Temp Ra Systems Associate

vor 1 Woche

Zug, Schweiz Zimmer Biomet Vollzeit

-Requisition Number
EMEA10596
Employment Type
Full-time
Location
Zug

**What Is It Like To Work at Zimmer Biomet**:
At **Zimmer Biomet**, we believe in **The Power of Us**, which means that we are stronger together. We are committed to creating an environment where every team member feels included, respected, empowered, and celebrated.

**Zimmer Biomet Offers You An Exciting Position With Good Career Prospects in a Fast-growing International Business, And a Competitive Remuneration Package**
- Possibility to grow, develop, and be promoted within a Team
- Friendly, warm and creative atmosphere
- Healthy, inspiring, and international work environment
- Ongoing coaching and talent development
- Access to future career opportunities
- Hybrid work model
- Competitive reward packages
- Annual bonus
- Social and CSR events
- Wellbeing initiatives

**What You Can Expect**:
The Regulatory Affairs data analyst supports the Corporate Regulatory Affairs team in EMEA with primary focus on distribution control in the region. The resource will help reviewing existing processes and identifying improvements or needs for new ones; will provide trainings to the Regulatory Affairs team members in the region and additional support to APAC and Americas as needed.

**How You Create Impact**:

- Collect and review Objective Evidence for Regulatory Affairs systems (e.g. RIMS, GTS)
- Update RA Systems as needed (e.g. RIMS/GTS/Batch Determination/Sales Block) and support tests (either from IT and the business)
- Generate reports on distribution control activities as needed
- Support procedures and processes review and provide trainings as needed
- Verify the integrity and accuracy of information against source documents and make corrections and adjustments when necessary.
- Work with in-country resources to collect and verify objective evidence as needed
- Coordination and communication with Business Units Regulatory Affairs or Global Customer Operations as needed

**What Will Make You Stand Out**:

- A Bachelor's Degree in life science or other quantitative fields
- English: Proficiency spoken and written
- German and/or Dutch would be an asset
- Other EU languages are a plus

**What Will Make You Successful**:

- 1-3 year of experience in the medical device, pharmaceutical or biotech industries
- Experience working with Microsoft software (e.g. Excel, SharePoint)
- Experience working with SAP strongly preferred
- Experience with Regulatory Information Management Systems preferred
- Strong sense of urgency and attention to detail
- Good communication and organizational skills with the capacity to prioritize and multi-task
- Understanding of the regulatory environments, FDA and other federal regulations, and ethical guidelines
- Ability to develop good working relationships with colleagues across the entire organization and with different backgrounds

**Who We Are**:
**Zimmer Biomet** is a world leader in musculoskeletal health solutions. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to _alleviating pain and improving the quality of life for people around the world_.
- Looking to make an impact? Join us and make a difference._

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