Carrières

Location: 3505 Laird Rd, Mississauga, ON L5L 5Y7, Canada

Status: Full-time

Position Summary:

This role supports aseptic manufacturing operations by operating and maintaining sterile filling equipment, performing routine cleaning and environmental monitoring, and ensuring all production activities meet strict cleanroom and GMP standards. The position involves troubleshooting technical issues, conducting in-process checks, maintaining accurate batch documentation, and contributing to process optimization and continuous improvement. The role also supports inventory management, validation and qualification activities (IQ/OQ/PQ), and root cause analysis for buffer preparation and aseptic processes. Success in this role requires strong technical acumen, attention to detail, effective communication skills, and the ability to work both independently and collaboratively in a controlled cleanroom environment.

Location: 3505 Laird Rd, Mississauga, ON L5L 5Y7, Canada

Status: Full-time

Position Summary:

We are hiring a Sterile Manufacturing Equipment Maintenance and Validation Engineer to own hands-on technical support for aseptic fill-finish operations (bottle filling and IV bag filling) and to lead execution of cleanroom routine maintenance and validation/requalification activities. You will drive equipment reliability, reduce downtime, and maintain a strong state of control in a regulated environment.

Location: 2400 Skymark Avenue, Mississauga, ON, Canada

Status: Full-time

Position Summary:

This role would support and enhance manufacturing processes for medical devices. This role includes analyzing and improving production workflows, developing process documentation (PMAPs, PFMEAs, qualification plans), designing jigs and fixtures using SolidWorks, and supporting verification and validation activities. The position also involves providing technical support to internal teams and customers, conducting training, and performing occasional on-site service, maintenance, and troubleshooting.

Candidates should have an engineering degree, at least 2 years of medical device manufacturing experience, strong knowledge of FDA/ISO quality and regulatory requirements, excellent problem-solving skills, and the ability to collaborate across teams. Experience with process improvement methods (Lean/Six Sigma), ERP systems, and CAD tools is an asset.