US
0 suggestions are available, use up and down arrow to navigate them
PROCESSING APPLICATION
Hold tight! We’re comparing your resume to the job requirements…

ARE YOU SURE YOU WANT TO APPLY TO THIS JOB?
Based on your Resume, it doesn't look like you meet the requirements from the employer. You can still apply if you think you’re a fit.
Job Requirements of Document Control Coordinator (Entry Level):
-
Employment Type:
Contractor
-
Location:
Carlsbad, CA (Onsite)
Do you meet the requirements for this job?
Document Control Coordinator (Entry Level)
Careers Integrated Resources Inc
Carlsbad, CA (Onsite)
Contractor
Job Title: Document Control Coordinator (Entry Level)
Job Location: Carlsbad, CA
Job Duration: 12 Months (possibility of extension)
Payrate: $23.52/hr. on w2
Duties and Responsibilities:
Job Location: Carlsbad, CA
Job Duration: 12 Months (possibility of extension)
Payrate: $23.52/hr. on w2
Duties and 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.
- 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.
- 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.
- Prior experience with documentation of Life Science or Medical Device products.
- Knowledge of ISO 9001 standard required; knowledge of ISO 13485 is an advantage.
- 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.
Get job alerts by email.
Sign up now!
Join Our Talent Network!