MiRus™ is focused on the design of innovative solutions for treatment of orthopaedic, spine and structural heart disease
Marietta, Georgia
MiRus™ is a privately held medical device company launched in 2016 focused on the design of innovative solutions for the treatment of spinal and orthopaedic degeneration and deformities and structural heart disease. MiRus provides pre-operative, intra-operative, and post-operative solutions utilizing our proprietary alloy, innovative implant designs, groundbreaking procedure solutions and remote physiologic monitoring platforms to improve outcomes over the continuum of care.
Remote · United States
Assist in managing cardiovascular clinical studies by developing study protocols, monitoring plans, and ensuring high-quality data collection. Serve as the primary point of contact between clinical site investigators and the internal team while ensuring compliance with GCP and FDA regulations.
On-site · Brampton
Perform precise hand-sewing and stitching tasks for the assembly of high-quality cardiovascular medical devices. Follow standard operating procedures and quality guidelines to meet production goals in a regulated environment.
On-site · Montréal
The role involves programming and setting up a 5-axis milling cell to produce medical device components. Responsibilities include making real-time machine edits and ensuring parts conform to engineering drawings and quality requirements.
On-site · Montréal
Program and set up CNC Swiss type screw machines to produce medical device components. Ensure parts conform to engineering drawings and quality requirements through precise measurement and adjustment.
On-site · Brampton
The Quality Engineer provides functional support for new product development and product line maintenance using quality engineering and assurance techniques. Key duties include managing CAPAs, conducting audits, and ensuring compliance with federal and industry regulations during manufacturing and distribution.
On-site · Urban agglomeration of Montreal
The role involves supporting the design and development of medical implants and instrumentation through CAD modeling, engineering analysis, and the creation of detailed prints. The engineer will also manage project documentation, including Design History Files and Device Master Records, ensuring compliance with ISO and FDA regulations.
On-site · Urban agglomeration of Montreal
The Manufacturing Associate organizes and executes production workflows in the post-processing department, including assembly and processing of medical devices. Responsibilities include operating equipment, maintaining clean work areas, and completing documentation in compliance with GDP and SOPs.
On-site · Urban agglomeration of Montreal
The Logistics Associate manages the end-to-end logistics process, including planning, execution, and optimization of product delivery. Key duties include maintaining warehouse organization according to OSHA and FDA regulations and coordinating with internal stakeholders to ensure customer demands are met.
On-site · Urban agglomeration of Montreal
The role involves managing and analyzing complex clinical datasets for a TAVR trial to ensure data integrity and regulatory compliance. Key tasks include developing trial datasets, performing quality checks, and generating submission-ready reports for FDA/EMA.
