Job Information
Quality Consulting Group Document Control in Cayey, Puerto Rico
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
Support the manufacturing areas in the implementation or update of document and master data changes through the Engineering Change Order (ECO) systems.
Assists in writing and reviewing departmental procedures and is also responsible for the expeditious processing of new SOP's, tracking and initiating Engineering Change Orders and securing completed documentation for all manufacturing areas.
Qualifications:
Minimum an Associate degree or equivalent.
Two (2) years of relevant experience in the regulatory Industry. (Medical Device, Pharmaceutical, Biopharmaceutical)
Preferable experience in documentation control system in a FDA & ISO regulated environment.
Knowledge on Documentation Control Systems.
Demonstrated ability to perform detail-oriented work with a high degree of accuracy.
Planning/organization, time management, and proactive participation.
Proficiency in the use of Personal Computer, scanner and office related equipment.
Proficiency on MS Office (Word, Excel and PowerPoint).
Knowledge of current business systems and application software (MS Office or equivalent).
Fully bilingual (English and Spanish).
On Site
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
Powered by JazzHR
