Automation Specialist

Work Schedule:
Mon-Fri(normal business hours)

Position Summary:

We are seeking an experienced contractor to support the development, qualification, and implementation of automated QC methods for cell therapy assays. This hands‑on role will focus on designing, programming, and optimizing automation scripts and workflows for platforms such as Hamilton and Tecan, ensuring seamless technical transfer and compliance within a GMP environment. The successful candidate will collaborate with QC, analytical development, and automation teams to drive continuous improvement and operational excellence in automated QC systems.

• Develop, and qualify automated methods for Cell therapy QC assays (e.g., flow cytometry, cell‑based assays, molecular‑based assays, and cell viability) using automated liquid handlers and integrated platforms.
• Program and troubleshoot scripts for liquid handlers (e.g., Hamilton) and lab orchestration software (e.g. Cellario).
• Demonstrate that automated assay scripts developed from manual methods are comparable, robust, and fit for intended use through execution of defined development studies.
• Author development reports, work instructions, and supporting technical documentation in compliance with GMP requirements, and support associated validation activities as required.
• Drive troubleshooting and continuous improvement initiatives for automated workflows and systems.
• Drive training sessions and supporting documentation to support hand‑off.

• Bachelor’s in Life Sciences, Engineering, or related field with 5+ years in analytical, bioanalytical, or automation assay development. Master’s with 3–5 years in the same area. Ph.D. with 1–3 years in the same areas.
• 3-5 years of hands‑on experience in automation of biologic and Cell Therapy assays.
• Demonstrated proficiency in developing and programming automation scripts for liquid handlers (Hamilton, Tecan, or similar platforms).
• Experience with integrated automation systems and lab orchestration tools (e.g., Cellario, High Res Bio Solutions).
• Strong problem‑solving skills and ability to troubleshoot automated workflows and hardware/software issues.
• Familiarity with regulatory requirements for QC in the biopharmaceutical industry and experience supporting audits and inspections.
• Excellent communication and interpersonal skills, with the ability to work collaboratively across multidisciplinary teams.
• Flexibility and eagerness to learn new technologies and techniques.

• Experience with programming languages (Python, Visual Basic, etc.) for automation workflows.
• Background in aseptic technique and bioprocess sample handling.
• Experience in analytical method development for cell therapy or biologics.