The Supplier Quality Engineer provides overall quality assurance in management of select contract manufacturing sites engaged in the production of Apollo’s products.   As the primary liaison with partner manufacturing and supplier organizations, the Supplier Quality Engineer manages the quality specification and quality improvement programs, performs audits/assessments, inspection technique support, verification/validation activities, root cause analysis, CAPA and change management. 

 

The successful candidate will possess:

·       A minimum of a Bachelor's degree , preferably in an Engineering, Life Science, or a related discipline

·       2+ years experience in the medical device industry with a preferred background with Class II devices.

·       FDA and ISO 13485 knowledge

·       Auditing experience is required. Certification including ASQ CBA, ASQ CQA or RABQSA-QMS Auditor is preferred.

·       Strong communication, teamwork, and problem solving skills will be needed

·       Knowledge in root cause analysis skills

·       Experience or knowledge with machining manufacturing processes

·       Six Sigma, Lean, or ASQ Certification and trainings an asset

·       This position will require up to 30-50% travel