Opportunity Description
Our Client, a Medical Devices / Healthcare company, is looking for a Quality Specialist for their Englewood, CO location. Responsibilities:
+ Perform technical writing and editing of quality system documents, including procedures, work instructions, forms and templates to enhance clarity, consistency, and readiness for migration into Windchill.
+ Perform document integration activities, including formatting updates, metadata alignment, revision verification, and reference accuracy.
+ Assist with mapping document attributes, lifecycle states, and approval workflows into Windchill.
+ Support training and onboarding activities related to updated document workflows where needed.
+ Contribute to continuous improvement of documentation practices during system integration.
+ Documentation Quality & Compliance
+ Ensure documents meet applicable regulatory and quality system requirements (21 CFR 820, ISO 13485, MDR as ap...
+ Perform technical writing and editing of quality system documents, including procedures, work instructions, forms and templates to enhance clarity, consistency, and readiness for migration into Windchill.
+ Perform document integration activities, including formatting updates, metadata alignment, revision verification, and reference accuracy.
+ Assist with mapping document attributes, lifecycle states, and approval workflows into Windchill.
+ Support training and onboarding activities related to updated document workflows where needed.
+ Contribute to continuous improvement of documentation practices during system integration.
+ Documentation Quality & Compliance
+ Ensure documents meet applicable regulatory and quality system requirements (21 CFR 820, ISO 13485, MDR as ap...
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