Abbott Posted September 23, 2026

Pre-Analytical Laboratory Technician II

Redwood City, California, United States FULL_TIME
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Abbott is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

Position Overview

The Pre-Analytical Laboratory Technician II is responsible for preparing samples for analysis, recording, and/or verifying patient’s information. This role is primarily responsible for performing duties related to accessioning, sample management, problem resolution, data entry, and specimen storage with high degree of proficiency. A successful candidate would be expected to have the ability to swiftly pick up new laboratory process that they are trained in due to experience gained in previous laboratory roles. Potential candidates should be able to demonstrate that they have good documentation practices (GDP) knowledge.

Shift: Monday-Friday: 11am-7:30pm PST

Essential Duties Include, but are not limited to, the following:

Perform laboratory tasks, as assigned.

Clean and organize common lab areas and take responsibility for all housekeeping tasks being completed on time.

Receive, sort, and unpack incoming samples regularly.

Unpack, log and track incoming samples using specified software regularly.

Perform administrative duties required for incoming samples; including, but not limited to scan needed paperwork, such as pathology reports and requisitions and file physical paperwork per required procedures.

Perform order entry and order processing such as in lieu of; including, but not limited to reviewing patient demographics and sample collection.

Evaluate insurance and verify billing information.

Transcribe relevant medical information from pathology reports or other associated documents such as sample IDs, number or malignant cores, and tumor size.

Perform sample accessioning; including, but not limited to, verification of patient demographics, sample ID, and sample labeling.

Utilize laboratory information system (LIMS), to review, enter sample information and print required work lists.

Perform and record equipment maintenance.

May assist in training.

Follow and assess established health and safety procedures.

Adhere and perform risk assessments as well as understand, train, and enforce safety regulations.

Comply with ISO 15189 and QMS.

Record data adhering to GDP, strictly follow procedures and proactively raise quality concerns events, when necessary.

Maintain standard operating procedures (SOPs).

May lead and participate in process improvement activities planned by management and/or engineers.

Contribute to overall team goals while still maintaining individual output.

Foresee issues and overcomes obstacles to completing tasks or assignments. 1 May not be reproduced nor disseminated outside of Exact Sciences & its subsidiaries without permission

Participate in continuing education and staff meetings.

Performed all assigned tasks under the supervision of designee.

Ability to work in a fast pace and changing environment.

Flexible and quickly adaptable to changing priorities.

Ability to consistently display a positive and patient attitude and extend respect and courtesy toward management and peers alike.

Ability to troubleshoot and develop critical thinking skills.

Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.

Support and comply with the company’s Quality Management System policies and procedures.

Maintain regular and reliable attendance.

Ability to act with an inclusion mindset and model these behaviors for the organization.

Ability to work designated schedule.

Ability to work nights and/or weekends as needed.

Ability to work overtime as needed.

Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 85% of a typical working day.

Ability to work seated for approximately 75% of a typical workday.

Ability to work standing for approximately 25% of a typical workday.

Ability to lift to 10 pounds for approximately 10% of a typical workday.

Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height.

Considerable periods of time may be spent concentrating and or analyzing data.

Ability to comply with any applicable personal protective equipment requirements.

Ability to use various types of laboratory equipment; including microscopes, microtomes, blades, strainers, and pipettes for extended periods of time.

May perform repetitious actions using lab tools.

Ability to use near vision to view samples at close range.

May be exposed to hazardous materials, tissue specimens, and instruments with moving parts, lasers, heating and freezing elements, and high-speed centrifugation.

Ability and means to travel between Redwood City locations.

Minimum Qualifications

High School Diploma or General Education Degree (GED).

2+ years of experience working in a laboratory maintaining sample integrity by following procedures and protocols.

Professional working knowledge with using laboratory information management systems.

Advanced computer skills to include email usage.

Proficient with Microsoft Office Word, Excel and Outlook.

Demonstrated ability to perform the Essential Duties of the position with or without accommodation.

The base pay for this position is $17.00 – $34.00 per hour. In specific locations, the pay range may vary from the range posted.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Redwood City, California, United States
Employment type
FULL_TIME

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 1369 comparable Quality roles across 143 biopharma companies.

1369Comparable roles tracked
1241Currently active
143Companies hiring similar roles
52Countries represented

Salary context

230 of 1369 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · QA - Stat Sort Specialist · Lilly $18/hr – $35/hr (≈ $37,482–$72,592/yr)
Highest disclosed · Vice President, Quality Assurance - GMP · Exelixis Inc $315,500/yr – $366,500/yr
Peer group range $55,037 – $341,000 (median $129,052)

Where these roles are based

Top locations among the 1369 comparable roles

United States553
Ireland82
China62
France58
Germany51
India50

+ 46 more countries

Seniority mix

625 of 1369 peers have a known seniority level

Manager183
Senior166
Intern/Fellow/Postdoc73
Associate68
Associate Director35
Director35
Principal30
Senior Director28
Executive/VP7

Therapeutic area mix

1 of 1369 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same country
40%similar
AbbVie North Chicago, IL Director
Same function Same country
40%similar
AbbVie North Chicago, IL Manager
Same function Same country
40%similar
Gilead Sciences, Inc. La Verne, United States
Same function Same country
40%similar
Gilead Sciences, Inc. La Verne, United States Senior
Same function Same country
40%similar
Gilead Sciences, Inc. Foster City, United States Manager
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Advisor, Physicochemical Properties and Compound Quality
Lilly · Indianapolis, Indiana, United States of America · Associate
Function Therapeutic area Seniority Country
40%
Senior Manager, Clinical Quality Assurance
AbbVie · North Chicago, IL · Manager
Function Therapeutic area Seniority Country
40%
Sr. Quality Assurance Specialist
Gilead Sciences, Inc. · La Verne, United States · Senior
Function Therapeutic area Seniority Country
40%
Senior Manager Quality Assurance, Medical Device (Sustaining)
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.