Trainee Qc Npi

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

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 in Germany are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”

Severely disabled applicants will be given special consideration if they are equally qualified.

Cilag AG is an international production company of the pharmaceutical division Janssen of the Johnson & Johnson Group and manufactures pharmaceutical and medical products as well as chemical agents (APIs) for the global markets at its production site in Schaffhausen. Thanks to our innovative products, processes and technologies, Cilag AG is today one of the leading pharmaceutical companies in Switzerland and at the same time a strategic launch and growth site.

Within the Quality Control (QC) department, we seek a dedicated personality - entry immediately or as agreed on.

**Main Tasks**
- Coordinate and plan the introduction of new products into QC.
- Review and implementation of test methods for new products.
- Create and review GMP documents for new products.
- Review of analytical data.
- Coordinate non-conformances, corrective actions (CAPAs) and changes (change control management) related to the introduction of new products.
- Support documentation for new product registration.

The offered job as a trainee in the QC NPI team offers university graduates an ideal entry opportunity for a responsible GMP position in the pharmaceutical industry. Interfaces to numerous local and global departments (such as the development department, various QC departments and production) as well as the work with new products on site make the daily activities extremely interesting and varied.

Your Profile

In addition to an analytical thinking and structured way of working and strong team and communication skills, you can tackle challenges in a solution-oriented and systematic way, you can solve complex and multi-layered tasks and set your priorities in a correct manner. In addition to your assertiveness, you are ready to take responsibility and enjoy driving projects forward.

**Qualifications**
- You successfully completed your science or technology studies, preferably with a focus on the pharmaceutical, (bio-)chemical or biotechnological fields, or you have some experience as a chemical or biological laboratory assistant in quality control, preferably in a GMP-environment.
- You have very good project management skills.
- You have very good organizational and communication skills, a customer-oriented approach and «can do» mentality.
- You have very good knowledge of analytical methods.
- Experience in the review of analytical data and GMP documents and in dealing with eLIMS and the Empower laboratory system are beneficial.
- You are fluent in German and English.

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**Primary Location**
Switzerland-Schaffhausen-Schaffhausen
- **Organization**
Cilag AG (8562)

**Job Function**
Quality

**Requisition ID**
2206029276W