Must Have : Core reliability engineering (Avoid quality / site/asset reliability engineer profiles)

Domain: Medical device/ MedTech domain only

Location: Ottawa, ON

Work Mode: Onsite

Keywords to look in a profile:

Candidates with medical device or regulated hardware experience, strong background in reliability engineering, HALT/HASS/ALT, and statistical modeling (Weibull, lognormal).

Technical Evaluation – Assess expertise in DFMEA/PFMEA, fault tree analysis, accelerated life testing, DOE, and use of data tools (Minitab/JMP required; Python/Matlab/R preferred).

Regulatory Knowledge – Verify familiarity with ISO 13485, ISO 14971, FDA 21 CFR 820, EU MDR/IVDR, IEC 60601, IEC 62304, IEC 62366‑1, ISO 10993, and ISO 17025.

Responsibilities:

• Working with R&D, quality assurance and manufacturing teams to develop reliability requirements (including requirements cascade),...