Absolvent - Rozvojový propram
Core
Graduate development program to train future Qualified Persons (QP) in pharmaceutical quality, GMP compliance, and regulatory documentation.
Role type
Junior pharmaceutical quality specialist (graduate development program)
Builds
Pharmaceutical quality systems and regulatory compliance for drug manufacturing
Domain
Life sciences / Pharmaceutical manufacturing
Required skills
Master's degree in Pharmacy, Medicine, Veterinary Medicine, Chemistry, Pharmaceutical Chemistry, Technology, or Biology; Ability to learn complex scientific and regulatory information; Attention to detail; Analytical thinking; Native Czech; English B2
Preferred skills
Prior experience in QP activities or pharmaceutical quality; Knowledge of GMP, pharmaceutical quality systems, or regulatory requirements
Technologies
GMP, EU GMP, Pharmacopoeia, SÚKL regulations
Responsibilities
Gain practical experience in pharmaceutical quality processes and active pharmaceutical ingredient quality control; Participate in drug documentation review and compliance with EU GMP and pharmacopoeia requirements; Support GMP activities including internal/external audits, inspections, and supplier qualification; Contribute to quality management systems including deviation handling, change control, CAPA, and risk management; Monitor regulatory changes affecting drug production and batch release; Prepare daily and monthly reports; Travel for audits within Czech Republic and occasionally to Poland
