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Zentiva

Produces branded generic pharmaceuticals in Europe

Quality Specialist Systems

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeAnkleshwar, Gujarat, IndiaNo salary listedIn-person

About the Job

Requirements

  • A degree in pharmacy, human or veterinary medicine, natural sciences, or a similar field.
  • At least 2 years of experience as a Quality Manager in the pharmaceutical industry.
  • Sound knowledge and experience in pharmaceutical manufacturing, development, or testing.
  • Strong knowledge of European Union and German legal and regulatory requirements, including Good Manufacturing Practice, Good Distribution Practice, the German Medicinal Products Act, the German Ordinance on the Manufacture of Medicinal Products and Active Substances, the German Narcotics Act, and the German Medical Devices Act.
  • Knowledge of drug approval.
  • Very good user skills in Microsoft Excel, Microsoft Access, and Microsoft PowerPoint.
  • Business-fluent German and English.

Desired Qualifications

  • Experience as a Quality Manager in a sales- and marketing-oriented pharmaceutical company.

About the Company

Zentiva

Produces branded generic pharmaceuticals in Europe

Zentiva makes branded generic medicines for European markets. Its products are off-patent drugs reformulated and marketed under Zentiva’s brands, delivering the same active ingredients and dosage as original medicines at lower prices. It differentiates itself through a long history as an independent platform under private equity, with a growth strategy built on acquiring brands to expand its European footprint. The goal is to become a leading European branded generics platform and improve access to affordable medicines across its markets.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Prague, Czechia
Founded
2003

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