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11766en
- Contract
- English
- Associate
- Research & Development
- Zug
- Healthcare & Life Sciences
Skills
Regulatory Affairs, SOP, administration, coordination
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About our client
For our client, one of the leading Healthcare & Life Sciences companies based in Basel, Swisslinx is seeking a highly motivated individual to take on a challenging role as a Drug Regulatory Affairs CoordinatorThis is a contract position for initially 10 months with the possibility for extension.
Your mission:
- Ensuring SOP Matrix is maintained and kept up to date
- Assigning appropriate training role for RA associates as requested
- Creation and maintenance of training roles for RA associates
- Resolving training assignment/DQT email notifications related issues
- Organizing RA PRC SP site and maintaining the folders to ensure all of the required documents are archived appropriately
- Acting as the administrator of system used by RA for review of documents and training assessment.
The ideal candidate:
- 3 years experience working within the Pharmaceutical industry, preferably with experience in Regulatory Affairs / Quality
- Basic knowledge of global regulatory/quality requirements and training management
- Understanding of MS applications (Word, Excel, PowerPoint, SharePoint)
- Strong organizational and time-management skills with compliance mindset
Candidates must have a valid Swiss or European permit or work rights to be considered for this position. If you would like to be considered for the role, please apply directly or send your CV to fiona.maqi@swisslinx.com.
We look forward to hearing from you!
For our client, one of the leading Healthcare & Life Sciences companies based in Basel, Swisslinx is seeking a highly motivated individual to take on a challenging role as a Drug Regulatory Affairs CoordinatorThis is a contract position for initially 10 months with the possibility for extension.
Your mission:
- Ensuring SOP Matrix is maintained and kept up to date
- Assigning appropriate training role for RA associates as requested
- Creation and maintenance of training roles for RA associates
- Resolving training assignment/DQT email notifications related issues
- Organizing RA PRC SP site and maintaining the folders to ensure all of the required documents are archived appropriately
- Acting as the administrator of system used by RA for review of documents and training assessment.
The ideal candidate:
- 3 years experience working within the Pharmaceutical industry, preferably with experience in Regulatory Affairs / Quality
- Basic knowledge of global regulatory/quality requirements and training management
- Understanding of MS applications (Word, Excel, PowerPoint, SharePoint)
- Strong organizational and time-management skills with compliance mindset
Candidates must have a valid Swiss or European permit or work rights to be considered for this position. If you would like to be considered for the role, please apply directly or send your CV to fiona.maqi@swisslinx.com.
We look forward to hearing from you!
