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Zentiva

Produces branded generic pharmaceuticals in Europe

AD Specialist

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

About the Job

Requirements

  • At least two years of experience in a similar position is advantageous.
  • Computer skills.
  • English language proficiency at an intermediate level or higher.
  • Knowledge of Good Manufacturing Practice rules, environmental protection, occupational health and safety, fire prevention and firefighting, and standard operating procedures.
  • Knowledge of physicochemical analysis laboratory activities.
  • Knowledge of instrumental analyses, including UV-Vis spectrometry, atomic absorption spectrometry, infrared spectroscopy, gas chromatography, and high-performance or ultra-high-performance liquid chromatography.
  • Knowledge of non-instrumental analyses.

Responsibilities

  • Perform physicochemical analyses to verify product quality in compliance with Good Manufacturing Practice, occupational health and safety, environmental management, legal requirements, and corporate standards for medicines.
  • Transfer analytical methods and develop and validate analytical methods for new products.
  • Prepare transfer protocols and reports for transferred products.
  • Perform physicochemical analyses during analytical and technological transfers for new products.
  • Develop and validate analytical methods for transferred new products.
  • Prepare validation protocols and reports for new products.
  • Perform physicochemical analyses for products undergoing technological-process validation.
  • Test products used in clinical investigation studies.
  • Test beta-lactam products.
  • Update analytical methods to the latest editions of international pharmacopoeias.
  • Develop new analytical methods for medicine quality control and cleaning validation in accordance with Good Manufacturing Practice and international pharmacopoeias.
  • Validate analytical methods for finished and intermediate products, including methods used for equipment-cleaning validation and cross-contamination checks, in accordance with Good Manufacturing Practice and international pharmacopoeias.
  • Perform physicochemical analyses and tests on finished products in preparation for stability studies.
  • Perform physicochemical analyses as part of cephalosporin control.
  • Perform analyses during cleaning validation or cross-contamination processes.
  • Perform physicochemical analyses and tests to obtain secondary standards.
  • Participate in investigating and interpreting out-of-specification results.
  • Prepare documentation required for quality dossiers submitted for registration.
  • Prepare technical specifications.

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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