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5 years of experience in Pharmaceutical Industry associate with a GMP background * Good knowledge of the pharmaceutical current best practice in analytical and manufacturing technologies, validation and GMP compliance
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Operational experience in GMP in Quality, Manufacturing, or Quality Control would be an asset. * Experience in GMP audits and inspections
Perform all activities in compliance with GMP/HSE rules and regulatory requirements for each development phase of the product. * A good knowledge of GLP/GMP rules is a plus.
The job holder participates in the necessary training defined for his job, e.g. SOP training sessions, GMP training sessions, projects management, technical/scientific trainings, conferences, etc - Operational GMP or quality experience would be a distinct advantage
Assurer le respect strict des procédures établies et des normes de qualité telles que GMP et ISO 17025. * Vous maîtrisez les standards de qualité tels que GMP, ISO 17025, avec une connaissance approfondie des pharmacopées.
Knowledge of GMP regulations and best qualification practices
Strong knowledge of Good Manufacturing Practices (GMP).
Knowledge of Good Manufacturing Practices (GMP) in a laboratory setting.
Experience: Preferably in CAPEX projects within a commercial GMP facility.
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Snel solliciteren
Proven experience as an independent validation project leader in the pharmaceutical industry, preferably GMP GLP.
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