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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 moving totes, large scale solution prep batching, cleaning equipment, steaming equipment, and prepping equipment.

+ Train on equipment, policies and procedures.

Qualifications:

+ High school/GED + 1 year of work or military experience or Associate degree

+ Biotech DS manufacturing experience (preferably solution prep).

+ Manufacturing experience preferred but not required.

+ Basic GMP knowledge.

+ Understanding of Electric Batch Records, DeltaV, and LIMS.

+ Detail Oriented skills

+ Team Player skills

+ Shift: 3rd shift with 12-hour rotation starting 6:00pm to 6:30am

+ Week 1: Tues – Wed (Thu - Fri off) & Sat – Mon

+ Week 2: Thu – Fri (Tues - Wed off & Sat – Mon off)

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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