{"id":1151811,"url":"https://alion.io/job/bristol-myers-squibb-grs-manager-regulatory-affairs-manager","title":"GRS Manager (Regulatory Affairs Manager)","company":{"id":7994,"name":"Bristol Myers Squibb","domain":"bms.com","url":"https://alion.io/company/bms","size_band":"5000+","is_staffing_agency":false,"is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":98,"open_postings":23,"ghost_share":0,"stale_share":0.261,"repost_share":0,"time_to_fill_p50_days":15,"computed_at":"2026-09-24T05:45:00Z"}},"role":"Public Policy","role_family":"Public Policy","seniority":null,"employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Buenos Aires, Argentina"],"countries":["AR"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":48000,"max_usd":138000,"period":"year","method":null,"sample_n":451},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-09-23T18:04:54Z","employer_posted_date":"2026-09-23","last_verified_at":"2026-09-24T22:50:12Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"At Bristol Myers Squibb, our employees often ask, “Who are you working for?”-a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.\nBristol Myers Squibb es un empleador que brinda igualdad de oportunidades. Las personas que apliquen para cualquier vacante, y que estén calificadas para la misma recibirán consideración para el empleo sin distinción de raza, color, religión, sexo, orientación sexual, identidad de género, nacionalidad, edad, discapacidad, condición de veterano protegido, embarazo, ciudadanía, estado civil, expresión de género, información genética, afiliación política o cualquier otra característica protegida por la ley.\nCollaborate with regulatory strategies for submissions of NDA´s and Clinical trials to accelerate new science to patients at the time compliance is respected.\nCollaborate with local country submissions for new registrations in accordance to business need.\nEnsure regulatory compliance at a local level\nMaintain established brands in line with strategy\nLocal team engagement and alignment.\nPosition Responsibilities \nCollaborate with country regulatory strategy for new products registration and life cycle management in alignment with business goals.\nCommunicate regulatory submission dates, regulatory status, nature of changes, track and inform of minor/significant product information changes to all relevant parties\nMaintain strong relationships with other functional areas (i.e., Medical, Supply, Commercial, QA/QC).\nPlan and track activities related to regulatory submissions\nPlan, prepare, submit and follow up new license applications and post approval variations (labeling, CMC)\nResponsible for the in-time review and approval of 100% promotional materials.\nManagement of Health Authority (HA) requisitions.\nIdentify opportunities to improve departmental functions/processes\nDegree Requirements\nScience related degree\nFluent English skills\nExcellent technology profile\nTransparent communication\nTeam Leader\nExperience Requirements\nMore than 7 years in Pharma Industry\nKey Competency Requirements \nUp-to-date regulatory knowledge required to do the job as described above, and experience with new drug development work. \nFluent in English\nGood communication and interpersonal skills\nStrategical agility\nWe hire for skills and capabilities, not just credentials - if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.\nHow We Work\nWhere you work matters - because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.\nSupporting People with Disabilities\nBMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.\nCandidate Rights\nBMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.\nFor roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/\nData Protection\nWe will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.\nAny data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.\nIf this posting is missing required information required by local law or incorrect, contact BMS at  with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.\nR1606295 : GRS Manager (Regulatory Affairs Manager)","description_format":"text","description_chars":4898,"description_truncated":false,"requirements":{"experience_years_min":null,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":null,"security_clearance":false,"languages":[{"language":"English","level":"Advanced (C1)","optional":false}]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Biotechnology","Health Care","Biopharma"],"lifecycle":[{"event":"open","at":"2026-09-23T18:04:54Z"}],"liveness":{"score":90,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.903,"p_room":1,"age_days":0,"expected_fill_days":15,"reasons":["conf:1","velocity","win:early","comp:brand"],"computed_at":"2026-09-24T05:45:00Z"},"pay":null,"html_url":"https://alion.io/job/bristol-myers-squibb-grs-manager-regulatory-affairs-manager","json_url":"https://alion.io/job/bristol-myers-squibb-grs-manager-regulatory-affairs-manager.json","meta":{"generated_at":"2026-09-25T00:03:59Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","usage":{"tier":"crawler","counted_by":"address","units_charged":1,"used_today":89,"day_limit":5000,"remaining_today":4911,"minute_limit":60,"resets_at":"2026-09-26T00:00:00Z"}}}