Aseptic Media Prep Specialist – GMP Biopharma

Boehringer Ingelheim; Saint Joseph (MO); Presencial; USD 45 000 - 65 000; Tempo integral

Resumo da oferta

Boehringer Ingelheim is seeking an Aseptic Media Prep LG4 to support manufacturing of high-quality biological products in a GMP environment. You will perform records management, operate and calibrate equipment, and assist in training staff to maintain aseptic techniques.

The role emphasizes collaboration, adherence to regulatory standards, and continuous process improvement within a busy production facility in Missouri. Applicants must be eligible to work in the United States.

Qualificações

• High school diploma or equivalent.
• Good verbal and written communication skills and ability to train others.
• Ability to use basic logic to identify and solve problems.
• Demonstrated understanding of GMP/Documentation practices.

Responsabilidades

• Prepares, reviews and audits for completion and accuracy all assigned records, calibration, and documentation in assigned area to ensure regulatory compliance.
• Reads and follows schedules, procedures, and documents.
• Assists in training other employees in an area of responsibility as assigned.
• Assists staff in developing new procedures and methods or improving old ones.
• Uses and understands computer assisted data entry including MES, SAP, scanners, printers, scales, and other integrated equipment.
• Assists in the transfer of new products, new test methods, new production processes, and new technology.

Conhecimentos

Verbal and written communication

Train others

Problem solving

Teamwork

Attention to detail

Formação académica

High school diploma or equivalent

Ferramentas

SAP

MES

Scanners

pH meters

OIM/OSMometer

Descrição da oferta de emprego

Boehringer Ingelheim is seeking an Aseptic Media Prep LG4 to support manufacturing of high-quality biological products in a GMP environment. You will perform records management, operate and calibrate equipment, and assist in training staff to maintain aseptic techniques.

The role emphasizes collaboration, adherence to regulatory standards, and continuous process improvement within a busy production facility in Missouri. Applicants must be eligible to work in the United States.