Company Reviews

Zentiva provides health and wellbeing for all generations, with focus on developing, producing, and delivering high-quality, affordable medicines to more than 100 million people in over 40 countries across Europe and beyond. Zentiva has four manufacturing sites and a broad network of external manufacturing partners. Zentiva employs more than 5,400 unique talents, bonded together by a commitment to the people who depend on our products every day. Visit us at www.zentiva.com.

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Rating Reviews

Rating is calculated based on 5 reviews and is evolving.

Featured Reviews

Quality Control Specialist
3.0
29 December 2025
Not Much Flex Here for Lab Roles
Pros: Job security is good in pharmaceutical manufacturing. The team in the Prague office is generally supportive. You get decent benefits and a stable work environment.
Cons: Work-life balance can be tough with the strict onsite policy. As a Quality Control Specialist, there's almost no hybrid work available. It's a standard 9-to-5, sometimes longer if projects pile up. Doesn't feel modern for work flexibility.
Advice to Management: Consider offering more flexible or hybrid options for roles where it makes sense. Even occasional remote days could really boost morale for the office staff. It's tough competing for talent without it.
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Regulatory Affairs Specialist
3.0
4 March 2026
Career Paths are Hazy for Pharma Specialists
Pros: I've gained solid experience as a Regulatory Affairs Specialist here. The company culture in the Prague office is generally good, and you work with smart people. It's a stable job in the pharmaceutical industry, which is nice.
Cons: Career growth here is pretty limited, especially for experienced professionals. There aren't many clear paths for internal promotion or moving into different roles. You often feel stuck in your current position, which can be frustrating.
Advice to Management: Management needs to create clearer career progression frameworks for all roles, especially for Regulatory Affairs Specialists. Invest in more training and internal mobility programs to keep good talent.
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Regulatory Affairs Specialist
3.0
29 March 2026
Okay if you're onsite, but flexibility is tough
Pros: I gotta say, the team in the Prague office is super supportive. We collaborate a lot on regulatory filings, which is good. They do offer some understanding for occasional appointments if you communicate way ahead, which is a small plus for pharma roles.
Cons: Work-life balance can be tough for a Regulatory Affairs Specialist. There's not much room for remote work or a hybrid schedule. It's mostly onsite, five days a week. This really impacts work flexibility, especially when you have personal stuff going on. I've heard some other areas might have more, but not in our department.
Advice to Management: Consider allowing more hybrid work options, even a couple of days a week, especially for roles like Regulatory Affairs Specialist where some tasks could easily be done remotely. It would really boost morale and help with work-life balance across the pharmaceutical industry.
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Common Questions About Zentiva

What is the typical salary range for a Quality Assurance Analyst at Zentiva in Prague?
What is Zentiva's policy on remote work for pharmaceutical roles in Europe?
What is the typical working culture like for a pharmaceutical professional at Zentiva in Europe?
What is the typical working culture like at Zentiva, especially for roles in pharmaceutical sales within the European market?
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What kind of benefits can I expect as a pharmaceutical professional at Zentiva, particularly for a role in manufacturing in the Czech Republic?
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