Quality Associate II
Round Lake, IL
Req ID 51250BR
Business Title
Quality Associate II
Business
Global Quality
Sub-Business
Medical Products Support
Country
US
State/Province
Illinois
Location of Position
Round Lake, IL
Shift_
1st
Job Description
•Support the activities of the Franchise process improvement function to enhance the overall quality systems resulting in increase efficiency, improve effectiveness, resolved operational issues and cost savings. •Conduct trend analysis across quality systems (Customer Complaints, CAPA etc) on a routine basis to identify opportunities •Lead/support improvement projects.
•Assure project goal clarity and focus •Develop project plans •Secure project support and membership •Motivate team to meet milestones and project due date •Identify and communicate barriers/obstacles to project sponsors •Present project outcome to sponsors and propose project closure
•Support the Franchise quality system and product/process performance data streams to assure accurate and timely communication of key quality indicators to quality and business stakeholders. Create Quality System and Product Quality power point presentations for Senior Staff review •Write, revise and review SOP's •Perform third party batch record review and product release activities.
Job Requirements
Education and/or Experience.
Bachelor's degree in the sciences or in engineering, 3-5 years experience in Quality Assurance or QC/QA analysis. Experience in working with third party contract manufactures. Experience in Manufacturing Operations is highly preferred.
•Strong organizational, problem solving, and time management skills. Ability to lead/support multiple projects concurrently and drive to completion.
•Excellent presentation skills and confident in public speaking. Ability to compose power point presentation.
•Familiar with operating procedures, quality and regulatory requirements pertinent to pharmaceutical, biological, and medical devices.
•Must be able to apply sound scientific principles and compliance standards to quality projects.
•Must have excellent interpersonal skills; and be able to effectively communicate and influence project members.
•Familiar with product/process change control and nonconformance investigations.
•Ability to write and review effective technical documents as it relates to change controls and investigations.
•Computer Efficient (ISO Train, Trackwise, BPLM, Microsoft Office, etc.)
Doing Work that Matters
Baxter provides its employees with comprehensive compensation and benefits. To view additional opportunities at Baxter and to learn more about the company, please visit our Web site at company website. EOE M/F/D/V.
