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Production Chemist I

2 months ago

Pomona, United States Abbott Laboratories Full time

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 114,000 colleagues serve people in more than 160 countries.

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.
  • Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
  • 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

Abbott Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry-leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.

The position of Production Chemist I – Biologics is within our Toxicology Business Unit located in Pomona, CA. Under 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.  In this role, you will help manufacture and evaluate biologics for use in Drugs of Abuse (DOA) immunoassays. 

This job description will be reviewed periodically and is subject to change by management.

Shift

Monday to Friday

8:30 am-5:00 pm

What You’ll Work On

  • Follows SOP and batch records for manufacturing antibodies and biologics reagents for HEIA, SEFRIA, and LFIA diagnostic product platforms.
  • Performs purification of antibodies for HEIA, SEFRIA, and LFIA using Immobilized Metal Affinity Chromatography (IMAC) or protein G purification.
  • Performs in-process functional testing and characterization of antibodies for HEIA and SEFRIA platforms using absorbance readers and Sodium Dodecyl Sulfate–polyacrylamide gel electrophoresis (SDS-PAGE)
  • Assists in qualification read and understand Standard Operating Procedures (SOPs) related to job functions to carry out production tasks in support of manufacturing goals and objectives.
  • Manufacture all products via Batch Records and Standard Operation Procedures (SOPs) following the guidelines for Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) by the Quality System.
  • Operate laboratory equipment safely, as trained and directed, by 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.
  • Creation of item specifications or other documentation in the manufacturing process.
  • Operate moderately complex laboratory equipment and perform routine calibrations and maintenance.
  • Manufacture complex reagents and media solutions as directed, following established guidelines and procedures.
  • Perform component and material evaluations using established testing methods.
  • Follow all safety guidelines, manufacturing policies, and procedures.  Operate under an established Quality Management System and ISO compliance.
  • Participate in product/process troubleshooting and validations
  • Carry out functions that may require multiple-task coordination
  • Understands and is aware of the quality consequences that 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, validation, manufacturing, and testing activities.
  • 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.
  • Carries out duties in compliance with established business policies
  • Other duties as assigned, according to the changing needs of the business.

Required Qualifications

  • BA or BS in Chemistry, Chemical Engineering, Microbiology, Immunology, Physical, or Biological Sciences.
  • Zero to two years experience in a biologics production laboratory or chemistry laboratory.
  • Strong verbal and written communication skills.
  • Ability to follow detailed instructions, maintain accurate records and notes, and carry out assignments in a thorough, conscientious fashion while adhering to safe laboratory practices.
  • Knowledge and ability to use MS Office (Outlook, Word, Excel, PowerPoint).
  • Knowledge or experience with microbial fermentation/bioprocessing and the respective laboratory equipment and operation.
  • Knowledge or experience with antibody purification: Immobilized Metal Affinity Chromatography (IMAC) purification or Protein G purification.
  • Able to carry out production tasks following established guidelines and summarize results accurately.

PREFERRED QUALIFICATIONS:

  • Demonstrate problem-solving and troubleshooting skills.
  • Knowledge or experience with bioprocessing software (EZ control, BioExpert, Lucullus, BugEye Biomass Detector).
  • Knowledge or experience with Sodium Dodecyl Sulfate–polyacrylamide gel electrophoresis (SDS-PAGE).
  • Knowledge or experience with the evaluation of antibodies on various immunoassay platforms.
  • 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.
  • Process-orientated, logical, analytical, meticulous, highly organized, and able to analyze data & implement solutions.
  • Proven ability to work effectively within a team environment while satisfying individual responsibilities and objectives.

* Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.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 www.abbott.com, on Facebook at www.facebook.com/Abbott, and Twitter @AbbottNews.



The base pay for this position is $21.55 – $43.15 per hour. In specific locations, the pay range may vary from the range posted.