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Job Requirements of Document Control Coordinator:
-
Employment Type:
Contractor
-
Location:
Carlsbad, CA (Onsite)
Do you meet the requirements for this job?
Document Control Coordinator
Careers Integrated Resources Inc
Carlsbad, CA (Onsite)
Contractor
Job Title: Document Control Coordinator
Location: Carlsbad, CA, 92010
Duration: 12+ months (Possibilities of Extension)
Pay Rate: $23.52/Hour on W2
Job Description Summary:
Essential Duties, Critical Success Factors, Responsibilities, Authorities and Required Interactions:
Job Responsibilities:
Success Factors:
Education and/or Work Experience Requirements:
#sczr2
Location: Carlsbad, CA, 92010
Duration: 12+ months (Possibilities of Extension)
Pay Rate: $23.52/Hour on W2
Job Description Summary:
Essential Duties, Critical Success Factors, Responsibilities, Authorities and Required Interactions:
Job Responsibilities:
- Implement changes based on red-lines and format engineering documents per documentation standards
- Ensure guidelines and definitions are consistently applied across templates and documents.
- Review all documentation for accuracy, completeness and consistency in content, format, files, and authorizations.
- Filing, scanning, copying and electronic notification and distribution of released documentation.
- Store and control archived documentation.
Success Factors:
- Meticulous attention to detail and strong organizational skills.
- Skilled at prioritizing in a demanding and fast paced environment while producing error free work and meeting required deadlines.
- Adept at multitasking and troubleshooting while appropriately addressing issues as they arise.
- Ability to work independently.
- Well versed in good documentation practices
- Team Player – Thrives in a team environment to achieve a shared goal or outcome
Education and/or Work Experience Requirements:
- 2-3 years of relevant experience
- Graduate from a recognized program in QA preferred
- Previous QA and QMS experience
- Previous experience working within a GMP manufacturing environment would be an asset.
- Experience working with Electronic Document Management System.
- Knowledge of ISO 9001 standard required; knowledge of ISO 13485 is an advantage
- Prior experience with documentation of Life Science or Medical Device products.
- Strong word processing skills using Microsoft Office products including application and editing of Word multilevel lists, pagination, headers/footers, tables and track changes.
- Strong communication skills, both written and verbal.
- Experience with design document engineering change orders.
- Knowledge of document control procedures including database storage, maintenance, and revision control.
#sczr2
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