Pre-Analytical Laboratory Technician II

Abbott•Redwood City, CA

4d•$21 - $41•Onsite

About The Position

The Pre-Analytical Laboratory Technician II prepares samples for analysis and records or verifies patient information. The role focuses on accessioning, sample management, problem resolution, data entry, and specimen storage, performed with a high degree of proficiency. The successful candidate can quickly learn new laboratory processes and demonstrates knowledge of good documentation practices (GDP). The position is part of Abbott Cancer Diagnostics (ONCO), which develops tests for cancer prevention, earlier detection, and treatment guidance. The technician performs assigned laboratory and administrative work, follows established procedures and safety requirements, supports quality systems, and contributes to team and process-improvement goals. Work is performed under the supervision of a designee. The stated schedule is Monday through Thursday and Saturday, 9:00 a.m.–5:30 p.m. PST. The role is located in Redwood City, California, and requires the ability and means to travel between Redwood City locations.

Requirements

High school diploma or General Education Degree (GED).
At least 2 years of experience working in a laboratory while maintaining sample integrity by following procedures and protocols.
Professional working knowledge of laboratory information management systems.
Advanced computer skills, including email usage.
Proficiency with Microsoft Word, Excel, and Outlook.
Demonstrated ability to perform the essential duties with or without accommodation.
Ability to work in a fast-paced, changing environment and adapt quickly to changing priorities.
Ability to demonstrate a positive and patient attitude and treat management and peers with respect and courtesy.
Ability to troubleshoot and use critical-thinking skills.
Ability to work on a mobile device, tablet, or computer and type for approximately 85% of a typical workday.
Ability to work seated for approximately 75% and standing for approximately 25% of a typical workday.
Ability to lift up to 10 pounds for approximately 10% of a typical workday.
Ability to grasp with both hands, pinch with thumb and forefinger, turn with the hand or arm, and reach above shoulder height.
Ability to spend considerable periods concentrating on or analyzing data.
Ability to comply with applicable personal protective equipment requirements.
Ability to use laboratory equipment, including microscopes, microtomes, blades, strainers, and pipettes, for extended periods; may perform repetitive actions using laboratory tools.
Ability to use near vision to view samples at close range.
Ability and means to travel between Redwood City locations.
May be exposed to hazardous materials, tissue specimens, and instruments with moving parts, lasers, heating and freezing elements, and high-speed centrifugation.

Responsibilities

Perform assigned laboratory tasks.
Clean and organize common laboratory areas and complete housekeeping tasks on time.
Receive, sort, unpack, log, and track incoming samples using specified software.
Scan and file paperwork related to incoming samples, including pathology reports and requisitions, according to required procedures.
Perform order entry and processing, including reviewing patient demographics and sample collection information.
Evaluate insurance and verify billing information.
Transcribe relevant medical information from pathology reports and related documents, such as sample IDs, number of malignant cores, and tumor size.
Accession samples by verifying patient demographics, sample IDs, and sample labeling.
Use the laboratory information system (LIMS) to review and enter sample information and print required work lists.
Perform and record equipment maintenance.
Assist with training when needed.
Follow and assess established health and safety procedures; perform risk assessments and understand, train, and enforce safety regulations.
Comply with ISO 15189 and the Quality Management System (QMS).
Record data according to GDP, follow procedures, and proactively raise quality concerns when necessary.
Maintain standard operating procedures (SOPs).
Lead and participate in process-improvement activities planned by management and/or engineers when needed.
Contribute to team goals while maintaining individual output, anticipate issues, and overcome obstacles to completing work.
Participate in continuing education and staff meetings.
Complete assigned tasks under the supervision of a designee.
Support company mission and values, QMS policies and procedures, regular and reliable attendance, and an inclusive workplace.
Work the designated schedule and nights, weekends, or overtime as needed.