RSO Support - Brindisi, Italia - EUROAPI

Descrizione

Euroapi is looking for a RSO Support to join Quality department in our Brindisi site reporting directly to RSO Manager; you will work on submission to Health Authorities and you will give a key contribution to State of Art activities.

Your Responsibilities

You will:

This is a fixed term contract offer.

Our Company

EUROAPI is focused on reinventing active ingredient solutions to sustainably meet customers' and patients' needs around the world. We are a leading player in active pharmaceutical ingredients with approximately 200 products in our portfolio, offering a large span of technologies, while developing innovative molecules through our Contract Development and Manufacturing Organization (CDMO) activities.

Taking action for health by enabling access to essential therapies inspires our 3,450 people every day. With strong research and development capabilities and six manufacturing sites all located in Europe (Saint-Aubin-lès-Elbeuf and Vertolaye in France, Brindisi in Italy, Frankfurt in Germany, Budapest in Hungary and Haverhill in the UK), EUROAPI ensures API manufacturing of the highest quality to supply customers in more than 80 countries.

EUROAPI is listed on Euronext Paris.

The EUROAPI Italy facility is a vast production site with over 240 workers located in the industrial area of Brindisi with a history dating back to 1966. EUROAPI Italy is specialized in the development and manufacturing of Active Pharmaceutical Ingredients (APIs), including antibiotics, corticosteroids, and other intermediates by large scale fermentation under GMP conditions. The Brindisi site produces approximately 200 tons of different molecules per year and hosts a R&D biotechnological center. It is approved by the main health authorities and owns environment and workplace safety certifications.

Our Requirements

Degree in biochemistry/chemistry/pharmaceutical chemistry/pharmacy/chemical engineering

Preferable a Master degree in regulatory affairs

Understanding of chemistry/analytics

Good English level: both written and spoken language. DMF are in English language. He/she has to interact with international colleagues

At least 1 year experience in a GMP QC laboratory

At least 1 year experience in API regulatory affairs department

Ability to work in team and to establish open and collaborative human relationship

High determination on results achievement and target accomplishment

Your Benefits

Culture & Values at EUROAPI

We bring our culture to life in the way we work every day. Our culture enables career development and talent management, we recognize that how we do things is as important as what we do, and our values set out how we achieve our goals and help us "do it right".

Diversity & Inclusion

EUROAPI is committed to nurturing a culture of diversity and inclusion that contributes to improving innovation, performance, and engagement. We value transparency, mutual respect, and equal treatment of people. For this reason, we are firm in protecting our employees against any forms of discrimination.

Environment, Social and Governance

We strongly believe that the success of our company lies in its capacity to adapt to tomorrow's challenges. Our responsibility as a company is to provide sustainability and resilience to the pharmaceutical value chain.

Apply Today

Find out more about this exciting opportunity, apply today or contact Michaela Perrone.

Do you know someone for this role?

We are accountable for the success of EUROAPI and that means finding the best people that share our values. Refer a candidate today or talk to your HR Business Partner to find out more.