Functions of the company belonging to
Scientific Area
Roche is market leader in the areas of oncology, virology, and transplant and world leader for in vitro diagnostics.
Once the product is ready, the commercial department guarantees its final success, assuring its proper introduction on the Italian market. Working in the commercial unit includes activities of customer care, market research and analysis, new trends identification, examination of competitors…and much more!
The Medical Affairs department is the medical-scientific reference of excellence, devoted to the creation and the disclosure of clinical data. It works in special collaboration with the scientific community, to the benefit and protection of patients, in line with the corporate principles of ethics as well as corporate objectives and values.
The Clinical Operations department plans and leads clinical studies for the good of patients, satisfying scientific, clinical, regulatory and commercial needs, in line with development and business plans.
Our passion drives us in the development of innovative products and solutions every day. To make sure that our patients do benefit from our products, it is fundamental that health workers are given correct scientific information. This is why Marketing is a strategic department in Roche, to ensure that our success and our progress are conveyed effectively.

In Roche, Production & Manufacturing guarantees the supply of critical health products for patients all around the world. Our diversified portfolio of pharmaceutical products includes innovative and biotechnological drugs, developed for several areas of therapy and for multiple doses..

In every Roche site, we abide by strict quality standards at all organizational levels, as for example clinical trial, plants’ technology, occupational safety or a place’s safety. The quality department provides the supervision and the optimization of our systems, in order to reach and maintain excellent qualitative standards.

The strategic department of Market Access aims at assuring patients of the access to innovative medicines, today and tomorrow without delays or regional differences. The department endeavours to find all the elements promoting access, adoption and recognition of the value of a medicine on the market, guaranteeing the system’s sustainability.

The Regulatory Affairs department supports Research & Development teams as well as those teams focusing on the life cycle of the product, developing and implementing regulatory strategies, registration procedures as well as the rules linked to all the stages of drug development.

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