What are the responsibilities and job description for the Sr. Quality Engineer (Medical Device) position at Talentry?
Sr. Quality Engineer (Medical Device)
Tucson, AZ (Relo available!)
Direct Hire. Onsite.
Talentry is looking for a qualified Sr. Quality Engineer to support
our client’s cutting-edge class III medical devices. The right person for this
role will ensure compliance to ISO 13485, 14971, and 21 CFR 820, 803, 806, and
other regulatory paradigms.
This Quality Engineer will develop and implement SOPs,
training, and documentation for more junior members of the team. He or she will
oversee the inspection of subassemblies, components, raw materials, finished
goods, environmental conditions, etc.
This Sr. Engineer will support continuous quality improvement,
and corrective and preventive actions, CAPAs, NCRs, etc. This also includes
active participation in internal and external audits, contribution to the risk management
plans, etc.
This is the perfect job for someone looking to work in the beautiful
scenic Tucson area and be in on the ground floor of a company poised for explosive
growth and success!
Requirements
Requirements:
BS degree, or equivalent, and 5-10 years of experience.
5 years in a medical device environment (Class II/III).
Proven ISO and CFR regulatory experience.
Benefits
Benefits:
95-110k bonus, benefits, and a great work environment!