True to the vision "We drive innovation to improve people's lives", the Hamilton companies have been providing solutions for the health sector since 1950. We are an innovative pioneer in the fields of ventilators, automated pipetting, sample management and in the development of process sensors.Hamilton Medical is a leading manufacturer of intelligent ventilators. Whether in ICUs, during emergency rescue transport or an MRI scan - our solutions cover a multitude of patient groups, applications and environments.
How you can make a difference:
Support R&D with material selection for critical components in relation to ISO 18562-1-4, ISO 10993-1-23 and in conformity with global legislations related to material compliance
Support the implementation of material compliance data management
Contribute to supplier quality by providing input to quality management agreements in relation to material compliance and biocompatibility
Support material changes and set up internal processes for managing changes efficiently
Support and document V&V activities in materials testing related to chemical and biological safety for product lifecycle management, change management and new product development
Assisting with any potential product field re-engineering, corrective action, related to material compliance topics, including necessary support to regulatory agencies and customers
Collaborate with Suppliers and internal Stakeholders to drive Quality improvements that minimize the Costs of Quality and support implementation of Supplier/Engineering changes, New Product Introductions and Transfers
That's what you bring along:
Degree in an engineering discipline or equivalent non-technical degree with experience in chemical or materials manufacturing, engineering or quality assurance
You are familiar with: materials regulatory framework in EU, US and ROW, including but not limited to: MDR 2017/745, REACH, ROHS, POP, California Proposition, Conflict minerals, TPCH
Qualified verification and validation engineer, who can lead, acknowledge, develop, communicate & implement materials testing strategies to ensure compliance to Medical Device requirements
Effective problem solver, with the skills to lead Root Cause investigations plan complex workstreams and influence others cross-functionally
Ideally, you gained first-hand experiences in dealing with complex regulations and compliance requirements for legal entities and products designed, developed, manufactured, distributed and sold by those entities in ideally global markets
Able to use English and German as working language, excellent communicator and collaborator who can influence at all levels of the organization
You have experience with: ISO 10993-series, preferably also with ISO 18562-series of standards
Learn more about career opportunities at Hamilton at jobs.hamilton.ch.
Do you share our values and feel at home in a cooperative and down-to-earth environment? At Hamilton, we not only offer a motivating working environment, but also various leisure activities and modern working conditions. Our interactions at eye level encourage open communication and a pleasant working environment. Become part of a team where your skills are valued and innovative ideas are fostered. Interested? Then apply online using the "Apply now" button.If you have any questions, please contact us at jobs@hamilton.ch with the following details:
Reference: JR-3963-fjm/Contact: Ilaria Cerullo
Applications by post or e-mail can unfortunately not be considered.