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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 (CGT), 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. In terms of plasmid service, ProBio supports the most clinical approvals for CGT drugs including mRNA vaccines, CAR-T in China. It is also the first GMP manufacturing platform to provide in vitro transcription (IVT) template linearized plasmids for mRNA vaccines and has supported several mRNA vaccine global enterprises to obtain clinical approvals. In terms of viral vector service, ProBio has a stable and high-yield viral vector platform.

Job Scope:

As the Plasmid Production Assistant Researcher, you will follow the guidance of the job-specific Standard Operating Procedure (SOP). A series of experimental procedures will be conducted, including cell lysis, column purification, and plasmid recovery, to extract the target genes required by customers.

Location: Piscataway, NJ

Responsibilities:

• Responsible for the daily maintenance, repair, inspection, and other work related to the department's basic equipment, as well as the writing of experimental records and 5S management.
• Operate according to SOP (Standard Operating Procedures), complete daily production operations, including material preparation, equipment cleaning and maintenance, etc., and provide feedback on any abnormalities in upstream and downstream positions.
• Master the online MES (Manufacturing Execution System) process synchronization operations to ensure data traceability.
• Customize reagents according to production throughput, in compliance with 5S on-site management requirements, such as reagent expiration dates and reagent positioning labels.
• Propose specific production process optimization suggestions, and undertake the specific production work of department process optimization and technical improvement.
• Assist with the completion of related tasks within the department and external positions, and complete temporary tasks assigned by superiors.

Qualifications:

• Educational Background: Possess a bachelor's degree in Biology, or a related field, demonstrating a strong foundation in the sciences.
• Proficient in the professional theoretical knowledge of the position, and able to report problems in time.
• Master the professional theoretical knowledge related to the position and understand the upstream and downstream related processes.
• Master the working principle of the equipment, and be responsible for the maintenance and upkeep of the team equipment.
• Strong interpersonal communication, coordination and organization skills.
• Strong ability to analyze and deal with problems, clear thinking and careful consideration of problems.
• Meticulous, serious, responsible and patient.