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Salary
$40k – $82k per year
Location
In office (Redwood City)
Seniority
Middle · 2+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Abbott is an American healthcare company founded in 1888 by a Chicago physician who began making precise doses of alkaloid medicines for his own patients. It now operates four large businesses: diagnostics, including the point-of-care and molecular testing that scaled during the pandemic, medical devices spanning cardiac rhythm, structural heart, neuromodulation and continuous glucose monitoring, nutrition brands such as Similac and Ensure, and established pharmaceuticals sold mainly in emerging markets. The company is headquartered in North Chicago, Illinois, and separated its research-based drug business as AbbVie in 2013.
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:

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: Tuesday-Saturday, 9:00am - 5:30pm

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.
  • 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.
  • Authorization to work in the United States without sponsorship

Preferred Qualifications

  • Associates Degree in Science, Health Science or related field as outlined in the essential duties.
  • Experience in laboratory training and training programs.
  • Demonstrated ability to write and update procedures.

The base pay for this position is

$20.75 - $41.45/hour

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

JOB FAMILY:

Operations Quality

DIVISION:

ONCO Cancer Diagnostics

LOCATION:

United States > Redwood City : 501 Galveston Dr

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

No

MEDICAL SURVEILLANCE:

No

SIGNIFICANT WORK ACTIVITIES:

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), Lift, carry, push or pull weights of more than 20 pounds/9 kilos on a regular/daily basisAbbott 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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
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