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Quality engineer

Solothurn
Johnson & Johnson
Ingenieur Qualitätssicherung
EUR 115’000 pro Jahr
Inserat online seit: 28 April
Beschreibung

Duration of the contract: Initially until 31st Dec (likelihood of extension)

Hours per week: 40 Hours, hybrid working (3 days onsite, 2 days home office)

Essential: Previous experience within Pharma or Medtec is strongly preferred, technology transfer, quality and supply chain - fluent English and either German, French, Dutch is desirable

Imagine your next project driving quality excellence within the world's most comprehensive orthopaedic and neurological business. As a Quality Engineer, you will be the vital link between quality compliance and our global Service Centers, ensuring that every repair and service project meets the highest standards for the patients who depend on them.


Roles and Responsibilities

You will be the primary point of contact for quality and compliance aspects for Worldwide Service Centers, focusing on cost-improvement and technology transfer initiatives.

This will involve:

* Ensure general compliance support for consistent and correct execution of QS procedures at DPS Service Sites.
* Be the local main point of contact for quality and compliance aspects related to transformation initiatives and transfer projects.
* Collaborate with Service Operations and other Supply Chain representatives to ensure global harmonization of service processes.
* Partner closely with stakeholders to ensure new initiatives at local Service Centers are implemented as per local and global quality requirements.
* Coordinate and support resolution for all nonconformances, CAPAs, and audit observations related to Installation and Services.
* Conduct data-driven analysis and potentially lead a small team of regional quality coordinators.


How to Succeed

You are a quality-minded professional with a technical background and a passion for process harmonization in regulated environments.


You Will Also Bring

* Master Degree in Engineering or a relevant technical field.
* 4-6 years of experience in a Medical Device environment.
* Strong experience in regulated ISO 13485 industries.
* Proficiency in English AND fluency in either German, Spanish, or Dutch.
* Proven experience in Quality, Manufacturing, or Service and Repair.
* Specific experience with Technology Transfer or Supply Chain projects.
* Lean Six Sigma Green/Black Belt or Project Management Certification (asset).
* Experience with EtQ, Trackwise, Salesforce, or ERP systems (beneficial).


Benefits

This role offers a very competitive hourly rate. This contract will run for initially until 31st Dec with a high likelihood of extension based on performance and project needs.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are.

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