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Regulatory Affairs CMC Specialist, Biotech, Basel, Contract
Eingestellt von Michael Bailey Associates - Munich
Gesuchte Skills: Client
Projektbeschreibung
We have an opportunity available to join the Regulatory Affairs CMC department of a global pharmaceutical company in Basel.
Our client is searching for a candidate with over 2 years of commercial experience in biotech (Development/Quality/RA) and with at least 3 months experience within life science regulatory affairs. English is the only language requirement, the position is at the Manager level and offers the chance for you to take on additional responsibilities across the regulatory life cycle process (from development to registration and post approvals). The role is on a full time Contract basis from May to October 2016 and for an hourly rate of 50-55 Chf.
Our client is looking for the right person who matches the positive company culture and accordingly holds flexibility within the provided requirements; please feel free to request further information to gain a better understanding of the role on a daily basis, there is a detailed job description available on request.
We hope the role will be of interest to you and understand that further information would be required prior to an application to the end Pharmaceutical company.
Kind regards,
Michael Kellitt
Michael Bailey Associates AG
Job Code: 110
Key words: DRA, Regulatory Affairs, Arzneimittel, RA, Regulatory Affairs Manager, CMC, Chemical Manufacturing and Control, eCTD, Biopharmaceutical, Biotech, Drug Regulatory, MAA, market submissions, market authorisation, Generic, Medical Device, OTC, Pharmaceutical
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Our client is searching for a candidate with over 2 years of commercial experience in biotech (Development/Quality/RA) and with at least 3 months experience within life science regulatory affairs. English is the only language requirement, the position is at the Manager level and offers the chance for you to take on additional responsibilities across the regulatory life cycle process (from development to registration and post approvals). The role is on a full time Contract basis from May to October 2016 and for an hourly rate of 50-55 Chf.
Our client is looking for the right person who matches the positive company culture and accordingly holds flexibility within the provided requirements; please feel free to request further information to gain a better understanding of the role on a daily basis, there is a detailed job description available on request.
We hope the role will be of interest to you and understand that further information would be required prior to an application to the end Pharmaceutical company.
Kind regards,
Michael Kellitt
Michael Bailey Associates AG
Job Code: 110
Key words: DRA, Regulatory Affairs, Arzneimittel, RA, Regulatory Affairs Manager, CMC, Chemical Manufacturing and Control, eCTD, Biopharmaceutical, Biotech, Drug Regulatory, MAA, market submissions, market authorisation, Generic, Medical Device, OTC, Pharmaceutical
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung