Zentiva
The ESO Quality QA Specialist manages the quality lifecycle for assigned subcontracted products and provides independent Quality Assurance oversight for suppliers. This role ensures compliance with GMP, GDP, and regulatory requirements while supporting audits, product lifecycle activities, and quality decision-making. The position involves managing deviations, CAPAs, and supplier quality management to maintain high standards of product quality and safety.
Headquarters
Dolní Měcholupy, Prague, Czechia
Company Size
1001-5000 employees
Founded
1488
We develop, produce, and deliver high-quality, affordable medicines to more than 100 million people across Europe.
Zentiva, a leading European generics pharmaceutical company, announces sale from Advent to GTCR
Sep 11, 2025
European generics firm Zentiva sold in $4.8bn private equity deal
Sep 16, 2025
Private equity firm Advent to sell generic drugmaker Zentiva to GTCR
Sep 11, 2025
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
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
View leadership team, funding history,
and employee contacts for Zentiva.
Zentiva didn’t post a salary, so this is our estimate from similar listings.
31% below the average for this role
Chicago private equity firm inks €4.1B purchase of former Sanofi generics unit Zentiva: FT
Sep 11, 2025
QA Lead, Quality Systems
Cellipont Bioservices
Quality Assurance Specialist - ESO Quality Control
Recordati
Quality Assurance Manager (Pharmaceutical)
Servier
Senior Quality Assurance Associate – GMP/GDP Auditing
Travere Therapeutics
FTC- Jr. Quality Assurance Specialist ESO
Zentiva Česká republika
Supplier Quality Specialist
Guerbet