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Associate Project Manager, Regulatory Affairs /Quality Assurance

Requisition ID 29427BR
Job Title Associate Project Manager, Regulatory Affairs /Quality Assurance
Group MedSurg and Neurotech
Division Medical
Business Function Regulatory Affairs
Country United States
State/Province IL
City Cary
Employment Category Full Time
Percent Travel Required Up to 10%
Shift 1st
About Stryker
Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. More information is available at www.stryker.com All qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status, or any other characteristic protected by applicable law. We are an EO employer ? M/F/Veteran/Disability.
Job Description / Information
The Associate Project Manager, RA/QA is responsible for leading and directing complex projects which require considerable resources and high levels of functional integration. This role will be responsible for all aspects of the project from initiation to completion. You will interface with a diverse group of stakeholders and end users.
In this role, you will:
+ Assemble a project team and assign individual responsibilities, identifying appropriate resources and developing schedules to ensure timely completion of the project.
+ Lead the identification, assessment, monitoring and closure of project risks throughout the project lifestyle.
+ Develop a project plan that analyzes the regulatory/quality pathways while evaluating the risk-benefits.
+ Serve as subject matter expert with a demonstrated knowledge of both Regulatory and Quality processes and procedures.
Minimum Qualifications
What you need
+ BS in Engineering, Science or related. MS or RAC(s) preferred.
+ A minimum seven years' experience in Regulatory Affairs and/or Quality Assurance.
+ Pharmaceutical, medical device, or cosmetic experience. Preference for pharmaceutical experience.
+ PMP certification or equivalent is desired.
All qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status.
Stryker is an EO employer ? M/F/Veteran/Disability


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