Achieva Group Ltd

Device Design Engineer

5 days left

£45000 - £55000 per annum
20 May 2021
19 Jun 2021
Perry Moore
Full Time
Contract Type
Experience Level
Experienced (non-manager)

Our client, a leader in the field or Device Design and Development, are seeking an experienced Design Engineer to join their team on a permanent basis.
As a Device Design Engineer, you will be joining an established and experienced design team and you will be responsible for designing and developing drug delivery systems.
The ideal candidate will be mechanically trained, and additional experience of Finite Element Analysis (FEA) would be an advantage.

Role Responsibilities
Responsible for applying knowledge of materials, manufacturing processes, finishing and assembly to develop cost-effective and robust devices.
Writing technical reports and producing high quality design documentation within a regulatory controlled GMP environment.
Responsible for submitting your designs with solid engineering principles, you will carry out in-depth calculations and tolerance analysis to evaluate technical risks to ensure the design is robust.
Liaising with external partners/suppliers and others to support industrialisation, scale-up and verification of device design and to ensure an integrated approach to overall project delivery.

Experience and Background
Fluent with 3D CAD; Creo and/or Solidworks.
Experience of Finite Element Analysis (FEA) desirable.
A 1st or Upper 2nd class degree from a respected university in mechanical engineering or a related discipline.
Must possess mechanical creativity, insight and attention to detail applied to the creation of reliable mass-produced devices.
Track record of having produced high-quality design in advanced mechanical product development projects.
Experience and knowledge of manufacturing and assembly processes and the key drivers for high volume manufacture, with experience (ideally) in plastic injection moulding.
Awareness of the principles of Design Control, as these will underpin your work within our quality management system, accredited to ISO 13485 & FDA 21 CFR Part 820.

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