Automation Engineer I, R&D

AbbottMadison, WI
Onsite

About The Position

The Automation Engineer I will join a highly collaborative, cross-functional team including Systems Development, R&D, Operations and IT to develop and deploy robust laboratory automation solutions for pre-analytical sample processing, Immunoassay , and Next-Generation Sequencing based assays in support of high complexity medical devices. This role requires experience working on a collaborative, fast-paced team to build scalable, highly integrated automation platforms which enable users to reliably and efficiently deliver timely, high-quality results that directly impact patients’ lives in a n FDA regulated environment. This role requires employing engineering concepts across many disciplines (software, mechanical, electrical, biomedical, etc.) to solve problems within complex systems.

Requirements

  • B.S. in Life Sciences, Engineering, or field as outlined in the essential duties.
  • 1+ years of experience working with automated liquid handlers and associated software in a regulated environment (CLIA, CAP, ISO, etc.).
  • High attention to detail and proven ability to effectively communicate across teams located at multiple sites.
  • Optimistic and innovative; solution oriented.
  • Proven ability to troubleshoot technical issues in collaboration with a team of scientists.
  • Experience working in a fast-paced environment with changing priorities and demands.
  • Values, communicates, and interacts with others with high levels of transparency and respect.
  • Familiarity with Next-Generation sequencing and/or common molecular biology laboratory workflows.
  • Proficient in Microsoft Office programs, such as: Word, Excel, PowerPoint, Outlook, Access, OneNote, and Publisher.
  • Demonstrated ability to perform the essential duties of the position with or without accommodation.

Nice To Haves

  • Experience with Hamilton liquid handlers is desired.
  • M.S. degree in Life Sciences, Engineering, or field as outlined in the essential duties.
  • 2+ years of experience working with automated liquid handlers and associated software in a regulated environment (FDA, CLIA, CAP, ISO, etc.).
  • Experience with Hamilton liquid handlers is desired.
  • Knowledge of the software development lifecycle for a medical device.
  • Strong technical writing skills.
  • New grads welcome to apply.

Responsibilities

  • Develop automated laboratory solutions through programming of liquid handling robotics platforms to meet the requirements of existing assay workflows , in an FDA regulated medical device environment .
  • Participate in all aspects of the software development lifecycle.
  • Work with cross-functional teams to understand laboratory processes and procedures and translate into user needs and software requirements.
  • Develop robust automated liquid handler methods for scalable and high throughput use that integrate with larger software systems for data management and sample tracking.
  • Iteratively develop and improve software based on feedback from experimental data and user feedback.
  • Maintain and improve the performance of existing software.
  • Troubleshoot issues across electrical, mechanical, and software systems to perform root cause analysis and issue resolution.
  • Review and debug complex software.
  • Design experiments studying impact of software controls on mechanical systems.
  • Use good documentation practices to write test protocols, execute experiments according to protocols, write test reports, and manage deviations.
  • Write technical documents under formal design controls for medical devices with team input, including but not limited to software requirements and software design descriptions.
  • Ability to establish high level of credibility and maintain effective relationships and strong open communication with employee, managers, and customers.
  • Ability to meet critical deadlines and successfully facilitate constructive engagements.
  • Ability to integrate and apply feedback in a professional manner.
  • Ability to prioritize and drive to results with a high emphasis on quality.
  • Ability to work with moderate supervision and take ownership of assigned projects.
  • Ability to follow and optimize processes.
  • Ability to work as part of a team.
  • Strong interpersonal skills, detail oriented, with strong organization and time management skills.
  • Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
  • Support and comply with the company’s Quality Management System policies and procedures.
  • Maintain regular and reliable attendance.
  • Ability to act with an inclusion mindset and model these behaviors for the organization.
  • Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.
  • Ability to travel 5% of working time away from work location, may include overnight/weekend travel.

Benefits

  • An excellent retirement savings plan with a high employer contribution.
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