Jt413 - Quality Associate Ii

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: Coordinate, perform and manage Laboratory Equipment, Software, Method Transfers, Change Control.
Assist and supports in Chemical testing.
Coordinate Laboratory Equipment, Method transfer and software validation.
Performs and supports Laboratory Change Control.
Performs changes to procedures applicable to the process.
Coordinate/Support/ Perform validations (Laboratory Equipment, Test Method, Test Method transfer, etc.)
in a timely manner.
Manage and use applicable Software Application.
Coordinate, participate and perform communication, meetings or teleconference with company departments or facilities, as required.
Able to work under minimum supervision and to handle multiple tasks at the same time.
Able to prepare and/or provide training, when required.
Support in internal and external audits.
Qualifications: Bachelor's degree in sciences (Biology, Chemistry, Biotechnology, etc.
), or Engineering Three (3) years of previous experience in Quality and Manufacturing Word, Power Point, Excel, Trackwise Laboratory, software and/or test method validation experiences Availability for 1st shift 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