Regulatory Affairs and Pharmacovigilance Specialist
Zentiva
About this role
The Regulatory Affairs and Pharmacovigilance Specialist at Zentiva supports regulatory compliance and pharmacovigilance activities for the company’s OTC portfolio, ensuring submissions and reporting align with national requirements. This is a fixed-term role contributing to maintenance of regulatory systems and collaboration with internal stakeholders and external partners to uphold product quality and compliance.
Skills
Qualifications
About Zentiva
zentiva.comWe develop, produce, and deliver high-quality, affordable medicines to more than 100 million people across Europe.
Recent company news
Advent InternationalZentiva, a leading European generics pharmaceutical company, announces sale from Advent to GTCR
Sep 11, 2025
European Pharmaceutical ReviewEuropean generics firm Zentiva sold in $4.8bn private equity deal
Sep 16, 2025
ReutersPrivate equity firm Advent to sell generic drugmaker Zentiva to GTCR
Sep 11, 2025
Fierce PharmaChicago private equity firm inks €4.1B purchase of former Sanofi generics unit Zentiva: FT
Sep 11, 2025
Bloomberg.comGTCR in Talks for Private Debt to Fund Bid for Drugmaker Zentiva
Aug 27, 2025
About Zentiva
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
Unlock Company Insights
View leadership team, funding history,
and employee contacts for Zentiva.
Salary
$0
per year
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