Search the 25 jobs at GenScript

The QC Associate Scientist is responsible for conducting analytical tests such as UV-Spectrophotometry and HPLC, supporting QC-Analytics initiatives, ensuring compliance with cGMP and regulatory requirements, and optimizing QC department initiatives. This role aids in the technology transfer process and contributes towards the delivery of clinical trial materials.

The QA Technical Operations Specialist will oversee quality assurance standards, manage supplier quality activities, and support strategic supplier management to enhance quality and reduce costs. Responsibilities include overseeing material release processes, conducting supplier audits, ensuring compliance with GMP and quality procedures, and driving root cause analysis for non-conformance issues.

The Bioprocess Specialist will execute downstream processing tasks including preparation of solutions, filtration, chromatography, and drug formulation. The role requires adherence to regulatory compliance and collaboration with internal and external stakeholders.

The HR Generalist position will collaborate with leaders to provide HR insights, support talent acquisition, employee relations, and drive HR initiatives for organizational effectiveness at GenScript in Piscataway, NJ. Responsibilities include workforce planning, supporting performance reviews, change management, and maintaining compliance and HR data management.

The Sales Account Manager is responsible for implementing sales and marketing strategies for biotech products/services in North Italy and Ticino, Switzerland. This includes developing sales strategies, working with cross-functional teams, managing customer relationships, and utilizing CRM for pipeline management.

The Senior Project Manager will oversee complex projects in the biotech sector, managing project planning, execution, stakeholder communication, area of quality assurance, and risk management to ensure quality products are delivered on time and within budget.

The Sr. Automation Engineer will manage and maintain automation systems on GMP manufacturing equipment, including SCADA and BAS. Responsibilities include performing validation, system administration, and project management. The role requires cross-functional collaboration and adherence to regulatory requirements in the biotech industry.

The Regional Marketing Specialist will drive lead generation and marketing initiatives for ProBio by developing content, executing omni-channel campaigns, managing events, and collaborating with sales teams to achieve marketing goals. This role involves continuous analysis and optimization of marketing strategies to enhance brand awareness and customer engagement.

The Legal Counsel at GenScript ProBio is responsible for providing legal advice, managing global legal and regulatory strategies, overseeing outside counsel, and ensuring compliance with legal regulations within the biotechnology and pharmaceutical sectors.

The Bioprocess Specialist will execute upstream processing activities by preparing solutions, operating fermenters and bioreactors, and conducting cell culture. They will adhere to GMP and standard procedures, monitor processes, and assist in documentation and quality checks within a cleanroom environment while collaborating with teams to ensure efficient operations.

The Bilingual Project Manager will manage customer projects, ensure deliverables are met, and communicate progress to clients. Responsibilities include project evaluation, coordination with teams, market understanding, and daily operations support.

The Technical Account Manager is responsible for overseeing daily customer service operations, addressing inquiries, providing technical advice, collaborating with Sales Account Managers to enhance customer satisfaction, and delivering technical presentations to clients.

The Sales Account Manager is tasked with implementing sales strategies to achieve profit goals in their territory. Responsibilities include reporting on sales activities, collaborating with teams, expanding market reach, and driving business initiatives in the life sciences sector.

The HR Coordinator will support onboarding, manage employee documentation, serve as a point of contact for inquiries, process HR invoices, assist with employee benefits administration, document processes, coordinate training and engagement events, and handle other tasks as assigned.

The EHS Specialist will develop, implement, and monitor EHS programs to ensure compliance with regulations, assess safety conditions, lead training sessions, oversee waste management, and enforce safety goals to promote a safe work environment.

The Sales Account Manager is responsible for driving sales efforts and implementing marketing strategies for GenScript products and services within the assigned Boston territory. Key tasks include developing territory sales strategies, understanding customer needs, building relationships, and achieving sales targets.

The Senior QC Specialist coordinates QC and QA work, manages production data, participates in various promotion projects, formulates SOPs, trains junior staff, monitors quality and safety inspections, and completes tasks as assigned by the supervisor.

The Embedded System Engineer will develop, optimize, and deploy embedded software and circuit designs for a DNA synthesis platform, focusing on firmware development and hardware integration. Responsibilities include designing digital circuits, programming ARM microcontrollers, and supporting communication with synthesis hardware.

The Sales Account Manager will drive sales efforts in the assigned territory for GenScript products. Responsibilities include developing sales strategies, managing accounts, conducting customer visits, and collaborating with teams to achieve sales goals. The role requires a scientific background and understanding of customer needs in life sciences.

The Scientist, Quality System will enhance ProBio’s quality systems by supporting GMP quality management for Cell and Gene Therapy products. Responsibilities include quality support for change controls, deviations, investigations, and CAPAs, ensuring compliance with regulatory requirements and internal SOPs.