TalentBurst
Document Control Coordinator (Entry Level)
TalentBurst, Carlsbad, California, United States, 92002
Document Control Coordinator
Carlsbad CA 92010
12+ Months
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 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 #TB_PH
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 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 #TB_PH