Jt573 - Quality Engineer I

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:  Develops, modifies, applies, and maintains standards for software systems quality operating methods, processes, and procedures.
Conducts evaluation of software systems activities including requirements, design, development, documentation, integration, test, verification, and validation.
Provides verification and validation of software system requirements, traceability, and testability.  Work with peers to address process changes to existing work instructions and/or standard operating procedures.
Qualifications: Bachelor's degree in engineering 1 to 3 years of relevant experience  Process and Computerized Systems Validation Experience in FDA regulated industries Excellent verbal and written communication skills (English and Spanish).
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