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Zentiva

Produces branded generic pharmaceuticals in Europe

Qualified Person - Distribution

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

About the Job

Requirements

  • A university degree with specialization in chemistry, industrial chemistry, biochemistry, or pharmacy is required.
  • At least 5 years of experience in a quality area in the pharmaceutical industry is required.
  • Strong knowledge of Good Manufacturing Practice and Good Distribution Practice processes and regulations, pharmaceutical quality assurance principles, and regulatory requirements is required.
  • Experience with deviations, complaints, investigations, corrective and preventive actions, change controls, risk assessments, quality agreements, transport and storage excursions, and audit and inspection support is required.
  • Fluency in Czech and English proficiency are mandatory.

Responsibilities

  • Establish, describe, and document the medicinal product distribution system.
  • Release returned goods back into distribution, coordinate recalls, and decide on disposal.
  • Control and complete documentation, control transport conditions, and provide Good Distribution Practice distribution release for products already certified by another EU Qualified Person.
  • Prepare, review, and approve Quality Assurance Agreements.
  • Review and approve risk assessments, change controls, deviation and complaints investigations, and associated corrective and preventive actions.
  • Support investigations to ensure timely evaluation of deviations and complaints and their escalation when needed.
  • Edit, review, and approve Good Manufacturing Practice and Good Distribution Practice documents and internal procedures.
  • Review and approve Product Quality Reviews.
  • Work with electronic systems such as Quality Forward, eDMS, and SAP.
  • Register approved suppliers and distributors and relevant Good Distribution Practice certificates.
  • Serve as the single point of contact for the local health authority regarding Zentiva distribution activities.
  • Support internal, external, and customer audits, and lead or assist during health authority inspections as required.

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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