Zentiva is a Pan-European Platform developing, manufacturing and providing high-quality and affordable medicines to more than 100 million people in Europe. Zentiva has 4 wholly owned manufacturing sites and a broad network of external manufacturing partners to ensure supply security. We offer solutions in key therapeutical areas like Cardiology & Circulation, Diabetes, Oncology, Respiratory, CNS and focus on expanding our portfolio in self-care. The company is Private Equity owned, delivering sustainable double-digit growth, with an ambitious 5-year plan for further strong (organic and inorganic) growth across Europe.

We are a team of almost 5,000 unique talents bonded together by our mission to deliver high-quality and affordable medicines to people who depend on them every day. We want Zentiva to be a great place to work, where everyone feels welcomed and appreciated and can be their true selves contributing to the best of their ability. 


Life Sciences

Manufacturing

Pharmaceutical

Zentiva

Steffen Saltofte

Tomas Petrla

Martin Albert

Nicki Kons

Michal Kriz

Josef Matousek

Bruno Maugée

Jana Fischerova

Anant Atal

The Quality Assurance and Regulatory Affairs team at Zentiva ensures that all products meet stringent quality standards and comply with regulatory requirements across Europe. This team meticulously oversees quality control processes, pharmacovigilance, and regulatory submissions to guarantee the safety and efficacy of medicines. By collaborating closely with various departments, they play a crucial role in maintaining the integrity of Zentiva's high-quality product offerings while supporting the company's growth ambitions.

Quality Assurance and Regulatory Affairs

Supply Chain and Logistics

Marketing and Commercial Operations

Quality Assurance and Regulatory Affairs

About

Team members

Other teams at Zentiva

Supply Chain and Logistics

Marketing and Commercial Operations