{"id":3439911,"url":"https://alion.io/job/abbott-regulatory-affairs-project-manager","title":"Regulatory Affairs Project Manager","company":{"id":2710,"name":"Abbott","domain":"abbott.com","url":"https://alion.io/company/abbott","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":81,"open_postings":283,"ghost_share":0.004,"stale_share":0.753,"repost_share":0.018,"time_to_fill_p50_days":29,"computed_at":"2026-11-01T06:10:25Z"}},"role":"Management","role_family":"Management","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Beijing, China"],"countries":["CN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":31000,"max_usd":69000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":6904},"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"EU MDR","optional":false}],"status":"live","first_seen_at":"2026-10-29T05:31:17Z","employer_posted_date":"2026-10-29","last_verified_at":"2026-11-02T00:47:36Z","board_verified":true,"closed_at":null,"days_open":3,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":3},"description":"JOB DESCRIPTION:\nThe Opportunity\nThe Regulatory Affairs Project Manager is responsible for leading assigned regulatory projects supporting registration, approval, and lifecycle management of Abbott CRM products in China.\nThe individual will work independently with cross-functional teams and global stakeholders to execute regulatory strategies, manage complex registration projects, and ensure compliance with applicable China regulatory requirements.\nThis role requires strong regulatory expertise, project management capability, and the ability to manage multiple priorities across an evolving product portfolio.\nWhat You'll Work On\nProject Leadership and Cross-Functional Collaboration\nLead assigned regulatory projects and drive execution against agreed timelines, milestones, and business objectives.\nServe as the China regulatory representative for cross-functional project teams, ensuring effective stakeholder alignment and decision-making.\nAnticipate and manage regulatory risks, issues, and dependencies to support successful project outcomes.\nProvide regulatory direction and influence project strategies throughout the product lifecycle.\nMonitor relevant China regulatory requirements, standards, and guidance updates. Assess regulatory impacts and support implementation activities where applicable.\nRegistration & Lifecycle Management\nPrepare and submit regulatory applications for product registrations, renewals, amendments, and other lifecycle management activities.\nCoordinate testing, clinical evaluation, standards compliance, and submission documentation activities.\nAssess and support implementation of product, software, manufacturing, labeling, and supplier changes.\nEnsure regulatory documentation complies with applicable regulations and company procedures.\nRequired Qualifications\nBachelor's degree or above.\n5+ years of Regulatory Affairs experience within medical devices or healthcare industries.\nExperience supporting China medical device registrations and lifecycle management.\nKnowledge of China medical device regulations and NMPA registration requirements.\nExperience managing multiple regulatory projects independently.\nStrong project management, communication, and stakeholder management skills.\nStrong quality compliance ethos.\nCan travel 10-15% of business time\nFluent in English and Chinese.\nPreferred Qualifications\nCRM, cardiovascular, active implantable, or Class III medical device experience.\nExperience working in a global matrix organization.\nThe base pay for this position is\nN/AIn specific locations, the pay range may vary from the range posted.\nJOB FAMILY:\nRegulatory OperationsDIVISION:\nMD Medical DevicesLOCATION:\nChina > Beijing : Rm1201,Sun Palace Building,No.12Taiyanggong Middle Road,ChaoYang District, BeijingADDITIONAL LOCATIONS:\nWORK SHIFT:\nStandardTRAVEL:\nNot specifiedMEDICAL SURVEILLANCE:\nNot ApplicableSIGNIFICANT WORK ACTIVITIES:\nNot 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