Supplier quality engineer Jobs in Pentling

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

Since entering the market in 2000, Thermo Fisher Scientific GENEART GmbH has become one of the world's leading specialists in the production of synthetic genes and in Synthetic Biology. The company provides key technologies for the development and production of new drugs, services for the improvement of proteins ( industrial enzymes, antibodies) or for the construction of cells for complex biological processes ( for use in cell therapies). Today, GENEART is a wholly owned subsidiary of Thermo Fisher Scientific Inc, the world leader in serving science. We enable our customers to make the world healthier, cleaner and safer - that is our mission!

Have a look at this video to get to know more about the work we are doing at GENEART :

For the support of our Team, we are looking for a

Discover Impactful Work

As part of the Quality Systems Team at Thermo Fisher Scientific Inc., you will have a unique opportunity to support processes that are essential for the quality of our products and enable a reliable manufacturing workflow. You will achieve this by collaborating closely with other functions and departments to identify solutions for diverse challenges and, at the same time, ensure strict compliance to the Quality Management System.

A day in the Life

• Review and evaluate complaints and deviations together with functional teams and support the development of corrective actions.
• Ensure the functionality and consistency of documentation by supervising the Document Management System
• Collaborate with subject matter experts to evaluate process change requests and provide guidance throughout the change workflow
• Provide Quality-related Trainings to Site Staff and promote our exceptional Quality Culture.
• Conduct and document Risk Assessments and internal Audits of the site’s processes to ensure adherence to quality standards.
• Lead and Support Projects to Improve the Quality Management System, driving innovation and excellence.

Keys to Success

Education

Experience

Knowledge, Skills, Abilities

What we offer