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Process Specialist (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Engineering
Projektbeschreibung
297931/8
IHRE AUFGABEN:
-You are responsible for CAPA Management and Root Cause Analysis
-You are responsible for Deviations, Change Control and OOS during the production
-You are responsible for the compilation of documentations
IHRE QUALIFIKATIONEN:
-You have a university degree in Life Sciences (Biotechnology, Engineering, Biology, Chemistry, etc.) or similar qualifications
-You have in-depth work experience in the manufacturing of pharmaceuticals, ideally biopharmaceuticals/aseptic manufacturing
-You are proficient in the use of root cause investigational tools and performing data analyses
-You have profound experience in deviation and change management
-You have extensive knowledge of manufacturing plants and clean rooms as well as knowledge of standard regulations (EU GMP guidelines, CFR, AMWVH, etc.) and comprehensive GMP skills
-You have strong communication skills and the ability to train others on complex processes
-You are an excellent problem solver with strong analytical thinking and documentation skills
-You can communicate both in English (excellent writing skills) and German
WEITERE QUALIFIKATIONEN:
Quality manager
Projektdetails
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Einsatzort:
Northeim, Deutschland
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Projektbeginn:
asap
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Projektdauer:
4 MM
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik