Ingénieur Qualité II

## Ingénieur Qualité IIPostuler:
Sur site:
Fridley, Minnesota, United States of America:
Temps plein:
Offre publiée hier:
Date de fin : 27 octobre 2026 (Il reste 6 jour(s) pour postuler):
R79727

We anticipate the application window for this opening will close on - 27 Oct 2026

Chez Medtronic, vous pouvez entamer une longue carrière d’exploration et d’innovation tout en aidant à soutenir l’accès aux soins de santé et l’équité pour tous. Vous dirigerez avec détermination en surmontant les obstacles à l’innovation dans un monde davantage connecté et compatissant.
** Journée type
** The Quality Engineering function partners across manufacturing, operations, and quality teams to improve product and process performance through risk identification, prevention, and continuous improvement. This team focuses on strengthening quality systems, advancing First Time Quality (FTQ) practices, reducing manufacturing and process variation, and supporting compliant, scalable operations that prioritize patient safety and product quality.
This Hybrid Flex position is based at Rice Creek - West and requires onsite presence four days per week. 25% travel is required.
As a Quality Engineer II, you will drive initiatives that improve manufacturing and business process quality by reducing risk, improving process stability, and embedding First Time Quality principles across operations. This role partners with cross-functional teams to implement sustainable quality improvements, strengthen compliance, and support projects that enhance operational performance and product quality.

** Responsibilities may include the following and other duties may be assigned:
*** Lead projects that reduce factory escape risks across internal and external manufacturing sites.
* Drive elimination of rework and reprocessing activities to improve process efficiency and value stream stability.
* Define, implement, and enhance First Time Quality (FTQ) programs, metrics, and governance processes.
* Partner with manufacturing and engineering teams to embed quality controls into new production lines and equipment.
* Implement First Time Quality principles within transactional and non-manufacturing processes.
* Support development and maintenance of a compliant, scalable Quality Management System.
* Interpret regulatory requirements, agency guidelines, and internal policies to ensure compliance.
* Manage project activities including planning, risk identification, issue resolution, resource coordination, and communication of project status.  
** Must Have:

Minimum Requirements
***** To be considered for this role, please ensure the minimum requirements are evident in your applicant profile.**
* * Bachelor's degree and 2+ years of relevant experience OR Master's degree.
* Experience supporting quality improvement initiatives within a regulated industry.
* Experience analyzing process performance and using data to drive quality improvements.
* Experience working with quality systems, compliance requirements, or continuous improvement programs.
** Nice to Have*
* * Experience in medical device, pharmaceutical, biotechnology, or other regulated manufacturing environments.
* Experience with First Time Quality (FTQ), Lean Manufacturing, Six Sigma, or continuous improvement methodologies.
* Experience leading cross-functional quality or process improvement projects.
* Knowledge of manufacturing risk management, process validation, or quality engineering tools.
* Experience establishing and monitoring quality metrics and performance indicators.

Pour les diplômes de baccalauréat obtenus en dehors des États-Unis, un diplôme qui satisfait aux exigences de la réglementation 8 C.F.R. § 214.2 (h) (4) (iii) (A) est requis.
** Exigences physiques du poste
** Les déclarations ci-dessus…