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

Stryker•Cary, IL

1d•$76,500 - $122,000•Onsite

About The Position

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. Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces!

Requirements

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

Nice To Haves

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 (English).
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.

Responsibilities

Performs routine and non-routine analysis for raw materials, in-process solutions, stability, and finished goods.
Responsible for conducting simple/complex data review.
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.