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Regulatory Affairs Specialist, Basel, Life Science, Contract
Eingestellt von Michael Bailey Associates - Munich
Gesuchte Skills: Client
Projektbeschreibung
We have an opportunity to join the Regulatory Affairs Operations team of a global life science company in Basel.
The role is on a Contract basis and offers life cycle management and regulatory maintenance responsibilities across Europe, Middle East and African regions. English is the only language requirement, there is an hourly rate of 50-55 Chf available for the role and the position is available on a Contract basis until the end of the year with a likelihood of extension into 2017.
The role requires a Bachelor's degree in Life Science (eg Chemistry, Biology, Pharmacy or equivalent) and 1 year of direct experience of working in a Regulatory Affairs department for a life science company.
The position provides training and responsibilities to ensure our client's life science products are being maintained to global health standards.
Responsibilities include: assisting in product renewal writing, coordination/collection/storage of documentation needed for Health Authority (HA) submissions, undertake regulatory database entry activities and interacting with internal departments/Affiliates.
Our client is looking for an individual who matches the progressive company culture and so holds flexibility within the provided requirements. We hope the role will be of interest to you and understand that further information may be required prior to an application to the end Life Science company. If you wish to apply via this website or email me, then I would be pleased to answer any questions you may have and provide further details on request.
Kind regards,
Michael Kellitt
Michael Bailey Associates AG
Job Code: 111039
Key words: Pharmaceutical, Drug Regulatory Affairs, Regulatory Affairs, DRA, RA, API, Veterinary, Vet, Biological, Biotech, Pharma, Medical Devices, Regulatory Affairs Manager, Senior, eCTD, Reg Ops, CMC
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
The role is on a Contract basis and offers life cycle management and regulatory maintenance responsibilities across Europe, Middle East and African regions. English is the only language requirement, there is an hourly rate of 50-55 Chf available for the role and the position is available on a Contract basis until the end of the year with a likelihood of extension into 2017.
The role requires a Bachelor's degree in Life Science (eg Chemistry, Biology, Pharmacy or equivalent) and 1 year of direct experience of working in a Regulatory Affairs department for a life science company.
The position provides training and responsibilities to ensure our client's life science products are being maintained to global health standards.
Responsibilities include: assisting in product renewal writing, coordination/collection/storage of documentation needed for Health Authority (HA) submissions, undertake regulatory database entry activities and interacting with internal departments/Affiliates.
Our client is looking for an individual who matches the progressive company culture and so holds flexibility within the provided requirements. We hope the role will be of interest to you and understand that further information may be required prior to an application to the end Life Science company. If you wish to apply via this website or email me, then I would be pleased to answer any questions you may have and provide further details on request.
Kind regards,
Michael Kellitt
Michael Bailey Associates AG
Job Code: 111039
Key words: Pharmaceutical, Drug Regulatory Affairs, Regulatory Affairs, DRA, RA, API, Veterinary, Vet, Biological, Biotech, Pharma, Medical Devices, Regulatory Affairs Manager, Senior, eCTD, Reg Ops, CMC
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung