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Product Engineer Cycle Management - Medical Devices

Job in New Iberia, Iberia Parish, Louisiana, 70563, USA
Listing for: medmix
Full Time position
Listed on 2026-07-01
Job specializations:
  • Engineering
    Product Engineer, Medical Device Industry, Biomedical Engineer
Job Description & How to Apply Below
Position: Product Engineer Life Cycle Management - Medical Devices

Product Engineer Life Cycle Management - Medical Devices

Vollzeit

Business Segment:
Drug Delivery

Location:

Stuttgart

medmix is a worldwide leading provider of high-precision delivery devices. We occupy leading positions in the end markets of healthcare, consumer, and industry. Our customers benefit from our commitment to innovation and technological progress, which has resulted in over 900 active patents. Our 14 production sites worldwide and our highly motivated and experienced team of almost 2,700 employees offer our customers uncompromising quality, proximity, and flexibility.

Haselmeier, a part of medmix, has been established in the healthcare market for over 100 years. With around 240 employees, Haselmeier has been a pioneer in the development of injection pens for subcutaneous use since the 1960s. We continue to drive innovations in self-injection pens, from design and manufacturing to packaging and delivery. We have developed solutions in scalable volumes for numerous pharmaceutical partners, always taking into account the latest engineering practices – and we want to continue to develop.

We develop our products with a patient-centered approach. Our injection devices are used in various therapy areas and help patients with diabetes, support the treatment of fertility, and are even an option for gentle cancer therapy.

Job Description
  • Transferring product design-specific development results into series production
  • Maintaining product specifications, design-specific product documentation, and master data for series products and platforms
  • Planning and evaluating design verifications and creating corresponding reports for changes or deviations (including aging stability and biocompatibility)
  • Planning, conducting, and documenting root cause analyses and evaluations of product design, performance, and safety
  • Optimizing series products and LCM-relevant processes
  • Coordinating, organizing, and implementing customer-specific issues such as CAPA, complaints, and deviations
  • Planning and implementing changes to series products
Qualifications
  • Successfully completed engineering studies in medical technology, mechanical engineering, plastics technology, or a related field
  • Several years of professional experience in the development of medical devices
  • Knowledge of relevant quality standards and technical norms
  • Good knowledge of common MS Office products and 3D CAD systems
  • Fluent German and English skills in speech and writing
  • Professional and confident demeanor in contact with customers, suppliers, and partners
Additional Information

At medmix, you will become part of a renowned team. Attractive compensation and numerous additional benefits are of course included. You can expect the following:

  • Flexible working hours within our flexitime model
  • 30 vacation days per year
  • Company pension plan
  • Employee savings plan
  • Subsidy for public transport ticket
  • Pluxee Benefit:
    Prepaid card with monthly top-up
  • Discounts via the apps "Corporate Benefits" and "Benefits me"
  • Regular company events
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