Laboratory Automation Engineer II

Labcorp • San Francisco, CA

17h • $95,000 - $130,000

About The Position

Imagine being involved with innovation that changes the course of our industry daily! At Labcorp, we advance science, technology and innovation and recognized as one of the most respected companies in the world. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. We have an excellent career opportunity for a Laboratory Automation Engineer II to join our dynamic team in San Francisco, CA! (This position does not offer employment visa sponsorship.) Position Summary The mid-level Laboratory Automation Engineer will independently program and develop methods for liquid handlers, contributing to the design of efficient laboratory processes. They will be responsible for installing, integrating, and maintaining laboratory automation hardware and software , including programming third-party automation systems. This role includes collaborating with cross-functional teams, conducting experiments, and performing system validations. They will also provide process documentation, conduct training, and support troubleshooting efforts.

Requirements

• Bachelor's degree in Engineering, Life Sciences or related field
• 4 or more years of experience in a laboratory automation role; equipment and clinical laboratory roles relevant
• Experience in a high throughput CAP/CLIA, ISO 13485/15189 , GMP regulated environment
• Proficient in industry standard laboratory automation platforms (liquid handlers, work cells, scheduling software, etc.) and other commonly used laboratory equipment
• Experience with participation in or running with FMEA & RCA
• Ability to work independently and with minimal supervision

Nice To Haves

• Technical proficiency and proven success in laboratory automation and systems development and integration for the life science industry; especially with robotics and liquid handling systems
• Flexibility and self-initiative required to support several simultaneous automation projects
• Strong experience engaging cross-functionally in a high-collaboration environment
• Experience with equipment functionality and validation testing
• Strong organizational skills, as well as written and verbal communication skills
• Software development experience in one or more languages (C#, Python, etc.)
• Experience working under regulatory regimes such as CLIA, CAP, or FDA

Responsibilities

• Utilize data-driven insights to improve existing automation platforms, ensuring efficiency, reliability, and scalability.
• Own individual projects to enhance automation workflows, incorporating best practices in lab automation, data analysis, and process optimization.
• Partner with Production Support Engineering and Production Lab teams to implement lab automation enhancements and resolve escalated issues.
• Independently operate, troubleshoot, and optimize a wide range of lab instruments and automated platforms (liquid handlers, work cells, scheduling software, etc.).
• Perform calibration and validation to ensure instrument reliability when applicable.
• Write protocols and methods to automate laboratory processes, control instruments, and manage data.
• Contribute to software integration and testing methodologies.
• Design and implement solutions to connect laboratory instruments, devices, and software platforms using standard communication protocols.
• Develop validation protocols for automated workflows, perform risk assessments, and ensure quality control measures align with regulatory requirements.
• Assist in transitioning new automation platforms from development to production by defining stability metrics and validating performance.
• Regularly review instrument data to identify trends, mitigate risks, and propose long-term solutions.
• Take ownership of individual project execution, manage tasks & timelines, and provide guidance to junior team members to elevate team capabilities.
• Participate and lead in FMEA and RCA as needed.

Benefits

• Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.
• Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only.
• Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level