Clinical Laboratory Scientist I

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.

Job description

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/hour

In specific locations, the pay range may vary from the range posted.

Job family Operations Quality

Divisione ONCO Cancer Diagnostics

Sede di lavoro United States > Marshfield : Mill Creek Campus

Sedi di lavoro ulteriori

Turni Standard

Viaggiare No

Controllo medico No

Attività lavorative significative Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday), Routine work with chemicals, Work in a clean room environment

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf