Medical Device Assembler

Fluid Biomed is an innovative medical device startup developing the world’s first bioabsorbable stent for the treatment of brain aneurysms. Our mission is to transform neurovascular care and improve patient outcomes worldwide. As we progress toward clinical and regulatory milestones, we are growing our manufacturing team.

We are seeking a hands‑on, detail‑oriented Medical Device Assembler (Operator) to support the assembly and inspection of our implantable devices. This role will operate within a cleanroom environment, following GMP and ISO 13485 standards. The Operator will assist with product builds, quality checks, and documentation to ensure devices meet high standards for safety and performance.

• Assemble medical devices using hand tools and microscopes according to work instructions and specifications.
• Perform in-process and final inspections of sub‑assemblies and finished devices.
• Record assembly steps and inspection results in batch records.
• Follow cleanroom protocols and GMP procedures to maintain a sterile environment.
• Support basic cleaning, packaging, and lab activities.
• Communicate any defects, deviations, or equipment issues to supervisors.
• Assist with routine equipment checks and tool setup when trained.
• Maintain a clean, organized, and compliant workspace.

• High school diploma or equivalent is required. Post‑secondary technical training (such as a technical diploma or associate degree) in a relevant field is an asset.
• At least 1 year of experience in assembly, manufacturing, or hands‑on work in a regulated or precision‑based environment.
• Strong manual dexterity and ability to work under magnification.
• Basic understanding of safety, cleanliness, and documentation requirements.
• Ability to follow detailed instructions accurately.
• Basic computer skills: e.g. data entry, use of inspection / test software, ability to follow digital traceability systems, standard Microsoft applications.
• Ability to recognize defects and to document non‑conformances.

• Prior cleanroom or medical device assembly experience.
• GMP or ISO 13485 training.
• Understanding / working within regulated environments: ISO 13485, GMP, or equivalent standards.
• Experience with microscopes and fine assembly tools.
• Familiarity with documentation and quality inspection practices.
• Familiarity with assembly processes and packaging techniques.
• Experience in lean manufacturing, 5S or continuous improvement methodologies — to help optimize process efficiencies.

Work is performed on‑site in an office and cleanroom setting in Calgary, Alberta. Full‑time role with standard weekday shifts – minimum 6‑month term with potential for longer term position. Candidates must be legally entitled to work in Canada.

Fluid Biomed is committed to diversity and inclusivity in the workplace.