Project Development Engineer (m/f/d) Medical Device Solutions

at  Trelleborg Sealing Solutions Healthcare and Medical

70565 Stuttgart, Baden-Württemberg, Germany -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate10 Nov, 2024Not Specified11 Aug, 2024N/AItNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

Trelleborg is a world leader in engineered polymer solutions for almost every industry on the planet. And we are where we are because our talents brought us here. By specializing in the polymer engineering that makes innovation and application possible, Trelleborg works closely with leading industry brands to accelerate their performance, drive their business forward—and along the way, shape the industry and progress that will benefit humankind in the exciting years ahead. Our people are Shaping Industry from the Inside. Why don´t you join us?
We are looking for you as a Project Development Engineer (m/f/d) to initiate, secure, and implement customer projects for Trelleborg Medical Solutions. We are an end-to-end development partner for our customers from concept to full device production. You will have the opportunity to work on exceptionally exciting projects and support our customers in the medical and (bio-) pharmaceutical industry. You can be located in Switzerland, France, Sweden, Germany or the UK.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities:

  • Develop customer-specific solutions for medical products in an interdisciplinary project team, from the creation of a specification sheet to series production.
  • Provide support in the preparation and follow-up of quotations and processing of orders within the customer team.
  • Lead project management by coordinating interdisciplinary project teams (manufacturing, quality, R&D, purchasing, logistics, etc.), ensuring effective communication and tracking project results.
  • Mitigate risks by resolving and taking into account essential market regulations such as ISO 13485 and MDR
  • Ensuring full compliance with Standard Operating Procedures, including Quality Manual and Quality Procedures.
  • Becoming a subject matter expert for Trelleborg Medical Solutions to be a consultative sales professional for our customers
  • Positioning Trelleborg as the contract manufacturer of choice for our current and prospective customers.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Information Technology/IT

Software Engineering

Graduate

Proficient

1

70565 Stuttgart, Germany