Manufacturing Chemist (QC) – High Volume Production, Benefits

🏢 Abbott Laboratories📍 Naperville, IL, United States💼 Full-Time💻 On-site🏭 Pharmaceuticals and Diagnostics💰 70000-95000 per year

About the Company

Abbott Laboratories is a global healthcare leader committed to helping people live fuller lives through the power of health. With a portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines, Abbott serves people in more than 160 countries. We are driven by a mission to create breakthrough products that improve people’s health and well-being, from innovative solutions in cardiovascular care to life-changing technologies in diabetes management. Join our dedicated team in Naperville, IL, where we relentlessly pursue scientific excellence to make a lasting impact on global health.

Job Description

We are seeking a highly motivated and detail-oriented Manufacturing Chemist (QC) to join our high-volume production facility in Naperville, Illinois. In this critical role, you will be responsible for performing a variety of quality control tests on raw materials, in-process samples, and finished products to ensure compliance with stringent quality standards and regulatory requirements. This position requires a strong understanding of analytical chemistry principles, meticulous attention to detail, and the ability to work effectively in a fast-paced manufacturing environment. The successful candidate will play a vital role in maintaining product integrity and safety, contributing directly to Abbott’s commitment to delivering high-quality healthcare solutions.

Key Responsibilities

  • Execute routine and non-routine analytical testing on raw materials, in-process intermediates, and finished goods using a range of laboratory instrumentation (e.g., HPLC, GC, UV-Vis, FTIR, titrators).
  • Interpret and analyze test results, ensuring accuracy and adherence to established specifications and standard operating procedures (SOPs).
  • Troubleshoot analytical instrumentation and methods, performing minor repairs and calibrations as needed.
  • Document all testing activities, results, and observations accurately and thoroughly in laboratory notebooks and electronic systems.
  • Investigate out-of-specification (OOS) results, deviations, and non-conformances, participating in root cause analysis and corrective action implementation.
  • Maintain laboratory equipment in good working order, performing preventative maintenance and ensuring calibration schedules are met.
  • Assist in the development and validation of new analytical methods and the transfer of existing methods.
  • Contribute to continuous improvement initiatives within the QC laboratory and manufacturing operations.
  • Ensure strict compliance with GMP, GLP, EHS, and other relevant regulatory guidelines and company policies.
  • Collaborate cross-functionally with production, R&D, and regulatory affairs teams to support manufacturing operations.

Required Skills

  • Bachelor's degree in Chemistry, Biochemistry, or a related scientific field.
  • 3+ years of experience in a Quality Control or Analytical Chemistry laboratory within a manufacturing environment (pharmaceutical, medical device, or similar highly regulated industry preferred).
  • Proficiency in operating and troubleshooting analytical instruments such as HPLC, GC, UV-Vis, and FTIR.
  • Strong understanding of cGMP, GLP, and other relevant regulatory requirements.
  • Excellent data analysis, interpretation, and problem-solving skills.
  • Demonstrated ability to work independently and as part of a team in a fast-paced setting.
  • Exceptional attention to detail and strong organizational skills.
  • Effective written and verbal communication skills.

Preferred Qualifications

  • Master's degree in Chemistry or a related field.
  • Experience with method development and validation.
  • Knowledge of statistical process control (SPC) and quality management systems.
  • Familiarity with LIMS (Laboratory Information Management System) and other electronic documentation systems.
  • Experience with sterile or aseptic manufacturing environments.

Perks & Benefits

  • Comprehensive Medical, Dental, and Vision insurance plans.
  • Paid Time Off (PTO) and company-paid holidays.
  • 401(k) retirement plan with company match.
  • Employee stock purchase program.
  • Tuition reimbursement and professional development opportunities.
  • On-site fitness center and wellness programs.
  • Employee assistance program (EAP).
  • Life and disability insurance.
  • Discounts on Abbott products and services.

How to Apply

If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:

  • An up-to-date Resume or CV
  • A brief cover letter summarizing your experience and motivation

Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.

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