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Remote · Alberta, Canada, Chalfont St Giles, England, United Kingdom, New Brunswick, Canada, Nova Scotia, Canada, United States
The Global Regulatory Affairs Portfolio Lead oversees the registration and lifecycle maintenance of a portfolio of radiopharmaceutical products. They provide strategic regulatory leadership, ensure global compliance, and manage interactions with health authorities to support business objectives.
On-site · Saint-Eustache
The process engineer leads engineering and technology projects, managing budgets, schedules, and resource allocation to meet client requirements. They also oversee process improvement initiatives, document operations, and provide technical support to production teams.
Hybrid
Deliver clinical training and workflow support for patient monitoring solutions across acute care environments. Partner with customers and internal teams to ensure high-quality implementation and post-go-live optimization.
Hybrid
The Data Analyst will support commercial operations by analyzing sales performance, pricing strategies, and customer trends to drive revenue growth. They are responsible for developing dashboards, automating reporting, and collaborating with cross-functional teams to improve operational efficiency.
Remote · Alberta, Canada, Ontario, Canada, Quebec, Quebec, Canada
Coordinate and deliver objective-based system training and education support for clinical customer accounts. Develop relationships with key opinion leaders to standardize protocols and support clinical education initiatives.
Hybrid
The Project Manager coordinates the planning, delivery, and installation of medical imaging equipment while serving as the primary liaison for customers. They are responsible for maintaining accurate project milestones, forecasting revenue, and ensuring cross-functional collaboration to meet business objectives.
Remote · Alberta, Canada, Manitoba, Canada, New Brunswick, Canada, Ontario, Canada, United States
The Manager of Regulatory Affairs is responsible for developing and executing global labeling strategies for PDx products, with a primary focus on US FDA compliance. This role involves cross-functional collaboration to ensure labeling is scientifically sound, globally aligned, and supports the entire product lifecycle.
On-site · Montréal
The Field Service Representative is responsible for providing technical service, including installation, calibration, and preventative maintenance for diagnostic imaging and clinical equipment. They must manage repair parts, document service calls, and maintain strong customer relationships to ensure high satisfaction levels.
Remote · Alberta, Canada, British Columbia, Canada, Nova Scotia, Canada, Saskatchewan, Canada, United States
The Director will develop and implement a global pharmacovigilance audit strategy while overseeing audit operations and regulatory inspection support. They will also lead a team of auditors and collaborate cross-functionally to drive continuous quality improvement.
On-site
The Field Service Representative provides direct technical service, including preventative maintenance and repairs, on medical imaging equipment at various hospital and clinic sites. They act as the primary point of contact for customers, ensuring service excellence and managing repair parts cycles to meet business targets.
Remote · Alberta, Canada
The role involves providing clinical expertise and technical leadership to support the implementation and evaluation of ultrasound products. The specialist delivers training, performs product demonstrations, and partners with sales teams to ensure customer success and product adoption.
On-site · Bromont
The role involves working on the production floor to ensure health, safety, quality, and production targets are met while supporting new product introductions. Responsibilities include monitoring production parts, resolving technical issues, and optimizing process documentation.
On-site · Bromont
The role involves managing product compliance, process qualifications, and technical documentation while acting as a technical focal point for factory projects. The incumbent will also coordinate standard work practices and contribute to operational targets regarding safety, quality, and production efficiency.
On-site · Boisbriand
The logistics coordinator will manage the shipment of finished products by coordinating with sales, planning, and production departments. Responsibilities include preparing shipping documents, tracking carriers, and ensuring timely delivery while maintaining accurate production and transport data.
On-site · Bromont
Develop and implement inspection routines on various measurement instruments, primarily CMMs, to support production and tooling goals. Optimize existing routines and standardize programming methods to improve efficiency and technical strategy in metrology.
On-site · Boisbriand
The production operator is responsible for operating and maintaining various production units, including mixers, separators, and automatic sieves. They must also perform packaging tasks, complete production documentation, and ensure quality standards are met.
On-site · Boisbriand
The production operator is responsible for operating atomizers and mixers, including setup, monitoring, and cleaning of equipment. They also handle the packaging of metallic powder and participate in quality control diagnostics.
Hybrid · Montréal
Drive growth for GE HealthCare's Commercial Service portfolio using a hybrid inside and outside sales model for clinics and hospitals. Act as a trusted advisor to align customer operational needs with tailored service solutions and manage territory financial targets.
Remote · ["Dublin, Leinster, Ireland", "Newfoundland and Labrador, Canada", "Prince Edward Island, Canada", "Quebec, Quebec, Canada", "United States"]
Job Description Summary The Senior Director of Regulatory Affairs, Radiopharma serves as a senior global leader within the Pharmaceutical Diagnostics (PDx) Regulatory Affairs organization, reporting into the Global Head of Regulatory Affairs. This role provides end to end regulatory leadership across drug development, registration, lifecycle management, compliance, and CMC for key markets including the United States, while supporting global regulatory strategy, governance, and operational excellence. The Senior Director leads a multi regional team of global regulatory professionals and partne…
Remote · ["New Brunswick, Canada", "Ontario, Canada", "Saskatchewan, Canada", "Turin, Piedmont, Italy", "United States"]
Job Description Summary The Director of Marketed Products, Radiopharma reports to the Senior Director, RA – Radiopharma and is responsible for leading a global team managing all post-approval lifecycle activities for radiopharmaceutical products across worldwide markets. This role ensures regulatory compliance, drives forward-looking lifecycle and portfolio optimization strategies, enables the efficient execution of variations, renewals, and maintenance activities while collaborating closely with RA-CMC and NPI teams to support product continuity and lifecycle strategy. Job Description Key Re…
