Onsite Serum Manufacturing Associate

Cytiva; Logan (UT); On-site; USD 42,000 - 68,000; Full time

Job summary

Cytiva in Logan, Utah, is seeking an on-site Manufacturing Associate for the Serum - Large Volume Liquid Volume Manufacturing department. The role requires following work policies, GMPs, and quality controls to ensure product conformance.

You will train in quality/compliance and assist with production processes and documentation practices. The position emphasizes attention to detail, teamwork with engineers and supervisors, and safe handling of materials in a cleanroom environment.

Qualifications

• High School Diploma/GED or local equivalent.
• Ability to work well and communicate with team lead, engineers, supervisors, and managers to improve quality and process efficiency.

Responsibilities

• Read and follow work policies and procedures, EHS, Quality control inspections along with schematics or verbal instructions regarding duties to be performed. GMPs and Good documentation skills.
• Complete all planned Quality & Compliance training within the defined deadlines. Identify and report any quality or compliance concerns and take corrective action as required.
• Knowledge and understanding of production process, work instructions, documentation configuration control, non-conforming and rework documentation requirements and operate within them to ensure the product conforms to its specification; aware of Stop Order, Concessions, ESD, Calibration, Preventative Maintenance, Material Identification & Segregation, and Good Documentation Practices.

Skills

Team communication

Quality control

Documentation practices

GMP knowledge

Education

High School Diploma/GED

Tools

MS Office

Job description

Cytiva in Logan, Utah, is seeking an on-site Manufacturing Associate for the Serum - Large Volume Liquid Volume Manufacturing department. The role requires following work policies, GMPs, and quality controls to ensure product conformance.

You will train in quality/compliance and assist with production processes and documentation practices. The position emphasizes attention to detail, teamwork with engineers and supervisors, and safe handling of materials in a cleanroom environment.