Position: Mid-Senior level

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.

We are looking for a Quality Assurance Manager for our Phonak Marketing team. You will be one of the main points of contact for QMS in Phonak Marketing and will closely collaborate with Quality Managers from other departments to ensure regulatory compliance of the QMS setup and support the Marketing organisation in optimising the process landscape.

Your tasks

  • Run the daily business activities and ensure compliance of marketing processes to regulatory requirements
  • Support the process/procedure owners in implementation and maintenance of regulatory requirements in marketing QMS relevant documentation
  • Support the teams in the maintenance and handling of the eQMS
  • Supports the training of the processes & SOP’s to the involved parties
  • Support the Process Owner in definition and measurement KPI’s and annual Targets
  • Supports the continued improvement of the QMS documents within the process in a timely manner
  • Support organisation in preparation of and during audits and resolution of non-conformities if received during an audit
  • Support the product development teams regarding implementation of internal product design procedures, completion of the technical documentation deliverables
  • Support of the QMS globalisation across legal entities of Sonova AG

Your profile

  • 2-3 years of experience as Quality Manager in a medical device regulatory environment
  • BSc degree in Business Administration, Engineering, Life Science or relevant field is a plus
  • In-depth understanding of quality control procedures and relevant legal standards, experience in the medical device design control process is appreciated
  • Detail-oriented, diligent, and responsible person
  • Pragmatic and result-oriented problem-solving approach
  • Ability to liaise within a cross-functional and intercultural team
  • Excellent Microsoft Office skills, SAP is a plus
  • Excellent English skills (oral and written), German is a plus

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.

Kira Maurer, Talent Acquisition Manager, is looking forward to receiving your complete application (cover letter, 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

+41 58 928 01 01

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: 10-05-2024

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