Automation Specialist

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 ResponsibilitiesDevelop, 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-offRequired QualificationsBachelor?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 areas3-5 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.Preferred QualificationsExperience 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.100% onsiteWork Schedule: Mon-Fri (normal business hours)This posting is for a contract assignment with ASK Staffing DBA ASK Consulting to provide services to Bristol Myer-Squibb.The starting hourly compensation for this assignment is the following range ($56- $59.75/hr). While the final, individual compensation and any available benefits will be determined by your employer of record ASK Staffing, Inc (and not BMS), factors that will be included in making the final determination may include the characteristics of the assignment, such as demonstrated experience, required skill, and the geographic location where the job is performed. The starting hourly compensation may be subject to change.About ASK ConsultingASK Consulting is an award-winning, woman-owned staffing and recruitment solutions provider with over three decades of industry experience. We specialize in connecting businesses of all sizes?across IT, healthcare, engineering, finance, and more?with top-tier professionals. Backed by a global network and personalized service approach, our team is dedicated to building meaningful partnerships that drive organizational success and empower job seekers to excel in their careers.BenefitsASK Consulting provides comprehensive, ACA-compliant health coverage, along with dental, vision, Short- and Long-Term disability for eligible employees. We also offer commuter benefits, a 401(k) plan with no matching, and a referral bonus program. In addition, ASK Consulting offers unpaid leave and paid sick leave as required by law.Equal Opportunity EmployerASK Consulting is an equal opportunity employer and does not discriminate against employees or applicants based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other classification protected by federal, state, or local laws.California Applicant NoticeASK Consulting is committed to complying with the California Privacy Rights Act (?CPRA?), effective January 1, 2023, as well as all relevant data privacy laws in the jurisdictions where we recruit and hire. To learn more, please review our Notice to California Job Applicants Regarding the Collection of Personal Information on our website. 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Findings that raise concerns may result in withdrawal of a conditional job offer.To learn more about how ASK Consulting collects and uses personal information during the recruiting process, please review our Privacy Notice andCCPA Addendum. As part of our recruitment efforts, we may ask you to disclose various categories of personal information, including identifiers, professional details, commercial information, educational background, and other related data. ASK Consulting will use this information solely to facilitate the recruitment process.This posting does not constitute an offer of employment. All applicants seeking positions in the United States must be legally authorized to work in the United States. Submitting intentionally false or fraudulent information in response to this posting may disqualify you from consideration. Any eventual offer of employment will be considered ?at will,? regardless of the expected assignment duration.