Protein Design Scientist

Syngenta Group•Durham, NC

1d•Onsite

About The Position

Perform QC laboratory chemical analysis to support production. This includes analysis of raw materials, process intermediates, agricultural formulations, and environmental samples. The Quality Control Chemist will also analyze samples for residual impurities and perform instrument maintenance on analytical instrumentation in the lab. In addition to routine Quality Control analysis and instrument maintenance, the QC Chemist will take on backup responsibilities to the Senior Quality Control Chemist to maintain a robust support structure for the Omaha QC team.

Requirements

Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Chemical Engineering, or another scientific discipline.
Experience operating and troubleshooting analytical instrumentation including HPLC, UPLC, GC, and related laboratory equipment.
Strong understanding of quality control principles, laboratory procedures, SOPs, and QA/QC requirements.
Demonstrated technical problem-solving and analytical skills with the ability to interpret complex data.
Proficiency with Microsoft Office applications, including Excel, Word, Outlook, and PowerPoint.
Excellent organizational skills, attention to detail, and ability to manage multiple priorities in a fast-paced environment.
Strong verbal and written communication skills with the ability to collaborate across departments and functions.

Nice To Haves

Master's degree in Chemistry, Analytical Chemistry, or a related scientific field.
Experience with LC/MS, FT-NIR, Laboratory Information Management Systems (LIMS), and Chromatography Data Systems (CDS).
Experience leading analytical method development, validation, or troubleshooting projects.
Knowledge of residual impurity analysis and regulatory testing requirements within a manufacturing or chemical production environment.
Experience supporting environmental testing, product registration activities, or customer complaint investigations.
Continuous improvement mindset with experience participating in process optimization or operational excellence initiatives.
Demonstrated ability to influence change, drive improvements, and work effectively within cross-functional teams.

Responsibilities

Champion a strong safety culture by adhering to all Syngenta safety policies, regulatory requirements, and operational procedures.
Lead the residual impurity (RI) analysis program, including method development, troubleshooting, validation, and reporting in partnership with the QC Manager.
Conduct and interpret analytical testing of raw materials, intermediates, finished products, environmental samples, and rinsates using HPLC, UPLC, GC, LC/MS, FT-NIR, and wet chemistry techniques.
Ensure all analytical data is accurate, timely, defensible, and generated in compliance with established SOPs, QA/QC standards, and regulatory requirements.
Investigate analytical issues, troubleshoot laboratory instrumentation and methods, and perform routine maintenance on laboratory equipment to ensure reliable performance.
Support continuous improvement initiatives, incident investigations, customer complaint analysis, and process optimization efforts across the Quality Control laboratory and manufacturing operations.
Collaborate cross-functionally with Operations, PT&E, and Quality teams to improve processes, develop SOPs, support product registrations, and maintain laboratory data management systems.