Benefits Package:
£35,000 - £40,000 Genuine progression opportunities available Extremely stable company Further benefits
Company Overview: A world-class medical device supplier with a very lucrative product range is rapidly expanding the organisation. Due to significant investment, the company has acquired new businesses and is growing its brand worldwide. The product range is established throughout the UK, Asia, America, Mexico, Europe, and more, with plans to branch out further next year. This makes it a great time to join this lucrative organisation.
Role & Responsibilities:
Product design and development of medical devices from concept to market release. Compiles DHF (product design, specifications, DFMEA, design testing, verification, validation, usability). Leads project actions in the UK and Manufacturer (design transfer). Provides engineering requirements for ECOs. Maintains allocated legacy DHFs. Verification and validation of components and assemblies (ISIR and appropriate testing, as required). Records all formal and relevant informal engineering information in the PLM system. Modification/amendment of new/existing drawings in accordance with design standards. Other reasonable duties which may be requested by your manager.
Knowledge, Skills & Experience: Problem-solving techniques (i.e. DFMEA/Risk Analysis). Experience in compilation of usability engineering file. Experience working as a Design Engineer within a manufacturing environment. Design requirements of extruded/moulded parts. Understanding of ISO13485:2003/MED DEV 93/42/EEC and/or FDA regulations. Experience of working with a Product Life-Cycle Management System and/or working with an ERP System is highly desirable. Bill of Materials Creation and Management.
If you are interested in this position, please click 'apply'.
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£35,000 - £40,000 Genuine progression opportunities available Extremely stable company Further benefits
Company Overview: A world-class medical device supplier with a very lucrative product range is rapidly expanding the organisation. Due to significant investment, the company has acquired new businesses and is growing its brand worldwide. The product range is established throughout the UK, Asia, America, Mexico, Europe, and more, with plans to branch out further next year. This makes it a great time to join this lucrative organisation.
Role & Responsibilities:
Product design and development of medical devices from concept to market release. Compiles DHF (product design, specifications, DFMEA, design testing, verification, validation, usability). Leads project actions in the UK and Manufacturer (design transfer). Provides engineering requirements for ECOs. Maintains allocated legacy DHFs. Verification and validation of components and assemblies (ISIR and appropriate testing, as required). Records all formal and relevant informal engineering information in the PLM system. Modification/amendment of new/existing drawings in accordance with design standards. Other reasonable duties which may be requested by your manager.
Knowledge, Skills & Experience: Problem-solving techniques (i.e. DFMEA/Risk Analysis). Experience in compilation of usability engineering file. Experience working as a Design Engineer within a manufacturing environment. Design requirements of extruded/moulded parts. Understanding of ISO13485:2003/MED DEV 93/42/EEC and/or FDA regulations. Experience of working with a Product Life-Cycle Management System and/or working with an ERP System is highly desirable. Bill of Materials Creation and Management.
If you are interested in this position, please click 'apply'.
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