Position: Associate

Job type: Full-time

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Job content

Who we are

In a life without sound, our work provides meaning. As a leading provider of innovative hearing care solutions, we are not just a company that makes products: we are a team on a mission to help people enjoy the delight of hearing. To enable a life without limitations, we – through our core business brands Phonak, Unitron, Hansaton, Advanced Bionics and AudioNova – develop, manufacture and distribute solutions that push the limits of technology and redefine the future of our industry.

For the global process of devices risk management, the position is responsible for defining, implementing and improving the Sonova Global Quality System and Governance.

You work closely with hardware and software engineers, product managers, human factors engineers, clinical experts, vigilance experts, technical service personnel, complaint managers, and production staff to ensure the safety of the products, while supporting communications with health authorities and notified bodies as required.

Your tasks

  • Providing expertise and guidance to the organization in interpreting government regulations, agency guidelines, and internal policies to assure compliance as well as support for implementation of local and corporate Quality System requirements
  • Collaborate with Subject Matter Experts to develop clear objectives for education packages that improve competency, and are designed with high quality for comprehension and retention
  • You establish and maintain Quality Project/Program toolsets to drive efficient and effective project execution including methodologies in project and data management
  • You develop communication tools (i.e. process maps, training, documentation etc.) to ensure clear and consistent understanding of project expectations and data/metrics process across all levels of the organization

Your profile

  • Bachelor’s degree or preferably Master in engineering, natural science or quality with 8+ years of relevant work experience in a GMP environment, ideally in a medical device company
  • Previous proven quality experience on large scale enterprises in Life Science industry with significant exposure to requirements of GMP, GDP, ISO 13485, CFR 820
  • Ability to effectively manage multiple projects and priorities
  • Excellent communication and presentation skills
  • Self-driven personality with high analytical and conceptual thinking and excellent interpersonal skills
  • Fluent English skills, any other languages are an asset

Our offer

We can offer you a new challenge, with interesting tasks and much more - including an open corporate culture, flat hierarchies, support for further training and development, opportunities to take on responsibility, an excellent range of foods, sports and cultural facilities, attractive employment conditions, and flexible working time models in various roles.

Daryl Alther, Talent Acquisition Manager, is looking forward to receiving your complete application (CV, references and certificates) via our online job application platform.

For this vacancy only direct applications will be considered.

Sonova AG

Laubisrütistrasse 28

CH-8712 Stäfa

Sonova is an equal opportunity employer.

We team up. We grow talent. We collaborate with people of diverse backgrounds to win with the best team in the market place. We guarantee every person equal treatment in regard to employment and opportunity for employment, regardless of a candidate’s ethnic or national origin, religion, sexual orientation or marital status, gender, genetic identity, age, disability or any other legally protected status.

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Deadline: 08-04-2024

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