Abbott Posted November 6, 2026

Clinical Laboratory Scientist I

Marshfield, Wisconsin, 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.

The Clinical Laboratory Scientist I performs laboratory analyses on clinical specimens using established laboratory procedures within the assigned department or laboratory. Responsibilities include, but are not limited to, specimen processing; performing moderate- and high-complexity testing; establishing, conducting, and documenting quality assurance and quality control activities; maintaining laboratory equipment; and accurately documenting all work performed under the direction of the Laboratory Medical Director. The Clinical Laboratory Scientist I is expected to identify and resolve problems using sound laboratory practices and professional judgment.

Shift: Friday-Monday 6:00am-4:30pm

Essential Duties and Responsibilities

Perform moderate- and high-complexity laboratory tests, procedures, and analyses in accordance with established laboratory standard operating procedures (SOPs).

Perform, review, and document laboratory quality control activities.

Operate, maintain, and troubleshoot laboratory equipment.

Prepare reagents and materials required for laboratory testing.

Identify and troubleshoot routine issues that may affect test performance or laboratory operations.

Achieve and maintain competency in assigned laboratory procedures and tasks.

Assist in training and mentoring new laboratory personnel on current and updated procedures, as needed.

Maintain appropriate inventory levels of laboratory supply to support daily operations.

Participate in the testing, validation, and implementation of new laboratory equipment and procedures.

Maintain high standards of quality by identifying issues that may impact test results, laboratory operations, or employee safety, and communicate concerns to management for resolution.

Manage daily testing responsibilities and project-related activities efficiently and accurately.

Communicate effectively and maintain professional working relationships with employees, managers, and customers.

Participate in quality assurance initiatives and inspection preparation activities.

Receive and apply feedback constructively and professionally.

Participate in continuing education, staff meetings, and professional development activities.

Meet productivity and turnaround time (TAT) expectations.

Collaborate effectively as a member of a team.

Demonstrate flexibility in adapting to changing priorities, tasks, and schedules.

Maintain a high level of attention to detail.

Exhibit strong written and verbal communication skills.

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

Demonstrate adaptability and maintain a positive attitude during organizational and laboratory changes.

Support and comply with all Quality Management System (QMS) policies and procedures.

Maintain regular and reliable attendance.

Foster an inclusive and respectful work environment.

Work the assigned schedule and overtime as required.

Physical and Environmental Requirements

Ability to lift up to 40 pounds for approximately 25% of the workday.

Ability to sit for approximately 50% and stand for approximately 50% of the workday.

Ability to work on a computer, tablet, or other electronic device and perform typing for approximately 75% of the workday.

Ability to perform technical laboratory work for up to 95% of the workday and administrative duties for up to 5%.

Ability to grasp, pinch, turn, and reach above shoulder height.

Ability to use various laboratory instruments and perform repetitive motions.

Ability to comply with all required personal protective equipment (PPE) standards.

Ability to work safely in environments that may include exposure to biological specimens, hazardous materials, moving equipment parts, lasers, heating and cooling elements, and high-speed centrifuges.

Ability to use near vision to examine specimens and laboratory materials.

Adhere to laboratory safety requirements and maintain patient confidentiality and data security at all times.

Travel between company sites may be required.

Minimum Qualifications

Associate degree in Laboratory Science (Chemical or Biological Science) or Medical Laboratory Technology from an accredited institution, or equivalent laboratory training and experience.

Authorization to work in the United States without employer sponsorship.

Demonstrated ability to perform the essential functions of the position, with or without reasonable accommodation.

Working knowledge of applicable local, state, and federal laboratory regulations.

Preferred Qualifications

Bachelor's degree in chemical, Biological, Clinical Laboratory Science, or Medical Technology from an accredited institution.

Experience with molecular biology principles and laboratory techniques.

Knowledge of laboratory validation processes and quality systems.

Equal Employment Opportunity

We are an Equal Employment Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other characteristic protected by applicable law.

The base pay for this position is $20.50 – $41.00 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
Marshfield, Wisconsin, 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 1458 comparable Quality roles across 143 biopharma companies.

1458Comparable roles tracked
1336Currently active
143Companies hiring similar roles
53Countries represented

Salary context

256 of 1458 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 · QC Lab Technician (Lilly Contractor - Fixed Term) · Lilly $13/hr – $29/hr (≈ $26,998–$60,507/yr)
Highest disclosed · VP, Quality Assurance · City Therapeutics $340,000/yr – $360,000/yr
Peer group range $43,753 – $350,000 (median $120,250)

Where these roles are based

Top locations among the 1458 comparable roles

United States595
Ireland87
France71
Germany68
China66
India56

+ 47 more countries

Seniority mix

712 of 1458 peers have a known seniority level

Manager217
Senior166
Intern/Fellow/Postdoc100
Associate68
Associate Director46
Director45
Principal38
Senior Director25
Executive/VP7

Therapeutic area mix

2 of 1458 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease2

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 Lebanon, Indiana, United States of America Principal
Same function Same country
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

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.

Or follow a whole field: get every new Quality job in the United States, and choose locations and companies.

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%
Principal Scientist GMP Environmental Monitoring Lilly Medicine Foundry
Lilly · Lebanon, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
40%
Senior Manager, Clinical Quality Assurance
AbbVie · North Chicago, IL · Manager
Function Therapeutic area Seniority Country
40%
Senior Manager, Quality Assurance
Gilead Sciences, Inc. · Foster City, United States · Manager
Function Therapeutic area Seniority Country
40%
Principal QA Validation Specialist, Fill Finish
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Principal
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.