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Job Description:
We are seeking a Systems or Quality Engineer to be responsible for integrating design procedures templates and guidance documents within our ISO 13485 compliant Quality Management System (QMS). The successful candidate will have a working knowledge of FDA/ISO regulations specifically ISO 13485 (7.3) and 21 CFR 820.30 and the application of Good Documentation Practices. Demonstrate ability in writing quality system procedures. The ideal candidate will have a demonstrated ability to communicate with a wide range of stakeholders including Quality Systems/Risk Project Management Regulatory Affairs Marketing and others.
Responsibilities:
Requirements:
Additional Information :
All your information will be kept confidential according to EEO guidelines.
Remote Work :
No
Employment Type :
Contract
Contract