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Engineering - Automation Specialist

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Spectraforce Technologies

Warren, NJ (In Person)

Full-Time

Posted 2 days ago (Updated 4 hours ago) • Actively hiring

Expires 6/8/2026

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Job Description

Engineering - Automation Specialist Spectraforce Technologies United States, Jersey, Warren May 08, 2026
Position Title:
Engineering -
Automation Specialist Work Location:
Devens, MA Assignment Duration:
12
Months Work Schedule:
Mon-Fri(normal business hours)
Work Arrangement:
100% onsite
Must Haves:
  • 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).
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 (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
Qualification & Experience:
  • 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.
Working Conditions & Physical Demands (If Applicable): Lab w/o blood & animal Position Handles Hazardous Materials

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