SUMMARY
The successful candidate will have product development experience and
will be capable of delivering innovative new products and successfully
participating in cross-functional Technology or New Product
Development teams for global continence care related projects.
The successful candidate will be capable of interfacing with
colleagues at all levels within the organization and will effectively
deliver product solutions which benefit our customers.
RESPONSIBILTIES
The successful candidate will be responsible for:
* Representing the product development function in cross-functional
product commercialisation teams from Front End Innovation through to
Commercial Launch.
* Design and development of new products, including concept
development, high-level design feasibility, prototype development,
detailed design, test method development, design
verification/validation, shelf-life determination and product
commercialisation.
* Application of both new and existing technologies, materials and
processes to deliver the optimum product design ensuring the
establishment of excellent standards of performance.
* Liaising with clinicians and with customers to understand their
needs and to therefore optimize product functionality and performance.
* Preparation of technical documentation in accordance with
regulatory and design control requirements and with the
company&#**Apply on the website**;s development processes.
* Developing a high level of understanding of internal customer
requirements.
* Conducting sophisticated analysis of data and developing detailed
reports documenting results, conclusions and recommendations
QUALIFICATIONS
ACADEMIC/CREDENTIALS/CERTIFICATIONS
* An honours Bachelor?s Degree in engineering or related
discipline is required.
* A post graduate qualification in a related discipline is
preferred.
* Project Management experience is preferred.
LENGTH OF EXPERIENCE
* **Apply on the website** years product development in medical
device design is required.
SPECIALIZED SKILLS/TECHNICAL KNOWLEDGE
* Experience in medical device design principals, material
selection, design concept validation and test method development is
required.
* Experience of working under medical device design controls, with
proven knowledge of design verification/validation and design/process
FMEAs is required.
* Demonstrated understanding of various types of manufacturing,
mechanisms, materials, tolerance-analysis and design-for-manufacturing
is required.
* Experience of medical device regulations including GMP (Good
Manufacturing Practices), QSR (Quality Systems Regulations) and ISO
quality requirements is preferred.
* Strong initiative and follow through in executing project
responsibilities, overcoming obstacles and balancing multiple
priorities effectively through strong technical and/or project
leadership experience is required.
* A demonstrated track-record of being part of successful
cross-functional product development teams is required.
* Excellent problem solving, decision making and root cause analysis
skills are required.
* The ability to effectively communicate concepts, ideas and
knowledge to all levels of the organisation is required.
* Proficiency with MS Office suite is required.
* Proficiency with CAD software is preferred.
FOR FURTHER INFORMATION ON THIS R&D ENGINEER ROLE IN MAYO PLEASE
CONTACT AMANDA REYNOLDS ON **APPLY ON THE WEBSITE**/
CHECK OUT ALL OUR OPEN JOBS ON OUR HERO RECRUITMENT WEBSITE ?
https:///
Please Note: Under its obligation under the Data Protection
legislation, HERO Recruitment will not forward your details to any
company without your prior approval.
JOB-**Apply on the website**R&D ENGINEER
SUMMARY
The successful candidate will have product development experience and
will be capable of delivering innovative new products and successfully
participating in cross-functional Technology or New Product
Development teams for global continence care related projects.
The successful candidate will be capable of interfacing with
colleagues at all levels within the organization and will effectively
deliver product solutions which benefit our customers.
RESPONSIBILTIES
The successful candidate will be responsible for:
* Representing the product development function in cross-functional
product commercialisation teams from Front End Innovation through to
Commercial Launch.
* Design and development of new products, including concept
development, high-level design feasibility, prototype development,
detailed design, test method development, design
verification/validation, shelf-life determination and product
commercialisation.
* Application of both new and existing technologies, materials and
processes to deliver the optimum product design ensuring the
establishment of excellent standards of performance.
* Liaising with clinicians and with customers to understand their
needs and to therefore optimize product functionality and performance.
* Preparation of technical documentation in accordance with
regulatory and design control requirements and with the
company&#**Apply on the website**;s development processes.
* Developing a high level of understanding of internal customer
requirements.
* Conducting sophisticated analysis of data and developing detailed
reports documenting results, conclusions and recommendations
QUALIFICATIONS
ACADEMIC/CREDENTIALS/CERTIFICATIONS
* An honours Bachelor?s Degree in engineering or related
discipline is required.
* A post graduate qualification in a related discipline is
preferred.
* Project Management experience is preferred.
LENGTH OF EXPERIENCE
* **Apply on the website** years product development in medical
device design is required.
SPECIALIZED SKILLS/TECHNICAL KNOWLEDGE
* Experience in medical device design principals, material
selection, design concept validation and test method development is
required.
* Experience of working under medical device design controls, with
proven knowledge of design verification/validation and design/process
FMEAs is required.
* Demonstrated understanding of various types of manufacturing,
mechanisms, materials, tolerance-analysis and design-for-manufacturing
is required.
* Experience of medical device regulations including GMP (Good
Manufacturing Practices), QSR (Quality Systems Regulations) and ISO
quality requirements is preferred.
* Strong initiative and follow through in executing project
responsibilities, overcoming obstacles and balancing multiple
priorities effectively through strong technical and/or project
leadership experience is required.
* A demonstrated track-record of being part of successful
cross-functional product development teams is required.
* Excellent problem solving, decision making and root cause analysis
skills are required.
* The ability to effectively communicate concepts, ideas and
knowledge to all levels of the organisation is required.
* Proficiency with MS Office suite is required.
* Proficiency with CAD software is preferred.
FOR FURTHER INFORMATION ON THIS R&D ENGINEER ROLE IN MAYO PLEASE
CONTACT AMANDA REYNOLDS ON **APPLY ON THE WEBSITE**/
CHECK OUT ALL OUR OPEN JOBS ON OUR HERO RECRUITMENT WEBSITE ?
https:///
Please Note: Under its obligation under the Data Protection
legislation, HERO Recruitment will not forward your details to any
company without your prior approval.
JOB-**Apply on the website**
We need : English (Good)
Type: Permanent
Payment:
Category: Others
