**Why engineering at Stryker?
****:
At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products.
As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better.
Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products.
You will also have growth opportunities as we have a culture that supports your personal and professional development.
**Who we want**
- ** Detail-oriented process improvers.
** Critical thinkers who naturally see opportunities to develop and optimize work processes - finding ways to simplify, standardize and automate.
- **Data translators.
** Highly effective communicators who can transform data findings into recommendations to compose reports and executive level presentations.
- **Meticulous documenters.
** Detail-oriented people who enjoy maintaining meticulous documentation of reports, metrics, proposals, and presentations.
- ** Self-directed imitators.
** People who take ownership of their work and need no prompting to drive productivity, change, and outcomes.
- ** Strategic thinkers.
** People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.
**What will you do**
Collaborates with suppliers to assure the quality of their products, materials, components and/or operations.
Monitors supplier performance and supports efforts to develop and implement changes to improve the production process.
Follows up with suppliers on quality deviations and ensures that solutions are identified and implemented.
Responsible for quality related activities as it applies to Product Transfer, these include but not limited to the following:
- Supporting all transfers globally, (Supplier to Supplier, Supplier to Stryker, Stryker to Supplier, Stryker to Stryker)
- Having knowledge of and ability to provide interpretation and perform on Regulations, Corporate and Site Local procedures as they relate to quality activities such as DFMEA, MSA's, Validations and Qualifications.
- Executing, reviewing and approving of Validation/Qualification Documentation.
- Enable successful completion of product transfer to achieve its quality, cost and time requirements
**What will you need**
- Bachelor's degree in engineering or related fields
- 2 to 3 years of experience in similar positions- Intermediate English- Microsoft Office knowledge- Medical Industry Regulations background
**Know someone at Stryker?
**:
**About Stryker**:
Stryker is one of the world's leading medical technology companies and, together with our 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.