{"id":1148637,"url":"https://alion.io/job/viatris-regulatory-affairs-executive-central-regulatory-affairs-cra-europe","title":"Regulatory Affairs Executive - Central Regulatory Affairs (CRA), Europe","company":{"id":706446,"name":"Viatris","domain":"viatris.fi","url":"https://alion.io/company/viatris","size_band":"1001-5000","is_staffing_agency":false,"is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":88,"open_postings":30,"ghost_share":0,"stale_share":0.267,"repost_share":0,"time_to_fill_p50_days":69,"computed_at":"2026-09-24T05:45:00Z"}},"role":"Public Policy","role_family":"Public Policy","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Lisbon, Portugal"],"countries":["PT"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":24000,"max_usd":43000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":29},"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-09-23T16:39:33Z","employer_posted_date":"2026-09-23","last_verified_at":"2026-09-24T08:14:28Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"Mylan, Lda.Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.\nWe have been included on number of award lists that demonstrate the impact we are making. \nOur Story\nAt VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.\nViatris empowers people worldwide to live healthier at every stage of life.\nWe do so via:\nAccess - Providing high quality trusted medicines regardless of geography or circumstance;\nLeadership - Advancing sustainable operations and innovative solutions to improve patient health; and\nPartnership - Leveraging our collective expertise to connect people to products and services.\nOur global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.\nFor those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world.\nThe Role & What You Will Be Doing\nThis is an exciting opportunity for an experienced Regulatory Affairs professional to play a key role in managing regulatory activities across Europe. You will work with cross-functional teams, affiliate partners, and health authorities to support product registrations, lifecycle management, and regulatory compliance.\nEvery day, we rise to the challenge to make a difference, and here’s how the Regulatory Affairs Executive - Central Regulatory Affairs (CRA), Europe role will make an impact:\nKey responsibilities for this role include:\nManage regulatory activities for a portfolio of pharmaceutical products across Europe.\nPrepare and submit regulatory applications, variations, renewals, and other lifecycle management activities.\nSupport new product registrations through European and national regulatory procedures.\nCollaborate with European affiliate teams to ensure successful implementation of regulatory strategies.\nMaintain regulatory databases and documentation to ensure ongoing compliance.\nBuild strong relationships with internal stakeholders and external business partners.\nSupport interactions with regulatory authorities and contribute to responses to health authority queries.\nMonitor regulatory developments and assess their impact on the product portfolio\nAbout Your Skills & Experience\nFor this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:\nA degree in Pharmacy, Biotechnology, Life Sciences, or a related scientific discipline.\n2-3 years of Regulatory Affairs experience within the pharmaceutical industry.\nKnowledge of European regulatory procedures and post-approval lifecycle management.\nA Master's qualification in Regulatory Affairs would be advantageous.\nStrong communication and stakeholder management skills.\nExcellent organisational skills and attention to detail.\nFluent English, both written and spoken.\nAt Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.\nAt Viatris, we offercompetitivesalaries, benefitsandan inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.\nViatris is an Equal Opportunity Employer.","description_format":"text","description_chars":4279,"description_truncated":false,"requirements":{"experience_years_min":2,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"master","optional":false},"security_clearance":false,"languages":[{"language":"English","level":"Advanced (C1)","optional":false}]},"benefits":[],"hiring_locations":[{"name":"Germany","iso":"DE","kind":"region"},{"name":"France","iso":"FR","kind":"region"},{"name":"United Kingdom","iso":"GB","kind":"region"},{"name":"Austria","iso":"AT","kind":"region"},{"name":"Belgium","iso":"BE","kind":"region"},{"name":"Bulgaria","iso":"BG","kind":"region"},{"name":"Croatia","iso":"HR","kind":"region"},{"name":"Czech Republic","iso":"CZ","kind":"region"},{"name":"Denmark","iso":"DK","kind":"region"},{"name":"Finland","iso":"FI","kind":"region"},{"name":"Hungary","iso":"HU","kind":"region"},{"name":"Ireland","iso":"IE","kind":"region"},{"name":"Italy","iso":"IT","kind":"region"},{"name":"Netherlands","iso":"NL","kind":"region"},{"name":"Norway","iso":"NO","kind":"region"},{"name":"Poland","iso":"PL","kind":"region"},{"name":"Romania","iso":"RO","kind":"region"},{"name":"Spain","iso":"ES","kind":"region"},{"name":"Sweden","iso":"SE","kind":"region"},{"name":"Switzerland","iso":"CH","kind":"region"},{"name":"Estonia","iso":"EE","kind":"region"},{"name":"Greece","iso":"GR","kind":"region"},{"name":"Iceland","iso":"IS","kind":"region"},{"name":"Latvia","iso":"LV","kind":"region"},{"name":"Liechtenstein","iso":"LI","kind":"region"},{"name":"Lithuania","iso":"LT","kind":"region"},{"name":"Luxembourg","iso":"LU","kind":"region"},{"name":"Malta","iso":"MT","kind":"region"},{"name":"Portugal","iso":"PT","kind":"region"},{"name":"Slovakia","iso":"SK","kind":"region"},{"name":"Slovenia","iso":"SI","kind":"region"}],"hiring_excludes":[],"relocation_offered":false,"industries":["Clinical Research","Health Care"],"lifecycle":[{"event":"open","at":"2026-09-23T16:39:33Z"}],"liveness":{"score":90,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.903,"p_room":1,"age_days":0,"expected_fill_days":69,"reasons":["conf:1","velocity","win:early","comp:junior,brand"],"computed_at":"2026-09-24T05:45:00Z"},"pay":null,"html_url":"https://alion.io/job/viatris-regulatory-affairs-executive-central-regulatory-affairs-cra-europe","json_url":"https://alion.io/job/viatris-regulatory-affairs-executive-central-regulatory-affairs-cra-europe.json","meta":{"generated_at":"2026-09-24T19:38:42Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers"}}