Release and disposition of batches, review and verification of batch release documentation according to local procedures and product specific checklist
Ensure compliance for materials manufactured with respect to regulatory and GMP requirements
Reviews and performs QA approval on release relevant documents, Deviations, CAPAs, Change-Controls
Release and disposition of API, DS, DP for commercial and clinical Large Molecules/Small molecules products
Participate as a GEQ Release representative on cross-functional teams and projects with regard to the release process
Master Degree / Bachelor Degree in scientific field and profound experience in relevant industry or equivalent
Experience in the pharmaceutical (small molecules or biotechnology) industry
Sound knowledge of cGMP requirements, EU/FDA regulations and compliance
Experience in clinical trials and/or regulatory is an asset
We will create a candidate profile containing your strengths and potential and thus increase your chance of being placed in a position
Über Hays: With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
Diese Anzeige ist nur für angemeldete User möglich.
Bitte loggen Sie sich ein oder registrieren Sie sich, um sich auf das Projekt zu bewerben.