Automation Engineer

Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.

The position reports to the Director of US Molecular Biology R&D at the Piscataway site of the GenScript Gene R&D department.

1. →Develop new automation workflows to meet the high throughput biomanufacturing needs.
2. →Maintain and upgrade existing automation methods.
3. →Provide hands-on support, troubleshooting, and maintenance for individual lab instruments and larger integrated automation systems.
4. →Diagnose and resolve complex mechanical, software, and system integration issues to minimize equipment downtime and maintain operational continuity.
5. →Manage project timeline and leverage internal resources to push project forward.
6. →Closely communicate with other teams to ensure the smooth tech transfer.

1. Bachelor’s degree in mechanical engineering, biomedical engineering, and other related fields.
2. 1+ year of relevant experience of automation development in biomanufacturing environment.
3. Experience with laboratory instrumentation and automation systems.
4. Excellent communication and organization skills.
5. Experience troubleshooting liquid handling instruments such as Tecan Fluent, Hamilton STAR.
6. Extensive experience in writing scripts/protocols for Tecan, Hamilton, Thermo Momentum Scheduler.
7. Experience with molecular biology experiments is a plus not a must.

• Basic understanding of equipment communication, networking, TCP/IP, serial communication, or automation software is a plus.
• Basic programming or scripting experience is a plus.
• Experience in a biotechnology, pharmaceutical, laboratory, or regulated manufacturing environment is a plus.