Empleos en Bristol-Myers Squibb
“Vaga para Jr. Regulatory Affairs Analyst na Bristol Myers Squibb, com foco em processos regulatórios da ANVISA, compliance e trabalho em equipe. Requer formação em Farmácia, experiência mínima de 1 ano na área e fluência em português e inglês. Trabalho presencial ou híbrido, com oportunidades de crescimento em empresa farmacêutica global.”
“Permanent on-site role at Bristol Myers Squibb's new Cell Therapy facility in Leiden, Netherlands. Responsible for material movement, logistics, and cold chain handling in a cGMP cleanroom environment. Requires shift work, on-call hours, and adherence to regulatory standards. Ideal for candidates with science or engineering background and experience in temperature-controlled biologics logistics.”
“Bristol Myers Squibb busca un Clinical Research Associate (CRA) para supervisar ensayos clínicos, garantizando calidad, integridad y cumplimiento de protocolos, SOPs e ICH-GCP. Responsable de visitas de cualificación, monitoreo y cierre de sitios, gestión de datos y relaciones con stakeholders. Modalidad híbrida (LI-Hybrid).”
“Field-based Medical Science Liaison (MSL) role in neurodegeneration for DC, DE, MD. Requires MD/PhD/PharmD with neurology expertise, peer-to-peer scientific dialogue, and clinical trial engagement. Compensation: $166K–$201K. Travel required. Full-time position at Bristol Myers Squibb.”
“Senior Director role at Bristol Myers Squibb for International Therapeutic Area Head in Oncology/Haematology or Innovative Medicine. Requires 15+ years' experience, advanced degree (PharmD/PhD/MD), and strategic leadership across Europe, APAC, and ICON. Oversees TA strategy, regional oversight, external partnerships, and cross-functional collaboration. On-site role with hybrid flexibility.”
“Senior Director role at Bristol Myers Squibb for International Therapeutic Area Head (iTAH) in Oncology/Haematology or Innovative Medicine. Requires 15+ years of bio-pharmaceutical experience, deep TA expertise, and strategic leadership across Europe, APAC, and INTERCON regions. Hybrid on-site role with global medical strategy ownership and cross-functional collaboration.”
“Bristol Myers Squibb seeks a QC Biologics Specialist in Cruiserath, Ireland, for drug product/substance release and stability testing under cGMP regulations. Responsibilities include HPLC/UPLC testing, data analysis, OOS/OOT investigations, and documentation. Requires BSc in Biochemistry (or related), regulated lab experience, and strong problem-solving skills. Full-time on-site role with competitive benefits.”
“Bristol Myers Squibb seeks a Clinical Research Associate (CRA) to oversee clinical trial sites, ensuring compliance with ICH GCP, SOPs, and regulatory requirements. Requires 2-3 years of experience in clinical research, strong analytical skills, and proficiency in CTMS, eTMF, and RBM tools. Role involves site monitoring, data integrity verification, and stakeholder coordination. Hybrid work model with onsite presence required.”
“Regular job offer for a Manager, Regulatory Portfolio Management role at Bristol Myers Squibb in Warsaw. Requires ≥3 years in pharmaceutical regulatory experience, Bachelor's in Healthcare-related field, and knowledge of major Health Authorities. Compensation up to 217,268 PLN. On-site role with hybrid flexibility.”
“Permanent QC Bioanalytical Analyst role at Bristol Myers Squibb's Cruiserath Biologics site. Requires 1-2 years' experience in analytical techniques (Aseptic, Cell Culture, Bioassays, ELISA), BSc in Biochemistry, and cGMP compliance. Hybrid work model (50% onsite). Focus on lab operations, data analysis, OOS investigations, and batch release testing.”
“Vaga sênior para Especialista em Área Terapêutica (Cardio) na Bristol Myers Squibb, com foco em engajamento científico com profissionais de saúde (HCPs) para impulsionar adoção de medicamentos. Requer experiência farmacêutica/biotecnológica (8+ anos), habilidades em vendas e gestão de contas, e viagens frequentes (100% do tempo em campo). Inclusiva para pessoas com deficiência.”
“Bristol Myers Squibb seeks a Medical Advisor in Neuropsychiatry to drive UK medical strategy, launch activities, and HTA collaborations. Role requires advanced clinical/scientific degree, preferably in Psychiatry, with Medical Affairs experience. Hybrid work model with onsite presence essential. Focus on transforming mental health treatment through science and strategic initiatives.”
“Permanent QC Analytical Specialist role at Bristol Myers Squibb (Netherlands) requiring a Bachelor's in science, 2+ years of QC experience, and expertise in cell/molecular biology techniques. Hybrid work model (50% onsite) with responsibilities in testing, data review, method transfer, and GMP compliance. Competitive benefits included.”
“Lead complex site contract and budget negotiations for clinical trials at Bristol Myers Squibb. Requires 7+ years in clinical contract negotiation, legal/compliance expertise, and multilingual skills. Position involves governance, training, and process improvement with up to 20% travel. Full-time role based in Warsaw.”
“Senior medical leadership role at Bristol Myers Squibb leading Psychiatry & Neuroscience strategy, shaping patient access and evidence generation. Requires MD/PharmD with Medical Affairs experience, strategic influence on NHS/NICE policies, and team leadership. Hybrid work model with on-site presence expected.”
“Full-time, fixed-term position in Utrecht, Netherlands for a QC Microbiology Specialist at Bristol Myers Squibb. Requires MLO level 4, 2+ years of microbiological testing experience, and shift work. Responsibilities include in-process/final product testing, environmental monitoring, and GMP compliance. On-site role with hybrid eligibility.”
“Regular Data Analytics Engineer position at Bristol Myers Squibb in Warsaw, Poland. Hybrid role requiring Databricks, Power BI, and SQL expertise to build scalable data pipelines, automate workflows, and develop BI tools. Competitive salary up to 234,943 PLN. Focus on data-driven decision-making for commercial teams in life sciences.”
“Scientist, QC Microbiology role at Bristol Myers Squibb Netherlands for a fixed-term contract. Requires 6+ years in microbiology testing/QC in regulated environments, method transfer/validation expertise, troubleshooting, and mentoring. On-site position with responsibilities in GMP compliance, technical documentation, and regulatory inspections. Ideal for candidates passionate about patient impact in oncology/hematology.”
“Engineer Commissioning, Qualification & Validation (CQV) role at Bristol Myers Squibb in Leiden. Requires 1-3 years' experience in pharmaceutical validation (GMP environment), strong problem-solving skills, and knowledge of cGMP/GXP regulations. Hybrid position with no travel. Responsible for IQ/OQ/PQ activities, protocol writing, and ensuring compliance with BMS requirements.”
“Bristol Myers Squibb seeks a Data Engineer for Clinical Operations to design scalable data pipelines, cloud-native solutions, and GenAI-powered applications for cross-study operations and specimen management. Requires 5+ years in data engineering, Databricks expertise, Python, SQL, and cloud platforms. Position is hybrid with competitive compensation ($87,810-$106,399) and comprehensive benefits.”
“Stellenausschreibung für Clinical Research Associate (m/w/d) in Stuttgart, Heilbronn oder Heidelberg. Verantwortlich für Überwachung klinischer Studien, Einhaltung von GCP/ICH-Richtlinien und Datenintegrität. 2-3 Jahre Erfahrung in klinischer Forschung erforderlich. Hybridmodell möglich (mind. 50% vor Ort).”
“Stellenangebot als Therapeutic Area Specialist (m/w/d) für Kardiomyopathie bei Bristol Myers Squibb in Berlin & Südbrandenburg. Verantwortlich für Verkauf innovativer kardiologischer Therapien in Kliniken und Praxen, Stakeholder-Management, Omnichannel-Strategien und digitale Kundenbetreuung. Naturwissenschaftliches Studium oder Pharmareferent:innen-Ausbildung erforderlich.”
“Regular full-time role at Bristol Myers Squibb in Warsaw for Budget Builder Site Contracting. Requires 2-5 years of experience in clinical trial budgeting, FMV principles, and Excel proficiency. Offers 50% hybrid work, compensation up to 218,360 PLN, and direct impact on clinical trial financial frameworks.”
“Position at Bristol Myers Squibb Netherlands for an Associate QC Microbiology role. Requires Bachelor's degree in science, MLO level 4 or equivalent, and 0-2+ years of relevant experience. Responsible for routine microbiological testing, GMP documentation review, and environmental monitoring. Full on-site role with shift work in a regulated environment.”
“Principal Global Trial Associate role at Bristol Myers Squibb (Warsaw) supporting global clinical trials from concept to final report. Requires 4-6 years of experience in clinical research, project management, and regulatory compliance. Hybrid work model (up to 50% remote). Compensation: 239,890-290,697 PLN. Keywords: clinical trials, project management, pharmaceutical, hybrid, regulatory, oncology.”
“Regular job offer at Bristol Myers Squibb for a Protocol Model Document Content Steward in Warsaw. Requires 5+ years in pharma with GCP expertise, Bachelor's in Life Sciences, and skills in ICH guidelines, TransCelerate standards, and tools like Veeva. Hybrid role with compensation up to 356,442 PLN. Focus on clinical trial documentation, regulatory compliance, and cross-functional collaboration.”
