Develop, implement, and maintain a risk management process in the Quality System that conforms with ISO 14971 across product realization by providing strategic and tactical direction.
Candidate will help with risk management documents that are being converted into new templates, collaborate with teams (risk management files)
Skills Looking For
Work on Risk management documents; help in converting old templates to new templates to match new requirements.
Exp in the EU MDR activities.
Strong Project Management skills.
Quality Med Device exp is great.
Risk documentation experience
Education And Experience
Engineering degree is required (Mechanical, Electrical, or Bio-medical only)
Ideally 3 to 5 years of experience; candidate must be able to justify their resume and able to speak in detail of their experience.
Interview Process
Phone screening followed by panel video interview.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Project Management and Information Technology
Industries
Medical Equipment Manufacturing, Biotechnology Research, and Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Intellectt Inc by 2x