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Software Senior Engineer M/w
Il y a 4 mois
**Requisition Number**: EMEA10568
**Employment Type**: Full-time
**Location**: Montpellier
**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**:
As a Software Engineer within our R&D team, you will:
- Contribute to the definition and monitoring of product system requirements, for devices under development as well as for products already on the market.
- Analyze the various possible technical choices, propose them to the team and participate in the selection of the best solution
- Participate in device risk management activities (FMEA, patient risks, cybersecurity)
- Check links between software requirements and subsystems and vice versa, in collaboration with the system team or other subsystems.
- Guarantee the conformity of the deliverables you produce
- Participate in integration and verification activities (strategy, protocols, execution, reporting)
- Participate in usability activities (strategy, protocols, execution, reports)
- Provide technical support for design transfer activities
- Contribute to the creation, update and management of technical documents
- Contribute to impact analyses in case of design change on a device already on the market
- Support the certification team during evaluation tests and to establish the required files
- Support the QARA team (Quality and Regulatory) in drawing up regulatory files (CE, FDA, etc.)
- Support the Post Market Surveillance team in investigations and problem solving
- Contribute to the improvement of working methods
**What Will Make You Stand Out**:
You have an engineering degree or equivalent, and at least 8 years' relevant professional experience.
As a Software Engineer, you will be involved in a variety of projects, consisting of a system and several subsystems (e.g.: Hardware, Software and Robotics); you will mainly be involved in the software subsystem, but must have a general understanding of the complete system.
Ideally, you have a previous experience in complex medical devices.
**What Will Make You Successful**:
**Required skills**
- Knowledge of C++ programming
- Proficiency in the use of the Visual C++ or similar development environment
- Knowledge of the regulatory environment (ISO 13485, IEC 62304, FDA)
- Ability to analyze, summarize and solve problems
- Good interpersonal skills
- Rigor and autonomy
- Proactivity and ability to make proposals
- Fluent English
**Desirable Skills**
- Knowledge of operating room constraints
- Knowledge of ISO 13485 and ISO 14971
- Knowledge of IEC 60601 and 62304
**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._
