• Bachelor’s degree in Engineering or Science; Master’s degree is an asset

• Minimum two years’ relevant experience and/or training related to systems engineering

• Knowledge of medical device technology, applicable quality and safety standards, and regulations ( In particular ISO 60601-x)

• Demonstrated ability to deal with a fast-paced environment, high levels of ambiguity, multiple concurrent projects, and conflicting assignments

• Demonstrated initiative, attention to detail, customer focus, and commitment to ongoing process improvement

• Experience with requirements specification and traceability

• Knowledge of product life-cycle management • Experience with project management a plus