Manager Global Product Development (f/m/d) - 24 months

at  Hartmann

8HADB, Baden-Württemberg, Germany -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate07 Aug, 2024Not Specified09 May, 2024N/AMolding,Design Control,Medical Devices,Sterilization,Medical Technology,Biocompatibility,Extrusion,Processing,Polymers,Wound CareNoNo
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Description:

At HARTMANN, we’re all in to help, care, protect and grow. We support healthcare professionals, that they can focus on what really matters: to positively impact people´s life. We realize solutions that make a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make.
Join our team as

QUALIFICATIONS:

  • Completed studies in natural science/engineering (e.g. medical technology, polymer technology / engineering) with focus on polymers /plastics and the associated production technologies
  • Experience in the design and processing of polymeric materials, extrusion & injection molding
  • Experience in project collaboration and/or project management
  • Experience in the field of wound care and medical devices
  • Knowledge of the medical device’s regulation and the associated subject areas (e.g., application, design control, biocompatibility, clinical evaluation, risk management, sterilization, CE conformity, FDA, etc.)
  • Fluent in English and German

Responsibilities:

  • Idea generation for new products and technologies
  • Development of new products in compliance with relevant regulations and standards
  • Management and leadership of projects throughout the development lifecycle including Design Reviews, Technical Reviews and Project Gate Reviews within the Innovation and Development areas of the Wound Care division
  • Preparation and presentation of project status at all levels of the company
  • Technical responsibility for a dedicated product assortment in the field of negative pressure wound care
  • Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs
  • Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements
  • Ensuring product compliance to all relevant rules and guidelines


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Hospital/Health Care

Pharma / Biotech / Healthcare / Medical / R&D

Health Care

Graduate

Proficient

1

89522 Heidenheim an der Brenz, Germany