Production Chemist I

United States - California - Pomona April 24, 2026 Full Time Workday
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 115,000 colleagues serve people in more than 160 countries.

     

JOB DESCRIPTION:

Position Title

Production Chemist I

Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

  • Career development with an international company where you can grow the career you dream of.

  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

  • An excellent retirement savings plan with a high employer contribution.

  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

The position of Production Chemist I is within our Toxicology Business Unit located in Pomona, California.   

Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments, and informatics systems is often the first step in patient care decision-making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers. 

What You’ll Work On

  • Adhere to laboratory safety rules

  • Read and understand Standard Operating Procedures (SOPs) related to job functions

  • Perform the daily, weekly, monthly, and yearly maintenance of laboratory equipment and maintain maintenance logbooks

  • Manufacture all products via Batch Records and/or Standard Operation Procedures (SOPs) following the guidelines for Good Manufacturing Practice (GMP) in accordance with the Quality System

  • Manufacture antibody solutions, drug positive solutions, enzyme-conjugate solutions, EIA calibrators and controls and reagents

  • Perform a variety of analytical EIA in-process testing

  • Perform daily temperature monitoring

  • Carry out production tasks in support of manufacturing goals and objectives

  • Participates in Lean Activities

  • Operate laboratory equipment safely, as trained and directed, in accordance with established practices

  • Maintain records and notebooks as directed in a neat, thorough and accurate manner. Perform required data entry on company planning and materials management system. Report results to supervisor

  • Maintain a neat and organized workplace. Ensure materials are appropriately labeled, approved for use and in enough quantity to complete required tasks

  • Recommend and participate in document revisions to ensure accurate BOM's process descriptions

  • Recommend and participate in document revisions to ensure accurate NCMR and deviations

  • Perform complex simple formulations, component and material evaluations, equipment calibrations and maintenance

  • Ability to work overtime and/or on weekends

  • Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities

  • Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. 

  • Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices; build productive internal/external working relationships

  • Other duties as assigned, according to the changing needs of the business

Required Qualifications

  • BA or BS in Chemistry or Biological Sciences

  • 0 to 2 (or more) years’ experience in laboratory environment

  • Strong verbal and written communication skills

  • Ability to follow detailed instructions, maintains accurate records and notes, and carries out assignments in a thorough, conscientious fashion while adhering to safe laboratory practices

Preferred Qualifications

  • Knowledge of a variety of lab equipment and their operation is preferred

  • Demonstrate problem-solving and troubleshooting skills

  • Process orientated, Logical, analytical, meticulous, highly organized and able to analyze data & implement solutions

  • Ability to work in a team environment while satisfying individual responsibilities and objectives.

  • Knowledge and ability to use MS Office and other manufacturing systems

  • Adaptable and willing to take on multiple new tasks and responsibilities

  • Independent collaborative self-starter with the ability to make appropriate quality-related decisions in real time

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: https://abbottbenefits.com/

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.

     

The base pay for this position is

$22.55 – $45.15/hour

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

     

JOB FAMILY:

Operations Quality

     

DIVISION:

TOX ARDx Toxicology

        

LOCATION:

United States > Pomona : 829 Towne Center Drive

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Standard

     

TRAVEL:

No

     

MEDICAL SURVEILLANCE:

No

     

SIGNIFICANT WORK ACTIVITIES:

Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day), Lift, carry, push or pull weights of more than 20 pounds/9 kilos on a regular/daily basis, 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
Apply on company site

How to Get Hired at Abbott Laboratories

  • Create your Abbott-specific Workday profile at abbott.wd5.myworkdayjobs.com and complete every field — including skills and certifications — so recruiters can find you even for unlisted roles
  • Rewrite your resume for each Abbott application using the exact regulatory and technical terminology from the job posting, such as 'CAPA,' 'Design Controls,' 'GMP,' and the specific product platform mentioned
How to apply to Abbott Laboratories

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