Regulatory Project Manager (m/f/d) (100%)


Regulatory Project Manager (m/f/d)



Roche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, Roche Diagnostics International AG in Rotkreuz, we are looking for a

Regulatory Project Manager (m/f/d) 100%

Tasks & Responsibilities:

  • Manages regulatory responsibilities associated with the development, support, and deployment of the Company’s non-medical and medical device software products
  • Manages development and implementation of regulatory strategies and plans to support the timely introduction of new products and the possible preparation and review of government submissions to achieve timely and cost-effective clearance/approval. Provides information for maintaining registrations and listings
  • Monitors and assesses domestic and international Regulatory developments (e.g. Federal Register publication/notices, FDA and EU guidelines, etc.) related to the Company’s products
  • Reviews product labelling to ensure conformance with applicable regulatory requirements and/or approved product claims. Review promotional materials. May serve as a contact with affiliates to achieve international registration of products
  • Frequent contact with external resources and contacts at various management levels concerning operations or scheduling of specific phases of projects
  • Provide Expertise in Software as a Medical Device (SaMD), MDR, and IVDR and related regulations and guidance documents in U.S., Europe, Canada, and APAC. For example, 21st Century Cures Act and related FDA guidance documents, Medical Device Regulation (MDR), EU guidance documents, IEC 62304, ISO 13485, ISO 14971, AAMI TIR45, AGILE development, etc. 

Must haves:

  • Minimum bachelor or master degree in engineering or biomedical engineering
  • At least 5 years of experience in regulatory affairs working within medical device
  • Experience with software, SaMD, working knowledge of software and software development
  • Strong understanding of US regulations and FDA
  • Profound knowledge of EU guidance documents
  • Experience with MDR
  • Experience with submissions for US and EU
  • Hands-on experience in stakeholder management
  • MS Office applications skills

Our offer:

  • Hybrid workplace model (minimum 1 day onsite)
  • Modern workplace with beautiful meeting zones
  • The chance to get involved in one of the most successful pharmaceutical companies in the world and to be a part of multiple international regulatory projects
  • Close and varied cooperation with various internal and external stakeholders 


If you would like an insight into the detailed job description, we look forward to receiving your complete application documents by e-mail to Ms Selina Schumacher ( 

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