Development Engineer in Medical Devices

We offer market leading technique for laser surgery, equipment for cataract operations and intraocular lenses. We also offer a program for education and support that help eye surgeons to master the full range of the technology. Johnson&Johnson Vision in Uppsala produce the ophthalmic viscoelastic device Healon. We manufacture our products from scratch. A substance is produced from raw materials and is through different steps in production processed to finished products. The whole process takes several days and monitored closely. A variety of quality assurance measures are made continuously. It is important that the product is free from particles, fibers and odor. Improvements to the product and the process are made continuously to lift the organization to a more efficient level and to position ourselves in front of our competitors. At our site in Uppsala, there are many different tasks and employees with different experiences and skills. We are about 120 employees located in Uppsala and 8 400 employees worldwide within Johnson&Johnson Vision.

Johnson & Johnson is a company committed to doing good for the world. We blend Heart, Science and Ingenuity to profoundly change the trajectory of health for humanity.
Johnson&Johnson Vision is a leading global optical company that develops life changing techniques for all ages. We provide eye surgeons and their patients with a complete solution that includes a range of advanced products and services developed to help people of all ages with sight defects.

Overall purpose of job:

This position is responsible for the design, development, verification, and validation of new products from concept through design transfer/production using the process and tools identified in the J&J AMO AB Quality System related to design controls Essential duties and responsibilities:

* Act as the technical contributor on a new product development project team.

* Primary responsibilities include; concept development, prototyping, product design, verification/validation testing including authorship of protocols and reports, and support through production scale up.

* Create and maintain design control related documentation such as risk and usability assessments, user needs, design Inputs, etc. Comply with requirements of design controls and other regulatory bodies.

* Design products in conjunction with the manufacturing engineering/external supplier groups in order to deliver a design that is manufacturable.

* Develops and validates Chemical and Mechanical test methodologies to evaluate devices both in development and currently on the market.

* Will support Marketing/Sales with competitive product analysis and performance testing

Start:Preferebly June 14th or as agreed.

Length: Initial duration of 5 months

Occupancy: 100%