Jt572- Manufacturing 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: Plan, write, implement, and review the Computer Systems Validation documentation.
Make sure that all computer-based systems are operating as intended (with documents to prove it) and meet regulatory requirements.
Determines systems software requirements.
Work across a variety of software lifecycle activities as determined by project needs.
Generate and execute qualification protocols and reports. Organize and maintain project status progress detail.
Work with process owners to address process changes to existing work instructions and/or standard operating procedures.
Qualifications: Bachelor degree in Engineering or related field One (1) or (3) three 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.
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