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:        

　　Routinely perform moderately-complex to complex processes according to Standard Operating Procedure (SOP).

　　Specific responsibilities include bioreactor sampling activities, cleaning equipment, steaming equipment, and prepping equipment.

　　Strict adherence to GMP regulations.

　　Qualifications:

　　Associate degree in related area

　　1 year of Manufacturing or Operations experience

　　Biotech US/DS manufacturing experience, preferably cell culture.

　　Understanding of measurements, calculations and the metric system

　　Basic GMP knowledge.

　　Understanding of Electric Batch Records, DeltaV, and LIMS.

　　Availability for Day 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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