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Regulatory Associate Pharmaceutical Manufacturing Contract
Eingestellt von Taylor Mclaren
Gesuchte Skills: Support
Projektbeschreibung
Key accountability is to prepare, obtain and maintain regulatory authorisations to support manufacturing related business activities both on and off site.
You will review and respond to requests from sites and worldwide affiliates regarding regulatory matters as well as completing FDA annual reports.
In addition you will assess the regulatory implications of deviations, complaints and change controls.
To be successful you will have a degree in a science discipline and previous experience in a GMP related role eg Quality. You will have a great understanding of current GMP requirements as well as good self-management skills, organisational and interpersonal awareness and excellent written and communication skills.
You should also be effective at building and maintaining great working relationships with internal and external customers globally.
Projektdetails
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Einsatzort:
Lancashire, Vereinigtes Königreich
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Projektbeginn:
asap
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Projektdauer:
6 months +
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Sonstiges