Abbott Posted October 10, 2026

Sr. Clinical Lab Associate - 2nd 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 Lab Associate, Specimen Processing is responsible for performing the day-to-day operations of the Specimen Processing Department; including, but not limited to, lab productivity and process line support, exception handling, lab maintenance, and lab logistics. Tasks may include but are not limited to: lead production workflow and automation troubleshooting, advanced sample problem resolution, sample storage audits and troubleshooting, advanced automation maintenance, monitor production reports and goal progress, support employee feedback and redirection, support the review and editing of standard operating procedures, lead team meetings.

The Senior Clinical Lab Associate, Specimen Processing follows all Laboratory policies and procedures and maintains accurate data reporting practices to ensure consistent and diligent execution of Specimen Processing. This role supports the mission and vision of Exact Sciences Laboratories and shares the responsibility of ensuring the Specimen Processing department operates effectively. The function of this position is performed under the guided direction of the Specimen Processing Supervisor or designee.

Shift: Tues - Fri, 2p - 1130p

Essential Duties

include but are not limited to the following:

Perform primary responsibilities listed below completely, timely and accurately: Support and comply with the company’s Quality Management System policies and procedures.

Maintain documentation of problems and problem resolutions following Good Documentation Practices (GDP).

Work with leadership to develop department goals that align with organizational priorities.

Work with leadership to identify and progress on individual development goals that align with organizational priorities.

Support operational initiatives including, but not limited to, quality and process improvements, SOP development, department inspections and audits.

Assist and support the Clinical Lab Training Department; including, but not limited to, reviewing department specific training materials, identifying additional training needs/resources, and providing training, as needed.

Complete all mandatory training assignments and annual competencies within established timelines.

Handle and dispose of all specimens following standard precautions and applicable safety policies.

Understand and comply with all lab and safety regulations.

Support employee engagement initiatives and activities to maintain and improve team morale.

Communicate and manage change effectively.

Meet performance and behavior expectations listed below: Exemplify the core values of Integrity, Teamwork, Accountability, Quality , and Innovation at all times.

Self-motivation with a results-driven approach.

Maintain a high level of professionalism in written and verbal communications.

Act with an inclusion mindset and model these behaviors for the organization.

Maintain regular and reliable attendance.

Demonstrate the necessary skills and abilities: Ability to work in a fast-paced team environment, adapt to changing workload and circumstances effectively and respond to new information quickly.

Strong critical thinking skills with the ability to make decisions in a fast-paced environment.

Ability to communicate effectively with all levels of the organization through both verbal and written communication.

High level of listening skills and attention to detail with strong organizational and prioritization skills.

Ability to flex hours and work nights and/or weekends as needed to support the success of ES Labs.

Ability to work overtime, as needed.

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

Ability to comply with any applicable personal protective equipment requirements.

Ability to perform repetitive motions.

Understand potential exposure to hazardous materials, tissue specimens and instruments with moving parts, heating and freezing elements.

Tolerate the handling of bodily fluids and solids (e.g., blood, urine and feces).

Ability and means to travel to and work at all other sites within the same city, as needed.

Minimum Qualifications

High School Degree/General Education Diploma.

Must be 18 years of age or older.

2+ years of experience working in a laboratory, medical or high throughput environment.

1+ year of experience leading, mentoring and/or coaching others with or without direct reports.

General knowledge and understanding of CAP, GLP, GDP, CLIA, New York State Department of Health (NYSDOH), and HIPAA.

Intermediate knowledge and experience using Internet navigation, email, Microsoft Office Suite.

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

Associate degree or Bachelor’s degree in Life Sciences, Physical Sciences, or related field.

3+ years of experience in a clinical laboratory or 2.5 years in Cologuard Clinical Lab.

1+ year of experience leading a team of direct reports or 2+ years of experience leading, mentoring and/or coaching others without direct reports.

Experience in troubleshooting automation and performing instrument maintenance.

Lean experience (Kaizen, Kanban, root cause analysis, countermeasure implementation, etc.).

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
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
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60%similar
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60%similar
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Amgen Inc. Thousand Oaks, United States Senior
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60%similar
Novo Nordisk West Lebanon, United States Senior
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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.