Explore 11 Jobs at Gilead Sciences
Open Positions at Gilead Sciences
Posted 5 days ago
The Specialist I, Quality Assurance (Quality Systems) supports administration, maintenance, compliance, and continuous improvement of Gilead Alberta’s Quality Management System. Responsibilities include supporting regulatory inspections and audits, tracking quality metrics, administering deviation, CAPA, change control, documentation and training processes, and assisting with electronic quality systems.
Key Details
Top Skills Required
Posted 21 days ago
The Regulatory AI Capability Lead will advance operational effectiveness and digital enablement across CMC Regulatory Affairs at Gilead Sciences. The role leads process-improvement and digital initiatives, translates regulatory needs into technology solutions, and drives cross-functional implementation, adoption, and change in a global organization.
Key Details
- full time Jobs
- $158,355 - $204,930 per year
- 8+ years experience
Top Skills Required
Top Benefits
Posted 25 days ago
Gilead is hiring a Senior Maintenance Technician focused on electrical maintenance at its Edmonton site. The role maintains, repairs, troubleshoots, tests, and installs industrial electrical and control equipment, supports production uptime, records maintenance activity, and follows safety, electrical-code, and GMP requirements.
Key Details
- full time Jobs
- 8+ years experience
Top Skills Required
Posted a month ago
The Sr Research Associate in Analytical Development develops and executes analytical methods and experiments to characterize and support process development of novel small-molecule drug substances. The role analyzes and interprets data, documents and communicates findings, and collaborates with cross-functional teams to resolve technical challenges while following quality, safety, and environmental standards.
Key Details
- full time Jobs
- 2+ years experience
Top Skills Required
Posted a month ago
The Associate Director, Quality Assurance – GMP Operations provides senior Quality leadership and direct oversight of GMP manufacturing, QC, and supply chain activities at Gilead’s Edmonton site. Responsibilities include ensuring GMP compliance and inspection readiness, leading quality risk management and product disposition, overseeing quality systems and documentation, and mentoring Quality personnel.
Key Details
- full time Jobs
- 8+ years experience
Top Skills Required
Top Benefits
Posted a month ago
The Associate Director, Public Affairs leads Gilead’s public affairs strategy across Canada, with a focus on oncology, integrated communications, and stakeholder and patient engagement. The role oversees media relations and issues management, supports product launch communications and healthcare policy engagement, and coordinates cross-functional teams, agencies, programs, budgets, and compliance.
Key Details
- full time Jobs
- $158,355 - $204,930 per year
- 8+ years experience
Top Skills Required
Top Benefits
Posted a month ago
The Associate Director, Commercial Operations leads a three-person team and oversees customer-centric commercial analytics, CRM adoption, dashboards, incentive compensation planning, and AI/data governance for Gilead Canada. The role partners across business, technology, and global teams to support sales execution, product launches, strategic planning, and continuous improvement.
Key Details
- full time Jobs
- $147,305 - $190,630 per year
- 10+ years experience
Top Skills Required
Top Benefits
Posted 2 months ago
The Senior Research Associate I, QC Chemist supports a 24/7 manufacturing operation by conducting routine and non-routine analyses of raw materials, intermediates, and finished products, and reviewing results for accuracy and compliance. Responsibilities also include investigations, equipment inspection and maintenance, troubleshooting, protocol preparation, and participation in laboratory training and improvement activities.
Key Details
- full time Jobs
- 2+ years experience
Top Skills Required
Posted 2 months ago
Develops and optimizes chemical processes and multi-step synthetic routes for manufacturing drug substances, including laboratory experimentation, scale-up, purification, and quality analysis. The role supports clinical studies and commercialization through process strategy, technical documentation, cross-functional collaboration, and adherence to safety, quality, and environmental standards.
Key Details
Top Skills Required
Posted 2 months ago
The Senior Scientist, Process Development develops and scales chemical processes for manufacturing drug substances, planning and analyzing experiments, optimizing synthetic routes, and supporting clinical and commercial production. The role also prepares technical documentation, supports cGMP manufacturing, collaborates across functions, and contributes to project strategy and team management.
Key Details
- full time Jobs
- 2+ years experience
Top Skills Required
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