Senior Technical Specialist

caprion; Lake Forest (CA); On-site; USD 97,000 - 120,000; Full time

Benefits offered by this job

Competitive wages

Medical, dental, and vision benefits

401(k) retirement savings plan with a

Vacation and sick time

Employee Assistance Program (EAP)

Referral Program

Job summary

CellCarta seeks a Senior Technical Specialist to support assay operations, training, troubleshooting, and laboratory excellence in a fast-paced CLIA environment. You will collaborate with internal teams to ensure quality and compliance while contributing to innovative research.

You will coordinate assay runs, validate histochemistry and in situ techniques, assist with equipment maintenance, and support audits and project execution.

Qualifications

• CLIA personnel requirements to perform moderate- or high-complexity testing.
• Experience with Ventana Benchmark, Leica Bond Rx, Dako Autostainer Link 48; Omnis a plus.
• Knowledge of GCP, GCLP, and GLP.
• Strong communication skills and English proficiency.
• Ability to interpret protocols and safety rules in English.

Responsibilities

• Coordinate assay runs and monitor project status.
• Support optimization and validation of histochemistry, immunohistochemistry, in situ hybridization, and related assays.
• Assist in technical training and maintain training documentation.
• Assist with troubleshooting and preventive maintenance of laboratory equipment.
• Act as SME for client calls or audits as needed.
• Maintain tissue bank inventory and procurement.
• Prepare reagents and perform staining and in situ hybridization per SOPs.

Skills

Good communication skills

Problem-solving

English proficiency

Education

Bachelor's or Associate degree in medical/clinical laboratory science or related field

Tools

Ventana Benchmark

Leica Bond Rx

Dako Autostainer Link 48

Dako Omnis

Job description

Senior Technical Specialist

Ready for your next career opportunity? CellCarta, a Contract Research Organization, is looking for a Senior Technical Specialist to join our team. In this role, you will contribute to assay operations, technical training, troubleshooting, and laboratory excellence while supporting innovative research that advances human health. Join a collaborative team of talented professionals and make an impact through your work.

Summary

The Senior Technical Specialist supports assay operations, laboratory processes, technical training, and equipment maintenance to ensure high-quality and compliant laboratory activities. This role serves as a technical resource for internal teams, assists with assay troubleshooting and validation, and supports project execution, audits, and continuous process improvement.

Responsibilities

• Assist with coordinating and scheduling assay runs, and monitor the completion status of assigned projects
• Support activities for optimization and validation of histochemistry, immunohistochemistry, in situ hybridization, immunofluorescence, and other laboratory-developed assays
• Assist in technical training, staff education, and competency assessments. Develop and maintain training documentation, bench training forms, training guides, and troubleshooting reference materials, and ensure appropriate training of laboratory staff through instruction and hands-on demonstrations
• Assist with troubleshooting, validation, qualification, and preventive maintenance of laboratory equipment. Communicate with vendors as needed and ensure maintenance documentation is completed in a timely manner
• Assist with client calls and/or audits as a SME, as needed/applicable, and serve as an internal technical resource for project managers and other internal teams
• Assist in maintenance and inventory of the tissue bank and tissue sample procurement
• Initiate and QC new specification worksheets and autostainer protocols
• Assist with tracking and managing all staining protocols and versions
• Coordinate and assist with assay transfer across CellCarta laboratories
• Provide feedback to management regarding challenges relating to laboratory operations and assay development
• Monitor the schedule for and completion of equipment preventive maintenance and other recurring events required for regulatory compliance
• Prepare and QC reagents and solutions according to SOPs or approved written instructions
• Perform histochemical and immunohistochemical staining according toSOPs and protocols
• Perform in situ hybridization according toSOPs and protocols
• Perform clinical, non-clinical, and internal research projects approved by management or the Medical Director
• Maintain detailed and accurate records of all assays and results
• Perform other duties as assigned by management

Education

• Bachelor's degree in medical technology, clinical laboratory science, chemical, physical, or biological science; or an Associate degree in chemical, physical, or biological science, medical laboratory science, or an equivalent combination of education and training is preferred

Main Requirements

• Candidates must meet CLIA personnel requirements to perform moderate- or high-complexity clinical sample testing or inclusion criteria testing for clinical trials
• Experience with the Ventana Benchmark, Leica Bond Rx, and Dako Autostainer Link 48 platforms is preferred. Experience with the Dako Omnis platform is a plus
• Knowledge of GCP, GCLP, and GLP
• Good communication skills
• Ability to read and interpret documents such as protocols, safety rules, and procedure manuals written in English, and to record results in English
• Ability to solve practical problems and interpret a variety of instructions provided in written, oral, or schedule form

Working Conditions

• Monday to Friday, 5:30 a.m.to 1:30 p.m.(40 hours per week)
• 100% onsite

Benefits

• Competitive wages ($96,600 - $120,000 USD)
• Medical, dental, and vision benefits
• 401(k) retirement savings plan with a healthy match
• Vacation and sick time
• Employee Assistance Program (EAP)
• Referral Program

About CellCarta

CellCartais a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China.

Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!

The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.

CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact [e-mail].