Contract Documentation Specialist III
Artech, Newark, NJ, United States
Job Title:- Contract Documentation Specialist III
Duration:- 6-month contract
Location:- Branchburg NJ
Payrate:- $45 - $46/ Hour
Job Description:-
Process, edit, verify and route controlled documents within the electronic document management system. Documents include procedures, forms, specifications, test methods and other quality system documents. This role works across multiple functions to ensure the appropriate level of document review and approval to build and maintain robust documentation. Reviews and evaluates low impact changes as Change Manager in the electronic Change Management System (OneTrack).
Education and Experience
" Bachelor s degree and 3 years professional experience in Documentation/ Change Control or Associate s Degree and 5 years of experience in Documentation/Change Control required.
" 5 years of experience in pharmaceutical/Medical Device industry preferred.
" Knowledge of computerized systems for document management, preferably Veeva. Knowledge of Good Manufacturing Practices.
" Computer system knowledge of MS Office and TrackWise.
" Excellent verbal and written communication skills. Ability to work with multiple priorities with minimal supervision.
Duration:- 6-month contract
Location:- Branchburg NJ
Payrate:- $45 - $46/ Hour
Job Description:-
Process, edit, verify and route controlled documents within the electronic document management system. Documents include procedures, forms, specifications, test methods and other quality system documents. This role works across multiple functions to ensure the appropriate level of document review and approval to build and maintain robust documentation. Reviews and evaluates low impact changes as Change Manager in the electronic Change Management System (OneTrack).
Education and Experience
" Bachelor s degree and 3 years professional experience in Documentation/ Change Control or Associate s Degree and 5 years of experience in Documentation/Change Control required.
" 5 years of experience in pharmaceutical/Medical Device industry preferred.
" Knowledge of computerized systems for document management, preferably Veeva. Knowledge of Good Manufacturing Practices.
" Computer system knowledge of MS Office and TrackWise.
" Excellent verbal and written communication skills. Ability to work with multiple priorities with minimal supervision.