Jt859 - Associate Manufacturing Process Technician

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.
• Packaging/Manufacturing environment and Equipment operation.
• Loading components, moving pallets of components, equipment operation

• High school/GED + 1 year of work or military experience or Associate degree
• Skills: Biotech DS manufacturing experience, preferably solution prep; understanding of measurements, calculations and the metric system ; basic GMP knowledge.
• Understanding of Electronic Batch Records
• solid employment history and proficiency with basic technology such as laptops and tablets (including iPads) are required.
• Prior exposure to GMP-regulated industries, electronic batch records, DeltaV, or LIMS is a plus but not required, as training will be provided.
• Nice-to-have experience includes packaging, warehousing, and assembly.
• Candidates must be open to starting on a day shift and later transitioning to a rotating 12-hour schedule as part of a 24/7 operation. 
• Rotating 12-hour day shifts (anticipated: 6:00 AM – 6:30 PM)
• Rotating Week 1: 38 hrs., Week 2: 48 hrs.

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.