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Stryker.

Associate Project Manager, Regulatory Affairs /Quality Assurance

Stryker. - Cary, IL

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

Who we want

Strategic. Creates alternative ways to proceed. Faced with any given scenario, can quickly spot the relevant patterns and issues.

Achiever. Strong work ethic with a “leads by example” mindset.

Deliberative. Good judgement with ability to identify risks and make sound decisions.

Learner. Demonstrated commitment to learning and the ability to transfer knowledge, ideas and concepts.

Collaborate. Builds and maintains relationships cross functionally as well as externally to create opportunities.

Communicator. Articulates well and expresses ideas effectively.

What you will do

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 be responsible, but not limited to the following:

Assembling a project team and assigning 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.

Developing 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 of 7 years’ experience

in Regulatory Affairs and/or Quality Assurance.

Must have pharmaceutical, medical device, or cosmetic experience. Preference for pharmaceutical experience.

PMP certification or equivalent is desired.

12 days 4 hours ago

Stryker.

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Associate Project Manager, Regulatory Affairs /Quality Assurance Stryker. - Cary, IL, United States

   

Location: Cary, IL

Company Profile:
Stryker is one of the world's leading medical technology companies and, together with our customers, we are driven to make healthcare better. The Company offers a diverse array of innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. Stryker is active in over 100 countries around the world.