Automation Specialist

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.

Key Responsibilities:

- Develop and qualify automated methods for Cell therapy QC assays . 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 . Hamilton and lab orchestration software . 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

Required Qualifications:

- Bachelors in Life Sciences Engineering or related field with 5 years in analytical bioanalytical or automation assay development. Masters with 3-5 years in the same area. . 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 . 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.

Preferred Qualifications:

- Experience with programming languages Python Visual Basic etc. for automation workflows.

- Experience in aseptic technique and bioprocess sample handling.

- Experience in analytical method development for cell therapy or biologics.

This is a Contract position based out of Seattle, WA.

The pay range for this position is $56.45 - $71.69/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Seattle,WA.

This position is anticipated to close on Mar 3, 2026.