quality engineer in raron

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job details

raron, valais
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job type
reference number
058 201 50 30
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job description

Care for the world ... start with the individual. This motto inspires and unites the people of Johnson & Johnson. The culture of care is the focus of our corporate philosophy, which is anchored in the Credo. With more than 265 operating companies in more than 60 countries, our 130,000 employees are committed to improving the lives of billions of people worldwide every day.

DePuy Synthes sets new standards as one of the leading developers and manufacturers of innovative orthopedic and traumatology products. DePuy Synthes is a significant growth area within Johnson & Johnson and one of the largest providers of orthopedic implants in the knee, hip, extremities, spine, neurosurgery and trauma markets. And now, we are looking for a temporary Quality Engineer for the next 6 months at the Raron site.

Main Tasks :

- Support and Leadership on local and regional CAPA Actions and investigations

- TMV execution/Approval

- Validation approvals

- Inspection sheet preparation/approval


Education Requirements :

- A minimum of a Bachelor's Degree, preferably in Engineering or related technical field.

Experiences :

- Generally requires 2-4 years related experience.
- Experience working in both an FDA and European regulatory environment is preferred.
- This position will require relevant experience working in manufacturing/operations.
- Technical training and experience using Statistics, Lean and Six Sigma Methodologies is preferred including Measurement System Analysis, SPC, DOEs, Reliability, etc.
- Experience with a proven track record of implementing appropriate risk mitigation.

Interpersonal skills / characteristics:

- Strong knowledge of statistical software packages is preferred with the ability to preview, graph and analyze data and be able to present data that facilitates/drives decision making.
- The ability to perform "hands on" troubleshooting and problem solving is preferred. The ability to think on the feet and providing sound judgment is highly desired.
- Good technical understanding of manufacturing equipment and processes is required.
- Understanding of the NPI (New Product Introduction) process and Process Validation expertise is
- A thorough understanding of GMP/ISO regulations and validation regulations is preferred.
- Advanced knowledge and experience in the areas listed in the Duties and Responsibilities associated with the position.
- Demonstrated project management and project leadership abilities are preferred.

Languages :

- German and English : Very Good

If you are interested in this exciting task in a leading international healthcare company, we look forward to receiving your complete application.