Regulatory Affairs Manager - (Swiss Submissions, home-based) (m/w/d)

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Job available in additional locations Frankfurt am Main, Germany| Denmark| Greece| Switzerland| Serbia| Slovakia| Romania| Hungary| Ireland| Lithuania| Ukraine| Slovenia| Spain| Italy| Portugal| France| Czechia| United Kingdom| Latvia| Bulgaria| Estonia| Austria| Poland| Croatia| Belgium| Germany| Remote

• Manage client's product portfolio
• Prepare the Swiss submissions based on applications submitted in EU or elsewhere including all documents
• needed for inclusion in module 1 of the eCTD. Perform a quality check on the documentation for suitability for submission to Swissmedic (validation according to Swissmedic requirements).
• Create/update the Swiss Product Information (Information for Professionals and Patient Information as applicable) based on the SmPC approved in the EU or elsewhere. 
• Prepare module 1 documents (forms, locally required documents etc.) based on the documentation provided by Company (e.g., module 1 from the EU submission). Indicate sufficient hyperlinking for Swissmedic purposes.
• Perform/Support submissions activities to Swissmedic through the appropriate electronic gateway and support client during the entire regulatory process.
• Establish and maintain contact with the national regulatory authorities (Swissmedic) on behalf of client
• Assist client's in national regulatory affairs issues and provide advice on national-specific requirements related to clients product(s) 
• Monitor national Regulatory Affairs legislation and continuously inform  client of new or changed national requirements that affect client's products 
• Advise client on current Swissmedic requirements for packaging materials.
• Co-ordinate end to end local activities including artwork and proof reading 
• aRMM submissions, adaptation, and maintenance (translation) 
• Update product information to relevant local HA databases

• A University Degree in Life Sciences is required with 5 to 7 years of industry experience, of which at least 3 years of experience within Regulatory Affairs (registration, development, maintenance)
• Experience of regulatory requirements in countries outside the US and Europe
• Very good knowledge in written and oral English is required, knowledge of any other languages would be an asset
• Experience from leading projects and cross-functional teams
• German language on B2/C1 level

• A strong team player, with the ability to work effectively in a team setting and interact with people of different cultural, seniority and functional backgrounds
• Highly self-motivated and able to drive activities
• Excellent communication skills
• The suitable candidate should demonstrate the values; Care for our patients, for our colleagues and for our company, Ambition, Urgency, Ownership and Partnership
• Ensure exemplary behavior, ethics and transparency within the Company and with regulatory agencies

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IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com