API is a leading Canadian not-for-profit organization dedicated to accelerating growth in the life sciences sector by overcoming challenges faced by companies and innovators.
Edmonton, Alberta
API is one of Canada’s largest not-for-profit life sciences commercialization organizations. We catalyze growth in the life sciences sector by addressing key challenges that hold companies and innovators back.
On-site · Edmonton
The Specialist, Compliance is responsible for maintaining GMP compliance within pharmaceutical manufacturing operations through effective documentation, deviation management, and change control. They partner with cross-functional teams to ensure all manufacturing activities are fully documented, traceable, and inspection-ready.
On-site · Edmonton
The Production Operator executes manufacturing activities for active pharmaceutical ingredients in accordance with cGMP, SOPs, and safety standards. They are responsible for operating production equipment, maintaining documentation, and ensuring product quality throughout the manufacturing process.
Hybrid · Edmonton
The role is responsible for coordinating planned maintenance and calibration for GMP manufacturing and laboratory facilities. Key duties include managing the asset database, monitoring equipment performance, and ensuring accurate documentation and quality compliance.
Hybrid · Edmonton
The coordinator is responsible for planning and implementing preventative maintenance and calibration schedules for GMP manufacturing and laboratory facilities. They also manage the asset database, monitor equipment performance, and ensure all maintenance documentation complies with quality standards.
On-site · Edmonton
The Specialist manages the lifecycle, qualification, and technical support of analytical laboratory instruments and computerized systems within the QC laboratory. They ensure regulatory compliance, data integrity, and support analytical method transfer and validation activities.
Hybrid · Edmonton
The Senior Microbiologist is responsible for leading microbiology operations, including environmental monitoring, contamination control, and equipment qualification in a GMP-compliant sterile manufacturing facility. They will also provide technical mentorship to staff, perform microbial testing, and ensure compliance with regulatory standards such as FDA, Health Canada, and EU GMP.
On-site · Edmonton
The Industrial Millwright/Electrician will perform installation, commissioning, maintenance, and troubleshooting of GMP manufacturing equipment and facility systems. They will work closely with cross-functional teams to ensure equipment reliability, safety, and compliance within a pharmaceutical manufacturing environment.
Hybrid · Edmonton
The Specialist will support the installation, commissioning, qualification, and ongoing operation of GMP manufacturing equipment and facilities. They will serve as the engineering subject matter expert, ensuring equipment reliability and compliance through technical documentation and cross-functional collaboration.
Hybrid · Edmonton
Manage the full validation lifecycle of hardware and software systems to ensure compliance with cGMP, 21CFR11, and GAMP5 requirements. Oversee facility operations, equipment qualification, and the implementation of electronic quality management and manufacturing systems.
Hybrid · Edmonton
Build and lead the planning, supply chain, and program costing functions from the ground up for pharmaceutical innovation. This includes owning the master production schedule, end-to-end cost modeling from R&D to fill-finish, and GMP materials procurement.
Hybrid · Edmonton
Oversee the full finance function and lead HR and IT departments to support organizational growth and operational excellence. Partner with the CEO to provide strategic financial insight, manage complex revenue streams, and ensure robust internal controls.
Hybrid · Edmonton
Serve as the Subject Matter Expert for the CMPC project, overseeing complex construction, installation, and CQV activities for a pharmaceutical manufacturing facility. Lead the preparation and execution of qualification protocols (IQ/OQ/PQ) and ensure compliance with GMP and safety standards.
