
Automation Specialist
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Overview
Job Description
- 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, HighRes BioSolutions).
- 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.
The hourly rate for this position is between $70.00-$72.00 per hour.Compensation: Factors which may affect starting pay within this range may include [geography/market, skills, education, experience and other qualifications of the successful candidate].
Benefits: Sunrise offers ACA compliant medical coverage/dental insurance/vision insurance to all employees. We also offer Sick time benefits as required per State regulations.Contact: Sunny Rajput | sunny.r@sunrisesys.com | URL:
Automate your job search with Sonara.
Submit 10x as many applications with less effort than one manual application.
