Regulatory Affairs Specialist 192 193
il y a 2 semaines
We are seeking a highly motivated and detail-oriented Regulatory Affairs specialist to join our pharmaceutical company. The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of pharmaceutical products globally (internationally).
Group 10 Responsibilities:
Submission and Approval Process:
Preparation and submission of Manufacturing License Application (MLA) Preparation and submission of Technical/Site Transfer Applications Preparation and submission of Marketing Authorisation ApplicationsLifecycle Maintenance:
Preparation and submission of documentation for post-approval applications including, but not limited to, Variations, Renewals, MAH Transfers/COAs, LabelingCompliance:
Monitor and maintain up-to-date knowledge of national, European, and International guidelines/legislation Ensuring compliance with all regulatory processes, in readiness for both internal and external audits Ensuring compliance with the regulations of the assigned Countries within European and International RegionsCommunication:
Act as a liaison between the pharmaceutical company and the regulatory agencies Support internal requests for information
Group 12 Experience:
5-8 years of relevant experience in Regulatory Affairs Internationally Lifecycle maintenance experience Experience with: MLA, MAA, CTD, Variations, Renewals, Labeling Applications Experience working with European Regulatory Authorities Experience with software packages and databases (Microsoft Office Suite, Veeva Vault (or comparable EDMS), LorenZ, Trackwise, PromoMat etc.) Good organizational skills and communication skills Ability to prioritize and deliver high-quality work Experience in people management/coordination is a plus Experience in promotional/non-promotional activities is a plus
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Regulatory Affairs Specialist 169
il y a 4 semaines
Courbevoie, France ProductLife Group Temps pleinWe are seeking a highly motivated and detail-oriented Regulatory Affairs specialist to join our pharmaceutical company. The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of pharmaceutical products globally (internationally). Group 10...
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