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Regulatory Support for Projects
Eingestellt von Clearsource
Gesuchte Skills: Support
Projektbeschreibung
For one of my best clients I am actively looking for a Regulatory Support for projects for a challenging opportunity in a communicative company leader in its market.
START: ASAP
DURATION: 1 year ( +extension)
LOCATION: Brussels
DESCRIPTION:
As a Regulatory Support for projects you will be in charge of the following tasks:
Primary activities, in close collaboration with EMEA Regulatory Coordinator:
- To perform an internal quality checks of our planning and tracking systems and also on our artworks, identify issues and/or gaps, propose a mitigation plan and support in the execution of it
- To perform an internal quality check on randomly chosen products in order to confirm the quality and/or identify issues and/or gaps, propose a mitigation plan and support in the execution of it
- Analyze internal SOPs in view of the role of the EMEA Regulatory Coordinator, check accuracy across SOPs, versus EU regulations and guidance, versus common practice, identify gaps and/or issues, propose a mitigation plan and support in the execution of it
- To provide support for other, not yet defined projects of quality check, clean up, data entry in systems
SKILLS:
- University degree or similar (such as A1 in Belgium),
- Preferably at least two years of experience in the pharmaceutical industry with knowledge about regulatory affairs
- Experience with project management is an asset
- Good understanding of the end-to-end pharmaceutical life cycle
- Excellent written and verbal English is a must; other European languages are an asset
Interested? Please send me your CV immediately
START: ASAP
DURATION: 1 year ( +extension)
LOCATION: Brussels
DESCRIPTION:
As a Regulatory Support for projects you will be in charge of the following tasks:
Primary activities, in close collaboration with EMEA Regulatory Coordinator:
- To perform an internal quality checks of our planning and tracking systems and also on our artworks, identify issues and/or gaps, propose a mitigation plan and support in the execution of it
- To perform an internal quality check on randomly chosen products in order to confirm the quality and/or identify issues and/or gaps, propose a mitigation plan and support in the execution of it
- Analyze internal SOPs in view of the role of the EMEA Regulatory Coordinator, check accuracy across SOPs, versus EU regulations and guidance, versus common practice, identify gaps and/or issues, propose a mitigation plan and support in the execution of it
- To provide support for other, not yet defined projects of quality check, clean up, data entry in systems
SKILLS:
- University degree or similar (such as A1 in Belgium),
- Preferably at least two years of experience in the pharmaceutical industry with knowledge about regulatory affairs
- Experience with project management is an asset
- Good understanding of the end-to-end pharmaceutical life cycle
- Excellent written and verbal English is a must; other European languages are an asset
Interested? Please send me your CV immediately
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges