On-site · Oakville
Lead the transfer of new products and manufacturing processes from R&D into a cGMP environment while designing and optimizing assembly strategies. Collaborate with cross-functional teams to ensure manufacturability, scalability, and compliance with regulatory standards.
On-site · Oakville
You will lead the transfer of new products from development into a cGMP manufacturing environment, including process design and scale-up. Additionally, you will manage validation activities, equipment procurement, and continuous improvement initiatives to ensure high-quality production.
On-site · Oakville
The QC Technician will execute quality control processes for incoming materials, in-process samples, and final products to ensure specification conformance. They will also collaborate with manufacturing teams to develop inspection criteria, review batch records, and support non-conformance investigations.
On-site · Oakville
The Laboratory Technician will design, optimize, and validate immunoassays while integrating them into automated diagnostic platforms. They are also responsible for performing nanoparticle conjugations, preparing assay buffers, and maintaining rigorous quality control documentation.
On-site · Oakville
You will be responsible for the manufacture and assembly of consumable components for medical diagnostic platforms from raw materials to final packaging. This role involves operating automated equipment, maintaining accurate production records, and collaborating with engineering teams to improve manufacturing processes.
On-site · Oakville
You will design, develop, and verify robotic instruments and fluidic systems within a cross-functional team. Additionally, you will create test methods, manage CAD databases, and ensure product safety and reliability through DFX best practices.