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Regulatory Affairs CMC Specialist, Junior, Basel, Contract
Eingestellt von Michael Bailey Associates - Munich
Gesuchte Skills: Client, Support
Projektbeschreibung
We have an entry level opportunity to join a major pharmaceutical company in Basel with limited commercial experience required.
Our client is searching for a life science professional with good English speaking skills, 3 months - 4 years prior commercial experience in life science regulatory affairs and a Graduate/Post degree in a life science subject to join their global CMC team in Basel. An hourly rate of 40-45 Chf is available for the role, the position is full time, onsite in Basel on a contract basis until the end of the year, the job title of the role is 'Regulatory CMC Associate Manager'.
The Regulatory CMC Associate Manager is provided supervision in order to assist in the timely preparation of high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies. Other activities may also include assisting in product renewal writing, coordination/collection/storage of source documentation needed for direct submission to HAs, regulatory database entry activities and more. If you are able to start a new role in February or March in Basel, hold a life science degree and have gained some commercial experience in regulatory affairs via direct or indirect exposure from drug development, quality, pharmacovigilance, medical affairs or clinical research departments then please do not hesitate to apply for this position.
We understand that you would wish to know more about the role on a day to day basis before submitting an application, however please feel free to submit your contact details via this website and I will happily cover any questions you may have regarding the role, there is also a job description available on request.
Kind regards,
Michael
Michael Bailey Associates AG
Job Code: 109
Key words: Regulatory Affairs, RA, DRA, Biotech, Biopharmaceutical, Medical Device, Graduate, Chemistry, Biology, MAA, Chemical Manufacturing and Control, CMC, Regulatory Affairs Officer, Senior Regulatory Affairs Officer, Regulatory Affairs Specialist, eCTD, MRP, DCP
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Our client is searching for a life science professional with good English speaking skills, 3 months - 4 years prior commercial experience in life science regulatory affairs and a Graduate/Post degree in a life science subject to join their global CMC team in Basel. An hourly rate of 40-45 Chf is available for the role, the position is full time, onsite in Basel on a contract basis until the end of the year, the job title of the role is 'Regulatory CMC Associate Manager'.
The Regulatory CMC Associate Manager is provided supervision in order to assist in the timely preparation of high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies. Other activities may also include assisting in product renewal writing, coordination/collection/storage of source documentation needed for direct submission to HAs, regulatory database entry activities and more. If you are able to start a new role in February or March in Basel, hold a life science degree and have gained some commercial experience in regulatory affairs via direct or indirect exposure from drug development, quality, pharmacovigilance, medical affairs or clinical research departments then please do not hesitate to apply for this position.
We understand that you would wish to know more about the role on a day to day basis before submitting an application, however please feel free to submit your contact details via this website and I will happily cover any questions you may have regarding the role, there is also a job description available on request.
Kind regards,
Michael
Michael Bailey Associates AG
Job Code: 109
Key words: Regulatory Affairs, RA, DRA, Biotech, Biopharmaceutical, Medical Device, Graduate, Chemistry, Biology, MAA, Chemical Manufacturing and Control, CMC, Regulatory Affairs Officer, Senior Regulatory Affairs Officer, Regulatory Affairs Specialist, eCTD, MRP, DCP
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges