Boehringer Ingelheim is a global pharmaceutical company dedicated to innovation in health solutions for humans and animals, driven by a diverse workforce of over 53,000.
Ingelheim am Rhein, Rhineland-Palatinate
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On-site · Kelowna
The Therapeutic Specialist is responsible for achieving district sales targets and executing multi-channel customer plans through exceptional engagement. They act as a customer orchestrator, collaborating with cross-functional teams to deliver value and maximize patient access to products.
Hybrid · Burlington
The Head of Quality Medicine will lead and evolve the Canadian Medicine Quality Management System while driving a risk-intelligent, data-driven approach to compliance. They will also coach the quality team and serve as a strategic partner to local and global leadership to ensure patient safety and regulatory excellence.
Hybrid · Burlington
The National Medical Science Liaison drives scientific dialogue and establishes peer-to-peer relationships to educate stakeholders on diseases and assets. They are responsible for mapping key stakeholders, executing engagement plans, and generating insights to inform strategic decision-making.
On-site · Burlington
The Manager of Field-Based Medicine leads and manages a team of Medical Science Liaisons to support therapeutic area scientific objectives and regional medical affairs activities. They are responsible for stakeholder engagement, budget oversight, and the professional development and performance management of their team.
On-site · Brampton
Lead the design, transformation, and analysis of complex clinical trials and real-world data to support drug development and registration. Act as a product owner for data science aspects and provide strategic insights to cross-functional teams.
Hybrid · Brampton
The Data Science Co-Op will collaborate with business teams to analyze datasets and design analytical solutions to drive data-driven decision-making. Responsibilities include data preparation, modeling, product development, and translating business ideas into actionable analytical insights.
Hybrid · Brampton
The Project Manager Co-op will support the Data Science team by coordinating internal conferences and tracking project tasks. They will also assist with meeting coordination, reporting needs, and general administrative project support.
Hybrid · Burlington
The Senior Sourcing professional will drive commodity strategies, manage supplier relationships, and negotiate contracts to optimize global spend and productivity. They will also act as a business partner to align procurement activities with stakeholder needs and mitigate sourcing risks.
Hybrid · Brampton
The intern will support the in-house video production team through all phases of development, including planning, filming, and post-production. They will also assist with project management tasks such as scheduling, tracking deliverables, and coordinating stakeholder feedback.
On-site · Brampton
The fellow will participate in therapeutic area development, strategic alignment, and the execution of medical and brand tactics. They will also support publication management, engage with key external experts, and lead research projects to improve medical affairs processes.
Hybrid · Brampton
Lead US regulatory strategy for assigned development projects and marketed products throughout their lifecycle, including FDA interactions, submissions, labeling, and regulatory risk management. Advise global and US cross-functional teams, monitor regulatory developments, and ensure US regulatory considerations support compliant development and business objectives.
On-site · Brampton
The role involves executing disease state awareness initiatives for Obesity and MASH, including managing consumer campaigns, educational programs, and social media activations. You will also lead cross-functional teams, manage agency relationships, and monitor market trends to refine brand strategy and tactical implementation.
On-site · Montréal
The Associate Director manages specialists to drive sales performance for the diabetes portfolio and develops business plans for key accounts. They are responsible for coaching, talent development, and ensuring consistent application of company policies across the district.
Hybrid · Brampton
The Senior Associate Director acts as the Quality and Compliance expert to drive GvP/GcP standards across the drug and device lifecycle. They lead inspection preparations, manage quality management systems, and provide strategic consultancy to ensure regulatory adherence and patient safety.
Remote · Ridgefield, Connecticut, United States
The physician will lead pharmacovigilance and risk management activities for marketed and investigational compounds on a global scale. They will chair internal asset benefit-risk teams and represent the company during interactions with global health authorities.
Remote · Ridgefield, Connecticut, United States
The Patient Safety Physician is responsible for global pharmacovigilance and risk management activities for marketed and investigational compounds. They lead cross-functional asset benefit-risk teams and represent the company in interactions with global health authorities.
Hybrid · Brampton
The Director will lead the strategy, analytics, and quality monitoring for patient support programs across the entire portfolio. They are responsible for managing vendor relationships, ensuring compliance with regulations, and driving performance improvements through data-driven insights.
Hybrid · Brampton
The role involves leading the global Simulation Hub to provide strategic and technical leadership in statistical methodology for clinical development. You will drive the adoption of scalable simulation tools and collaborate across functions to maximize the probability of technical and regulatory success.
Hybrid · Brampton
The intern will collaborate with IT and research scientists to analyze business needs and develop, test, and deploy IT solutions. They will also be responsible for conducting data curation and generating reports to support research activities.
On-site · Brampton
The Senior Research Fellow will represent nonclinical safety in project teams, advising on testing strategies, dose selection, and toxicological assessments from discovery to regulatory submission. They will also provide scientific leadership, mentor staff, and ensure compliance with international regulatory standards for neuroscience and eye health assets.
