Job Description:
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The role of Research and Development Engineer II is a challenging opportunity to contribute to the development of innovative medical products. As part of our global team, you will work on creating trusted solutions that improve patient outcomes and reduce care costs.
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We are seeking a skilled engineer with expertise in product design, materials, and processes. You will be responsible for developing new or improving existing products, systems, and process components. This includes designing and testing prototypes, preparing process specifications, and ensuring compliance with international standards and company procedures.
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Your key responsibilities will include:
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* Designing and developing new or improved products, systems, and process components.
* Developing process specifications for new products and improved processes/products.
* Preparing prototyping lines and prototypes of products.
* Performing laboratory tests at site in cooperation with Quality Management.
* Ensuring that design documentation is prepared according to required standards and established company procedures.
* Communicating effectively with Global T&I, Global Marketing, Global Quality, Regulatory and Clinical teams.
* Participating in Risk Assessments.
* Updating/create drawings in cooperation with Global R&D Engineering.
* Creating specifications of products, raw materials, semi-finished goods etc.
* Developing test methods.
* Performing Design review of drawings/measurement/test methods etc.
* Initiating and performing shelf-life testing.
* Initiating and performing biocompatibility testing (external contracting).
* Determining effects of (re)-sterilization.
* Ensuring compliance with legislative and internal requirements of EHS and participating in fulfillment of company's targets in EHS area.
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For Existing Product Remediation Purpose:
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You will be responsible for developing product design Inputs/Outputs, performing Product design verification, performing Product design validation, performing Final Design Review, and any other duties assigned by the immediate superior.
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Authority:
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You will have the authority to approve R&D Approver / technical Approver and R&D Owner Change Control Record (CCR’s and ECCF’s).
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Required Skills and Qualifications:
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To be successful in this role, you should have good analytical skills and technical knowledge in product development and design, materials, and processes. You should also be proficient in computer systems such as Microsoft Office, Microsoft Excel, Minitab (or equivalent), and Solidworks (AutoCAD). Effective communication skills in English are essential, as well as the ability to work independently and as part of a team.
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Benefits:
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This role offers a range of benefits, including flexible working hours, home office possibilities, and opportunities for professional growth and development. You will also have access to ongoing training and support to help you succeed in your role.
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Others:
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Please note that travel requirements may involve up to 25% of time, mostly within Europe but overseas travel is expected (variable and project-related). Most trips will include overnight travel.