Quality and Regulatory Affairs Supervisor - Riyadh, المملكة العربية السعودية - Zimmer Biomet
وصف
Requisition Number:
EMEA10534
Employment Type:
Full-time
Location:
Riyadh
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 Quality and Regulatory Affairs Supervisor is responsible of the product registration in different markets in accordance with the local legal requirements.
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:
Bachelor's Degree or Master's Degree in Pharmacy, Business, Engineering
Fluency in English and Arabic, both spoken & written.
French is a plus
What Will Make You Successful:
5 to 10 years of experience in registration activities and/or quality assurance with preference to international medical device regulations.
Microsoft ExcelSAP
Knowledge of ISO 9001, ISO 13485 and Medical Device Directive is a plus
Knowledge of national medical device regulations
Solid problem solving skills
Ability to work independently and under pressure
Organizational, followup and time management skills
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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