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Senior DRA Global Labelling Manager, Contract, Basel
Eingestellt von Michael Bailey Associates - UK Contracts
Gesuchte Skills: Client
Projektbeschreibung
We have an exclusive opportunity to work with a leading Pharmaceutical company in Basel on Contract basis to help their Global Regulatory Affairs Labelling operations to meet critical deadlines. This is an exceptional opportunity for an experienced individual with Pharmaceutical experience to provide strategic and operational regulatory labelling input and work in close collaboration with numerous important internal cross-functional teams and external stakeholders.
The role is working on a full time basis, onsite in Basel and pays a competitive Hourly Rate. Please see the following minimum requirements:
- Science based BS or MS with requisite experience and demonstrated capability. Advanced degree (MD, Ph D, PharmD) preferred
-Fluency in English as business language, additional languages advantageous.
-Special expertise and seniority in the listed activities.
-Direct experience (at least 1-6 years) in global labelling for the life science industry.
-Alternatively extensive experience in related areas of the Pharmaceutical Industry or Health Authorities will also be considered.
I hope that the role will be of interest to you and understand that further information may be required before making an application to the end client, please feel free to send either your full name, contact details or a complete CV via this website and I will get back to you with further information on the role and answer any questions you may have. Alternatively I am contactable during normal business hours (and later on request) on direct dial via the below number.
Best regards,
Neha Sharma
MBA Michael Bailey Associates
Job Code: 106517
Key words: Regulatory affairs, RA, DRA, regulatory affairs, regulatory affairs labelling, label, regulatory labelling, Pharma, pharmaceutical, biotech, biopharm, regulatory affairs, regulatory affairs specialist, regulatory affairs officer, regulatory affairs specialist, DCDS, CDS, BSS, International Package Leaflets (IPL), GLC, PSUR
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
The role is working on a full time basis, onsite in Basel and pays a competitive Hourly Rate. Please see the following minimum requirements:
- Science based BS or MS with requisite experience and demonstrated capability. Advanced degree (MD, Ph D, PharmD) preferred
-Fluency in English as business language, additional languages advantageous.
-Special expertise and seniority in the listed activities.
-Direct experience (at least 1-6 years) in global labelling for the life science industry.
-Alternatively extensive experience in related areas of the Pharmaceutical Industry or Health Authorities will also be considered.
I hope that the role will be of interest to you and understand that further information may be required before making an application to the end client, please feel free to send either your full name, contact details or a complete CV via this website and I will get back to you with further information on the role and answer any questions you may have. Alternatively I am contactable during normal business hours (and later on request) on direct dial via the below number.
Best regards,
Neha Sharma
MBA Michael Bailey Associates
Job Code: 106517
Key words: Regulatory affairs, RA, DRA, regulatory affairs, regulatory affairs labelling, label, regulatory labelling, Pharma, pharmaceutical, biotech, biopharm, regulatory affairs, regulatory affairs specialist, regulatory affairs officer, regulatory affairs specialist, DCDS, CDS, BSS, International Package Leaflets (IPL), GLC, PSUR
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung