- Full Time
- Temporary
Related content
Why join Stryker?
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine!We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
12 month fixed term contract, on site position in Anngrove, Cork
Position Summary
This role performs professional engineering work in the conception, specification, design, manufacture and testing of medical device packaging. Work with design teams & suppliers by managing the process and the development of new packaging solutions. This would be, create packaging solutions for changes including conceptual design, process development, process deployment, process validation, continuous improvement initiatives, continuing production support and supplier development as well as the packaging, shipping and transportation testing required for both sterile and non-sterile packages. Help lead in the development of Standard Operating Procedures which govern the
development of product packaging.
What you will do:
- Development and management of Packaging Procedures; develop design rules and guidelines considering performance, cost, and reliability
- Develop advanced packaging designs from concept to final release including CAD documentation
- Create and maintain component specifications for all primary, secondary and tertiary packaging and develop, conduct and analyze the testing of this packaging
- Interfacing with internal product sustaining engineering team to define package design solution; Manage multiple projects to meet established timelines
- Develop an understanding of Stryker package manufacturing processes Identify viable primary packaging options and alternatives, defining technical parameters
- Development of secondary shipment packaging
- Represent JR in corporate initiatives to develop standards for packaging verification and Validation, as well as other topics related to packaging and labelling
- Write or contribute to risk management document relative to package, in coordination with the project team
What you will you need:
- 1 - 3 years of hands-on experience in Medical Device packaging design and development
- BS/BA or equivalent, in a technical field such as Packaging Engineering; Mechanical Engineering, or Materials Engineering
- Detail oriented with excellent communication and project management skills Demonstrated knowledge of QSR and medical device packaging systems, medical device industry experience is strongly preferred.
#ij