Quality & Regulatory Affairs Associate (CL718091)

Requisition Number

EMEA09560

Employment Type

Full-time

Location

Riyadh

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.
Learn more about us by visiting zimmerbiomet.com

What You Can Expect

The Quality and Regulatory Affairs Associate is responsible of the product
registration in
different markets in accordance with the local legal requirements. Also the
main
contact between the organization and authorities to ensure reliable forward of
information.

How You Create Impact

• Support implementation, development, maintenance and control of a quality
  management system according to international standards and corporate
  guidelines/policies/procedures


• Manage customer complaints handling and instructed actions e.g. product blockings, recalls, provide field safety notices, etc. Product enquiries on own responsibility via SAP system are essential required


• Responsibility for product registration on the market in accordance with local legal requirements; main contact for the local competent authority and responsibility for the maintenance of the business in the local market


• Assure an effective, consistent and reliable forward of information in terms of product surveillance on the local market in accordance with legal requirements and Zimmer procedures


• Surveillance and forward of information concerning changes and/or new upcoming local legal requirements to assure the continuity of Zimmer's business


• Support the internal and external audits; also within an internal auditor team coordinated by headquarters (if applicable)


• Continuous communication with QA/RA EMEA


• Support other Zimmer distribution organizations with regards to QA/RA requirements(e.g. product registrations)


• Involvement in special projects and special duties like (re-)validation of technical
  systems and procedures

What Will Make You Stand Out

• Microsoft Excel


• SAP


• Knowledge of ISO ‎9001, ISO ‎13485 and Medical Device Directive is a plus


• Knowledge of national medical device regulations


• Fluency in English, spoken & written.


• French is a plus


• Solid problem solving skills


• Ability to work independently and under pressure


• Organizational, follow up and time management skills

What Will Make You Successful

• Bachelor's Degree in Engineering, Business or Political Science.


• ‎1 to ‎2 years of experience in registration activities and/or quality assurance with
  preference to international medical device regulations.

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