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Regulatory Affairs Specialist (Senior)
Eingestellt von Michael Bailey Associates - Munich
Gesuchte Skills: Client, Consultant
Projektbeschreibung
SENIOR REGULATORY AFFAIRS SPECIALIST, BASEL, CONTRACT
We are working with a Pharmaceutical company in Basel, Switzerland in order to identify a Regulatory Affairs consultant who would be available for a full time Contract role that pays a competitive Hourly rate.
- Required experience is 3- 10 years experience in a pharmaceutical, biopharmaceutical or medical device regulatory affairs department, other life science sectors will also be considered (for example agrochemical).
- English is the only language requirement.
The role has overall responsibility for the management, organisation and delivery of regulatory submissions to Health Authorities on an Global basis, including Europe, America, Asia and South America. This broad managerial role also gains responsibility in the maintenance & regulatory compliance for drugs with minimal supervision. Our client boasts an organised, professional environment that has a positive social atmosphere.
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 contact details or a 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,
Frank
Michael Bailey Associates GmbH
Job Code: 101638Michael Bailey International is acting as an Employment Business in relation to this vacancy.
We are working with a Pharmaceutical company in Basel, Switzerland in order to identify a Regulatory Affairs consultant who would be available for a full time Contract role that pays a competitive Hourly rate.
- Required experience is 3- 10 years experience in a pharmaceutical, biopharmaceutical or medical device regulatory affairs department, other life science sectors will also be considered (for example agrochemical).
- English is the only language requirement.
The role has overall responsibility for the management, organisation and delivery of regulatory submissions to Health Authorities on an Global basis, including Europe, America, Asia and South America. This broad managerial role also gains responsibility in the maintenance & regulatory compliance for drugs with minimal supervision. Our client boasts an organised, professional environment that has a positive social atmosphere.
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 contact details or a 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,
Frank
Michael Bailey Associates GmbH
Job Code: 101638Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Organisation/Management