Sr. Analytical Chemist - IVD Reagents and Small Molecules at Abbott

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:

Sr. Analytical Chemist – IVD Reagents and Small Molecules 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

At Molecular Diagnostics, we realize the potential of personalized care as the laboratory’s most trusted and preferred source for molecular diagnostic solutions. We are a division of Abbott Laboratories, a global, diversified healthcare innovator with a legacy of pioneering work in medical diagnostics.

Position: Sr.Analytical Chemist – IVD Reagents and Small Molecules Location:Molecular Diagnostics Business Unit, Des Plaines, Illinois

AMD Molecular is recruiting for an Sr.Analytical Chemist – IVD Reagents and Small Molecules with deep expertise in ion chromatography (IC), high‑performance liquid chromatography (HPLC), and atomic absorption (AA) spectroscopy to support the development and validation of reagents, raw materials, and small molecules—including oligonucleotides and nucleic‑acid probes—used in in vitro diagnostic (IVD) assays. Proficiency in LC‑MS for detailed oligonucleotide and small‑molecule characterization is also preferred.

What You’ll Work On

1.

Analytical Method Development & Testing:

• Develop, optimize, and validate analytical methods using IC, HPLC, AA, and LC‑MS to support characterization of raw materials, reagents, oligonucleotides, nucleic‑acid probes, and other small molecules.
• Perform routine and non‑routine testing to ensure compliance with specifications for raw materials, intermediates, and finished reagents.
• Design and execute analytical experiments supporting IVD assay development, small‑molecule characterization, formulation optimization, and stability studies.

2.

Instrument Ownership & Troubleshooting:

• Operate, maintain, and troubleshoot analytical instrumentation, including IC and HPLC systems equipped with UV, conductivity, and mass‑spectrometry detection.
• Maintain instrument readiness, calibration, and associated documentation in accordance with GMP/GLP requirements.

3. Documentation, Quality, & Regulatory Compliance

• Prepare and review validation protocols, test methods, technical reports, SOPs, and analytical sections of regulatory submissions.
• Ensure data integrity and compliance with 21 CFR 820, ISO 13485, and applicable FDA/ICH/USP guidelines.
• Generate, analyze, and interpret complex analytical data sets to support product development, investigations, and quality decision‑making

4. Cross‑Functional Support & Investigation Leadership

• Lead analytical investigations, including root‑cause analysis, and provide technical recommendations for corrective and preventive actions (CAPA).
• Collaborate with R&D, Quality, Manufacturing, and other stakeholders to support product development, process validation, and material assessments.
• Serve as a subject‑matter expert in analytical methodologies, providing technical guidance to cross‑functional teams.

5.

Training & Mentorship:

• Train and mentor junior staff in analytical techniques, instrument best practices, and data‑integrity requirements.

Required Qualifications

• Master's or Ph.D. in Analytical Chemistry, Chemistry, Biochemistry, or related field; Bachelor's with significant experience considered.
• 5+ years of analytical method development and validation experience in a regulated environment.
• Demonstrated expertise in IC, HPLC, AA, and LC‑MS for characterization of oligonucleotides, nucleic‑acid probes, and other small molecules.
• Familiarity with complementary material characterization techniques (e.g., UV‑Vis, Karl Fischer, TOC).
• Experience with GMP/GLP, method lifecycle, and regulatory documentation.
• Strong statistical foundation for method validation.

Preferred

• Proficiency in LC‑MS for detailed oligonucleotide and small‑molecule characterization is also preferred.
• Experience with biologics, enzymes, or complex matrices.
• Knowledge of data integrity principles and electronic laboratory systems (e.g., LIMS, ELN).
• Knowledge of design control and risk management in the context of IVD product development.
• Prior experience supporting 510(k) or PMA submissions is a plus.

Apply Now

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 on Twitter @AbbottNews.

The base pay for this position is

$78,000.00 – $156,000.00

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

JOB FAMILY:

Manufacturing

DIVISION:

AMD Molecular

LOCATION:

United States > Des Plaines : DP01

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Not specified

MEDICAL SURVEILLANCE:

Not Applicable

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), 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