At Adaptive, we’re Powering the Age of Immune Medicine. Our goal is to harness the power of the adaptive immune system to transform the way diseases are diagnosed and treated.
As an Adapter, you’ll have the opportunity to make a difference in people’s lives. With Adaptive, you’ll create a career highlight through collaboration with bright, curious colleagues working at the apex of innovation and application.
It’s time for your next chapter. Discover your story with Adaptive.
Position Overview
The Clinical Lab Technologist position willbe responsible forprocessing medically relevant biological samples through extraction and/or high throughput next-generation DNA sequencing assays. This role will work within a team of Laboratorians in a fast-paced, high production setting to process research and clinical diagnostic samples to provide test results to patients, oncologists and other medical practitioners and researchers. As such, high attention to detail and clinical mindedness are crucial to success in this role.
Adaptive’sclinical laboratories are CLIA/CAP/NYS/FDA certified, and as such this position needs to adhere to and uphold all applicable regulatory requirements.
Possible working shifts include:
- AM shift: Friday - Tuesday 6:00am - 2:30pm
- PM shift: Friday - Monday 12:30pm - 11:00pm
Position levelI,II, or IIIisdeterminedby candidates’education, experience, and competencies as defined below:
Scope/Impact
Level I
- Performs and providesgeneral supportfor DNA extractions, PCR amplification, or high-throughput sequencing assays on DNA librariesin accordance withstandard laboratory processes and procedures.
- Operates andmaintainslaboratory equipment such as liquid handling robotics and DNA sequencers.
- Completestasks asassigned (e.g.routine clinical or research sample processing, validations, reagent QC runs, or special projects) accurately while following strict methodologies.
- Provides guidance toless-experiencedstaff.
Level II
As well as:
- Performs training and/or competency assessments for Clinical Laboratory Technician/Technologist team members on high complexity molecular methods.
Level III
As well as:
- Suggestschanges to existing laboratory procedures and processes to improve efficiency and results.
Complexity
Level I
- Performs protocols under compliance with regulatory agencies,modelsappropriate clinical, regulatory and safety practices.
- Makes decisions thatimpactquality, timeliness, and effectiveness of the team.
- Resolves basic problems that may involve uncommon variations of issues.
- Identifiesand uses upto date,accurateinformation for problem solving and analysis.
- Ensurescompliance with lab regulatory agencies (GxP, FDA, ISO).
- Keepsaccurateand detailed records for all workflows following Good Documentation Practices.
Level II
As well as:
- Suggests improvements to existing laboratory procedures and processes to improve the efficiency of the team.
- Works on assignments requiring considerable clinical judgement and initiative.
- Understands implications of their work performance and when to elevate issues upward.
Level III
As well as:
- Identifiesand uses knowledge of how supporting teams function withownteam.
Knowledge/Level of Expertise
Level I
- Demonstrates excellent clinical judgment and integrity bypossessingspecialized skills through job-related training and considerable on-the-job experience.
- Explainstechnical information within the team.
- Demonstrates understanding of underlying scientific principles of analytical methods and provides relevant information to Supervisor or Lead Technologist toassistwith troubleshooting assay or instrument issues leading toappropriate correctiveactions.
- Has strong communication skills to present problems or issues to Supervisor or Lead Technologist.
- Handlessensitive information confidentially.
Level II
All oftheabovewith considerable knowledge/skills in a range of laboratory procedures.
Level III
All ofthe abovewith deep knowledge/skills in a range of laboratory procedures.
Interactions, Supervision and Discretion
Level I
- Exhibit clear and effective communication tofacilitateeffective handoff procedures.
- Followsstandardized laboratory processes and procedures with some guidance on daily work.
- Usesclinical discretion to make recommendations for improving work procedures and processes to improve efficiency.
Level II
As well as:
- Provides guidance to more junior team members.
Level III
As well as:
- All ofthe above with independence, andfrequentlyapplieseducated discretionin decision making.
Regulatory Responsibility
Level I,II, andIII:
- Maintain continuing education credit requirements.
- Record nonconformances for allappropriate errors.
- Enter and track data in a laboratory information database (LIMS)
- Operate andmaintainlaboratory equipment such as liquid handling robotics and DNA sequencers.
- Regulatory responsibilities per Good Manufacturing Practices (GMP)
- Regulatory responsibilities per Good Clinical Practices (GCP)
- Regulatory responsibilities per Good Laboratory Practices (GLP)
- Regulatory responsibilities of “Testing Personnel” for high complexity testing as defined by 42CFR493.1495
- All other duties as assigned
Position Requirements (Education, Experience, Other)
Required
- Molecular biology skills (e.g.DNA Extraction, Purification, PCR, qPCR, next-generation DNA sequencing) and related technical knowledge.
