Quality Control Chemist II 1st Shift

Overview

Stryker is hiring for a QC Chemist II onsite in Cary, IL
. The position involves performing advanced analytical analysis of raw materials, in-process solutions, stability, finished goods, cleaning samples, and providing general laboratory support.

• Responsible for conducting simple/complex data review.
• Performs routine and non-routine analysis for raw materials, in-process solutions, stability, and finished goods.
• Executes Phase I, Phase II, and nonconformances. Applies fundamental concepts for problem solving. Leads basic root cause investigation events.
• Understands and follows regulatory requirements in their area of work, and can explain basic concepts to extended teams.
• Responsible for simple instrument troubleshooting and vendor communication.
• Performs laboratory maintenance activities including but not limited to equipment preventative maintenance, calibration, etc.
• Independently creates or approves records containing technical writing, including/not limited to NC/CAPA investigations and procedures. Provides basic feedback to record owners when acting as approver.
• Works with continuous improvement principles within their functional area and identifies projects/opportunities (e.g., 6S).
• With guidance, leads in design/development of process/test methods.
• Applies knowledge of validation principles.
• Supports projects effectively, works within project timelines, and develops plans for projects in their area of responsibility.
• Constructs and delivers presentations in their area of responsibility that convey a clear message; comfortable presenting in various forums and able to articulate a clear message.
• Maintains a safe, clean, and organized work environment free of safety hazards.
• Demonstrates Stryker’s Leadership Expectations and shows a strong commitment to self-development.
• Performs other routine/non-routine activities as needed.

• Bachelor’s Degree in Science or Chemistry.
• 2+ years of experience working in a GxP laboratory environment and good manufacturing practice (cGMP).
• Ability to work independently with minimal supervision.

• Experience with maintenance of HPLC, UHPLC, or GC.
• Strong written and oral communication skills.
• Experience with common laboratory equipment such as balances, graduated cylinders, etc.
• Experience with common analytical methods such as chromatography and spectroscopy.
• Experience conducting compendial analytical testing.
• Experience working with Laboratory Information Management System (LIMS).
• Proficient in Microsoft Office applications.

• Salary: 76,500. USD annually, salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.

Posted:
February 4, 2026