Beschreibung
Senior Associate (m/f/d)
Reference: -en
Start: asap
Duration: 6 MM++
Main tasks:
- 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
Main qualifications
- 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
- English fluent
Main advantages:
- We will create a candidate profile containing your strengths and potential and thus increase your chance of being placed in a position
About us:
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.
My contact at Hays:
My contact person:
Marija Tomas
Referencenumber:
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