- Experience working with human specimens (e.g.blood,tissuesand/or cells) and biohazardous material.
- Strong communicationand interpersonal skills,abilityto collaborate across teams and disciplines.
As well as:
Level I
Must meet ONE of the following:
- Bachelor’s or higher in medical technology or laboratory science from an accredited institution, OR:
- Bachelor’s or higher in one of the chemical or biological sciences from an accredited institution + 6 months of high-complexity molecular experience and/or training in a clinical laboratory(holding a CLIA Certificate of Compliance/Accreditation)
Level II
Must meet ALL of the following:
- Bachelor’s or higher in medical technology or laboratory science, chemical science, or biological science from an accredited institution.
- Minimum of 1 year of experience and/or training in a clinical laboratory(holding a CLIA Certificate of Compliance/Accreditation)meeting the definition of “high-complexity”.
- Minimum of 3 years of pertinent molecular laboratory experience.
- Minimum of 2 years with aMaster’sor higher.
Level III
Must meet ALL of the following:
- Bachelor’s or higher in medical technology or laboratory science, chemical science, or biological science from an accredited institution.
- Minimum of 3 years of experience and/or training in a clinical laboratory(holding a CLIA Certificate of Compliance/Accreditation)meeting the definition of “high-complexity”.
- Minimum of 2 years with aMaster’sor higher.
- Minimum of 5 years of pertinent molecular laboratory experience.
- Minimum of 3 years with aMaster’sor higher.
- Competent in laboratory automation anddemonstratedlaboratory best practices.
Preferred
- ASCP(MB) certification
- Specialized knowledge and skills: Experience in a clinical, high-throughput environment is preferred.
- Working knowledge of laboratory terminology, equipment, and supplies.
- Competent in laboratory automation anddemonstratedlaboratory best practices.
- Experience working within an electronic Laboratory Information Management System
- Self-motivated and can work independently, with minimal supervision, while also working as part of a team environment in a dynamic organization. Strong interpersonal and communication skills, both written and spoken.
- Experience withAdaptive’sSample Prep or PCR/Sequencing technologies or Methods.
Working Conditions
Jobinvolves working in a laboratory handling human biological specimens. Employees work on assigned shifts which may include late evenings& weekends. Occasional flexibility and willingness to work more than assigned hours is expected.
Possible working shifts include:
- AM shift: Friday - Tuesday 6:00am - 2:30pm
- PM shift: Friday - Monday 12:30pm - 11:00pm
Individualsare required tosit or stand for much of the workday and perform data entry into computer systems.
Compensation
- Level I:$26.87–$40.34per hour
- Level II:$30.24–$45.34per hour
- Level III:$38.17–$57.31per hour
Other compensation elements include
- Equity grant
- Bonus eligible
Interested in this position, but don’t meet all the requirements? Adaptive is committed to building diverse, equitable, and inclusive teams across our organization. Please consider applying even if your experience doesn’t match all the qualifications; you may be the exact candidate we’re searching for!
Adaptive is not currently sponsoring candidates requiring work authorization support for this position.
Adaptive’s posted compensation information includes a base salary (or hourly rate) range and summary of other available total compensation. The base salary range represents a minimum-to-maximum salary (or hourly rate) available to candidates upon extension of offer. Base salary is thoughtfully considered upon offer and is determined through multiple evaluation checks throughout the interview process, including: a candidate’s ability to meet minimum qualifications (skills/experience/education), a candidate’s ability to thoughtfully address preferred qualifications, current market conditions, and internal pay equity. Listed base salary is exclusive of bonus, commission, equity, differential pay, benefits, and other incentives.
Adaptive’s benefits at-a-glance.
Adaptive Biotechnologies is an Affirmitive Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against based on disability. Please refer the "Know Your Rights: Workplace Discrimination is Illegal" Poster for more information. If you’d like to view a copy of the company’s affirmative action plan or policy statement, please email hr@adaptivebiotech.com.
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NOTE TO EMPLOYMENT AGENCIES
Adaptive Biotechnologies values our relationships with our Recruitment Partners and will only accept resumes from those partners who have active agreements with Adaptive. Adaptive Biotechnologies is not responsible for any fees related to resumes that are unsolicited or are received by any employee of Adaptive Biotechnologies who is not a member of the Human Resources team.