Junior Global Program Regulatory Manager, Basel, Contract PT

We have a Junior level opportunity to join a Regulatory Affairs and Quality Assurance project with a global pharmaceutical company in Basel to ensure the electronic documentation of regulatory and quality actions are being compliantly entered into their operating systems (Documentum and TEDI). English is the only language requirement, the role is on a Part Time basis from 3pm - 7pm (other times also considered) in order to interact with the Project Leaders located in Texas, USA. The contract is on a 6 month rolling basis and pays an hourly rate of 40 Chf.

The position requires at least 6 months of commercial experience in the life science sector and to have had some experience with a Regulatory Affairs Operations System. Responsibilities of the role include tracking submissions through the Documentum system and supporting the Biotechnology Technical Developmentplease feel free to request further information to gain a more holistic understanding of the role on a daily basis, there is also 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. If you wish to apply via this website or to email me through LinkedIn or XING, then I would be pleased to answer any questions you may have and provide further job details on request.

Kind regards,

Michael Kellitt

Michael Bailey Associates AG

Job Code: 109

Key words: Regulatory Affairs Operation, Graduate, Regulatory Operations Specialist, Documentum, TEDI, DRA, Biotech, Biopharmaceutical, Medical Device, MAA, CMC, Regulatory Affairs Officer, Regulatory Affairs Specialist, eCTD

Michael Bailey International is acting as an Employment Business in relation to this vacancy.