teams for research, communicate updates to clients, and improve service platforms based on market needs.

The IT Project Manager will lead project management for specified initiatives, coordinate contributions from stakeholders, ensure services are delivered within agreed timelines, manage project plans, engage internal stakeholders, report on progress, identify revenue opportunities, and support team objectives.

The Technical Account Manager is responsible for managing customer service operations, providing technical advice, collaborating with Sales Account Managers, handling inquiries, and ensuring customer satisfaction through effective communication and problem-solving techniques.

Sales Account Manager responsible for implementing sales and marketing strategies to achieve sales and profit goals in Tokyo, Japan. Must achieve sales targets, develop sales strategies, and collaborate with internal teams and key customers. Requires a Masters or PhD in Biology/Life Science and 1 year of lab experience.

The Campaign Manager will lead and execute marketing campaigns to promote products and services at GenScript. Responsibilities include strategy development, execution management, collaboration with cross-functional teams, market research, performance monitoring, and ensuring regulatory compliance.