“Permanent role at Bristol Myers Squibb's Cruiserath Biologics site for a Specialist in Warehouse, Cryogenics and Logistics. Responsibilities include GMP sampling, raw material storage, inventory management, SOP development, and ensuring regulatory compliance. On-site position with competitive salary, benefits, and focus on patient impact and operational excellence.”
“Health Physicist role at RayzeBio (BMS subsidiary) in Indianapolis. Requires BS in Health Physics/related field, 1+ year experience in radiological protection and EHS compliance. Duties include radiological assessments, safety policy implementation, training, and incident investigations. Full-time position with salary range $97,208-$117,793.”
“Bristol Myers Squibb seeks a Payroll Analyst in Warsaw for accurate, compliant payroll processing across EMEA countries. Role involves vendor management (ADP), data validation, tax compliance, and employee query resolution. Requires proficiency in English, MS Office, Workday, ADP Celergo, and SAP. Hybrid work model (50-50) with relocation near Warsaw office. Competitive salary: 151,560–183,701 PLN.”
“Lead manufacturing operations for cell therapy at Bristol Myers Squibb's new state-of-the-art facility in the Netherlands. Role requires GMP compliance, cross-functional team leadership, and problem-solving in a cleanroom environment. Ideal for candidates with cell therapy manufacturing experience and strong technical skills.”
“Specialist, QA Operations Shopfloor role at Bristol Myers Squibb Netherlands for onsite quality oversight in manufacturing, QC, warehouse, and packout operations. Requires 0-2 years cGMP experience, preferably in biopharmaceuticals or cell therapy. Focus on compliance, discrepancy resolution, and cGMP adherence. Bachelor's degree in science/engineering preferred.”
“Bristol Myers Squibb sucht einen Therapeutic Area Specialist (m/w/d) für Hämatologie & Onkologie in Mannheim, Heidelberg, Karlsruhe und Pforzheim. Verantwortlich für regionale Verkaufsziele, Kundenbetreuung und wissenschaftliche Beratung von Onkologen. Erfordert Pharma-Berater-Status, Verkaufserfahrung und exzellente Onkologie-Kenntnisse. Hybrid-/Remote-Arbeit möglich mit Reisetätigkeit. Attraktive Benefits und Karrierechancen in einem forschungsgetriebenen Unternehmen.”
“Bristol Myers Squibb seeks a Drug Product Associate for its new Sterile Drug Product facility in Cruiserath. Role involves on-floor technical support for vial/syringe fill-finish, CQV, tech transfer, and commercialization. Requires manufacturing experience in regulated environments, adaptability, and problem-solving skills. Competitive salary, benefits, and career growth in a patient-focused, innovative company.”
“Bristol Myers Squibb busca un Material Handler para su nueva instalación de Terapia Celular en Leiden (Países Bajos). El puesto requiere gestión logística de materiales en condiciones controladas y bajo normativas GMP, incluyendo manejo de equipos y documentación en entornos cleanroom. Se valoran conocimientos en cadena de frío, gestión de inventarios y disponibilidad para turnos rotativos, fines de semana y guardias.”
“Praca na stanowisku Managera ds. Dokumentacji Naukowej i Regulacyjnej w firmie Bristol Myers Squibb w Warszawie. Wymaga doświadczenia 2-4 lat w dokumentacji regulacyjnej, umiejętności pisania dokumentów takich jak IB, CSR, protokoły kliniczne. Praca hybrydowa z elastycznymi benefitami. Wynagrodzenie do 249 445 PLN rocznie.”
“Bristol Myers Squibb offers a managerial role in Warsaw for a Manager, Program Management Systems & Infrastructure. The position involves ensuring high-quality project plans, portfolio data, and tool adoption for Program Managers in the pharmaceutical industry. Requires a Bachelor's degree in science/engineering, 1+ years of pharma experience, and expertise in planning tools. Hybrid work model with competitive salary up to 196,318 PLN.”
“Praca na stanowisku Senior Manager - Submission Management w firmie Bristol Myers Squibb w Warszawie. Wymagane 7+ lat doświadczenia w regulacyjnych procesach klinicznych, umiejętności zarządzania zespołem oraz znajomość globalnych standardów regulacyjnych. Wynagrodzenie od 162 775 do 197 245 PLN brutto rocznie. Praca hybrydowa (do 50% zdalnie).”
“Bristol Myers Squibb seeks a Site Contract Specialist in Warsaw to manage clinical trial site contracts and investigator budgets. This role involves negotiating, reviewing, and finalizing agreements while collaborating with cross-functional teams. Requires a Bachelor's degree, clinical trial experience, and strong organizational skills. Hybrid work model with competitive salary up to 218,360 PLN.”
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