Abbott Posted September 30, 2026

Sr. Clinical Laboratory Scientist - 3rd Shift

Madison, Wisconsin, United States FULL_TIME
Quality Senior
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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 Senior Clinical Laboratory Scientist will be responsible for performing moderate and high complexity laboratory testing on patient specimens, interpreting and reporting patient results, performing quality control and quality assurance procedures, assisting Laboratory Leadership with advanced laboratory duties, and complying with all applicable local, state, and federal laboratory requirements. The Senior Clinical Laboratory Scientist will continually display excellent initiative in all aspects of their work, contribute to projects and discussions in addition to daily laboratory testing and consistently performing to high standards.  Leadership is demonstrated in technical troubleshooting of laboratory instrumentation and processes as well as laboratory quality improvements, health and safety, and training of laboratory staff.

Shift: Tues - Fri, 10p - 730a

Essential Duties

include but are not limited to:

Perform moderate and highly complex laboratory tests, procedures, and analyses according to the laboratory’s standard operating procedures with minimal supervision.

Perform, review, and document laboratory quality control procedures.

Identify potential problems, determine potential solutions, and take appropriate action in order to maintain a high level of quality in test processes and results.

Achieve and maintain competency on laboratory tasks.

Participate in research, validation, and/or implementation of new procedures and/or technologies.

Maintain stringent standards for quality, by identifying, investigating, correcting, and documenting any issues which might adversely impact the quality of test results and/or employee safety, and communicating these to the appropriate management representatives as necessary for resolution.

Determine appropriate time allocation between daily test processing needs and project needs in a high quality, efficient and effective manner with minimal direction.

Demonstrate and maintain effective communication with internal employees, managers, customers, and cross-functional teams.

Model behaviors that promote high productivity, quality and maintaining TAT.

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

Demonstrate adaptability by embracing changes in the laboratory with a positive attitude.

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

Maintain regular and reliable attendance.

Act with an inclusive mindset.

Work a designated schedule.

Ability to work overtime, as needed.

Ability to lift up to 40 pounds for approximately 25% of a typical working day.

Ability to work seated for approximately 50% of a typical working day. Ability to work standing for approximately 50% of a typical working day.

Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 75% of a typical working day.

Ability to perform technical work up to 80% of a typical working day and administrative work up to 20% of a typical working day.

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

Ability to use various types of laboratory equipment and perform repetitive motions.

Ability to comply with any applicable personal protective equipment requirements.

Comply with safety and hazard regulations as outlined in the clinical laboratory safety manual.

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

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

Observe principles of data security and patient confidentiality. Maintain ethical standards in the performance of testing and in interactions with patients, co-workers, and other health care professionals.

Travel between Exact Sciences sites may be required.

Perform job duties as expected of a Clinical Laboratory Scientist.

Perform training and competency tasks with laboratory personnel on current and new procedures.

Provide leadership in daily activities as a shift senior scientist.

Assist the laboratory supervisors including, but not limited to, writing, and reviewing procedures, documents, and forms, and assisting in developing the troubleshooting and decision-making skills of the Clinical Laboratory Scientists.

Oversee the activities and provide guidance and constructive feedback to clinical laboratory scientists I and II.

Ability to recognize deviations from the accepted practice and perform deep root cause analysis.

Professional demeanor and behavior in all work-related interactions.

Ability to respond to stakeholder requests in a professional and timely manner.

Minimum Qualifications

Associate degree in a laboratory science (chemical or biological science) or medical laboratory technology from an accredited institution or equivalent laboratory training and experience as defined: 60 semester hours or equivalent from an accredited institution that, at a minimum, includes either 24 semester hours of medical laboratory technology courses, OR 24 semester hours of science courses that include six semester hours of chemistry, six semester hours of biology, and 12 semester hours of chemistry, biology or medical laboratory technology in any combination.

3+ years of high complexity clinical testing experience in a clinical laboratory setting.

Demonstrated strong professionalism and leadership skills.

Demonstrated intermediate level project management skills.

Demonstrated strong technical skills and professional working knowledge of job industry.

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

Authorization to work in the United States without sponsorship.

Preferred Qualifications

Bachelor's degree in a chemical, biological or clinical laboratory science or medical technology from an accredited institution. For degree not in those listed above:  90 semester hours which must include 16 semester hours in chemistry (6 of which must be in inorganic chemistry); 16 semester hours in biology courses and 3 semester hours of math.

Certification from one of the nationally recognized certification agencies such as ASCP or state licensure that has been determined to be equivalent.

Experience with laboratory automation and laboratory information systems.

Experience in molecular biology techniques and principles.

The base pay for this position is $26.50 – $53.00 per hour. In specific locations, the pay range may vary from the range posted.

Job details

Seniority
Senior
Function
Quality
Therapeutic area
Not listed
Location
Madison, 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 230 comparable Senior Quality roles across 59 biopharma companies.

230Comparable roles tracked
216Currently active
59Companies hiring similar roles
29Countries represented

Salary context

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

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Quality Control Chemist, Senior (Data Review) Mid Shift · Merck KGaA $25/hr – $39/hr (≈ $52,000–$81,120/yr)
Peer group range $66,560 – $208,845 (median $131,050)

Where these roles are based

Top locations among the 230 comparable roles

United States121
Ireland15
China10
India9
Singapore9
Spain8

+ 23 more countries

Seniority mix

230 of 230 peers have a known seniority level

Senior165
Associate Director35
Principal30

Therapeutic area mix

0 of 230 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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.

60%similar
Gilead Sciences, Inc. La Verne, United States Senior
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Senior
Same function Same seniority Same country
60%similar
JuN - Seattle Dexter Seattle 400 Dexter, United States Senior
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60%similar
Amgen Inc. Thousand Oaks, United States Senior
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60%similar
Novo Nordisk West Lebanon, United States Senior
Same function Same seniority Same country
60%similar
Biogen Research Triangle Park, United States Senior
Same function Same seniority 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.

60%
Sr. Quality Assurance Specialist
Gilead Sciences, Inc. · La Verne, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Associate Quality Assurance
Amgen Inc. · Thousand Oaks, United States · Senior
Function Therapeutic area Seniority Country
60%
Sr Associate I, Quality Control Microbiology
Biogen · Research Triangle Park, United States · Senior
Function Therapeutic area Seniority Country
60%
Sr. Associate III, Compliance
Biogen · Research Triangle Park, United States · Senior
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.