Details

Contract

Full-Time

Location

Neuchatel, Switzerland

Department

Life Sciences

Openings

1

Job ID

31870749

Be a part of a revolutionary change! At PMI, we’ve chosen to do something incredible! We’re totally transforming our business, and building our future on smoke-free products with the power to improve the lives of a billion smokers worldwide. With huge change, comes huge opportunity. So, wherever you join us, you’ll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions. It’s so rare in R&D that everything aligns to create the ideal conditions for outstanding work. Right now, at PMI, that’s exactly what’s happening. R&D is the driving force for our bold new vision: to replace cigarettes with a revolutionary portfolio of alternative products. Join us and you’ll have the resources, support and technology you need to break new ground and see ideas come to life. You’ll be surrounded by some of the brightest scientists in their fields, with fast access to subject experts and commercial decision-makers. If you’re creative, courageous and ready to take risks, you can make a huge impact and propel your career in an endless number of directions. Ultimately, by delivering our smoke-free future, your work could change the lives of a billion smokers. Your ‘day to day’ As a Manager Post-Market Regulatory Management you'll lead all aspects of the post-market submissions, reporting or notifications, for CC/RRP and Life Science products, in line with relevant regulatory requirements and internal and external standards. More specifically, you'll • Manage all post-market regulatory submissions for authorized products in line with applicable regulations and/or requirements • Collaborate closely with internal partners to ensure that post-market reports and notifications are complete and prepared following the current good practices and standards • Ensure the maintenance of regulatory databases and departmental filing systems to facilitate accurate and retrievable records of department activities • Represent regulatory in organizational change activities and establish clear process and SOPs for post-market regulatory activities • Keep up-to-date with the current regulations/ guidelines and share the knowledge with the team Who we’re looking for • Degree in life science, with good knowledge of regulatory processes • Minimum 5 years of experience in a Regulatory Affairs position ideally in management of post-market reporting obligations for tobacco and/or pharmaceuticals • Knowledge of US and EU directives, ICH regulation and guidelines • Ability to prepare high quality regulatory submissions • Ability to prioritize and handle multiple tasks in a fast-paced and constantly evolving environment • Previous experience in working within a multi-functional, multidisciplinary and project-team oriented environment to ensure project and business alignment • Proficiency in English, both oral and written What we offer Our success depends on the men and women who come to work every single day with a sense of purpose and an appetite for progress. Join PMI and you too can: • Seize the freedom to define your future and ours. We’ll empower you to take risks, experiment and explore. • Be part of an inclusive, diverse culture, where everyone’s contribution is respected; collaborate with some of the world’s best people and feel like you belong. • Pursue your ambitions and develop your skills with a global business – our staggering size and scale provides endless opportunities to progress. • Take pride in delivering our promise to society: to improve the lives of a billion smokers. PMI is an Equal Opportunity Employer As with many countries, Switzerland has immigration restrictions which will impact the possibility for non-nationals to work in the country. Profiles required for this position may not being specific enough to justify the recruitment of a person outside of Switzerland or countries having agreed upon free movement with Switzerland, please note that in this case a valid Swiss work permit or Swiss or EU-25 EFTA citizenship is required to apply for this position.

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