Quality Control Chemist II (Thursday - Monday, 1st Shift)

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

What you will do:

• 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, 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. 
• Working knowledge of continuous improvement principles within functional area with ability to identify projects/opportunities (e.g 6S). 
• With guidance, lead in design/development of process/test methods. 
• Working knowledge and ability to apply validation principles. 
• Supports projects effectively, works within project timelines, develops plans for projects in area of responsibility. 
• Constructs and deliver presentations in area of responsibility that convey a clear message, comfortable occasionally presenting in various forums, ability 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. 

What you need

• Bachelor’s Degree in Science or Chemistry.
• 2+ years' experience working in a GxP laboratory environment and Good Manufacturing Practice (cGMP).
•  Ability to work independently with minimal supervision.

​​Preferred:

• Experience with maintenance of HPLC (High Pressure Liquid Chromatography), UHPLC (Ultra High Pressure Liquid Chromatography) or GC (Gas Chromatography).
• 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, spectroscopy, etc.
• Experience conducting compendial analytical testing.
• Experience working with Laboratory Information Management System (LIMS).
• Proficient in Microsoft Office applications.

• 76,500.00 - 122,000.00 USD Annual salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.

Posted: February 4, 2026