Production Associate O1 - LVLM (2nd Shift, M/F, 2pm - 10:30 pm)

Production Associate position in serum manufacturing at Cytiva's Logan, Utah facility. Responsible for operating within quality and compliance protocols to produce pharmaceutical products, working the second shift (2pm-10:30pm). Requires high school diploma and ability to perform physical manufacturing tasks in a controlled environment.

Responsibilities

• Follow work policies, procedures, EHS protocols, and quality control inspection requirements during production
• Complete quality and compliance training on schedule; identify and report quality concerns with corrective action
• Operate within production processes and maintain documentation standards for non-conforming and rework requirements
• Comply with stop orders, concessions, ESD protocols, calibration, preventative maintenance, and material segregation procedures

Requirements

• High school diploma or GED equivalent
• Ability to read, follow work procedures, and understand GMP documentation requirements
• Strong communication skills with team leads, engineers, and supervisors
• Capacity to lift and carry up to 50 lbs regularly; occasionally more with assistance
• Ability to wear protective equipment and work in controlled environment conditions
• 2 years related manufacturing experience (preferred)
• Proficiency with MS Office applications including Teams, Outlook, Word, and Excel (preferred)