Senior Aseptic Filling Process Engineer

Takeda Pharmaceutical Co.; Round Lake (IL); Presencial; USD 90.000 - 141.000; Jornada completa

Descripción de la vacante

Takeda Pharmaceutical Co. is seeking a Process Engineer to support aseptic filling operations, partnering with Manufacturing, Quality, Validation and Reliability Engineering. The role focuses on precision web handling, sealing, volumetric dosing, and process optimization to improve yields and reduce downtime.

You will lead technical change requests, investigations, CAPA and capital-project input. Collaboration across QA, Regulatory, and site teams is essential.

Formación

• Bachelor’s or advanced degree in science, engineering or related field.
• 3+ years of related experience in process engineering or manufacturing.
• Ability to lead projects and coordinate contractors.
• Strong verbal and written communication, including senior management presentations.
• Proficient with MS Word, Excel and PowerPoint.

Responsabilidades

• Identify and implement projects to improve quality or efficiency of filling operations.
• Act as a technical leader across Quality, Manufacturing, suppliers, and relations.
• Lead the technical aspects of change requests, CAPA, and continuous improvement programs.
• Lead troubleshooting to resolve equipment issues and reduce downtime.
• Introduce new filling equipment and technologies.
• Author and execute user requirements, technical and validation protocols.

Conocimientos

Interpersonal skills

Project leadership

Technical troubleshooting

Documentation

MS Office

Educación

Bachelor’s degree in Science or Engineering

Mechanical Engineering degree

Herramientas

Microsoft Project

AutoCAD

SolidWorks

Descripción del empleo

Takeda Pharmaceutical Co. is seeking a Process Engineer to support aseptic filling operations, partnering with Manufacturing, Quality, Validation and Reliability Engineering. The role focuses on precision web handling, sealing, volumetric dosing, and process optimization to improve yields and reduce downtime.

You will lead technical change requests, investigations, CAPA and capital-project input. Collaboration across QA, Regulatory, and site teams is essential.