Beschreibung
Quality Assurance Associate (m/f/d)
Reference: -en
Start: asap
Duration: 12 MM
Main tasks:
- Responsible for management of batch release documentation (including samples) originated by CMOs
- Prepare batch release documentation for the following review, assemble disposition package and share it with next step of release chain
- Inform stakeholders about completion of disposition activities
- Collect and analyze data supporting goals and department metrics, including overdue release classification
- Serialization checks and tracking activity
- Support local Quality System, including archiving activities
Main qualifications
- Minimum Bachelor's degree, Master degree preferred, in a scientific topic (Pharmacy, Chemistry, Biology, Biochemistry etc.)
- Profound experience in similar position in pharmaceutical or biotechnology industries
- Experience in the pharmaceutical industry (small molecules and/or biotechnology and/or aseptic filling)
- Sound knowledge of cGMP requirements, EU/FDA regulations and compliance is beneficial
- Strong communication skills
- Able to clearly communicate expectations to internal/external customers as well as management
- Drive new processes set up implementation and ad hoc projects
Main advantages:
- A very renowned company
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:
Marc Peter Linder
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