3D Technologies Co-op: QC & Process Innovation

MSD; Pennsylvania; Presencial; USD 40.000 - 111.000; Jornada completa

Descripción de la vacante

MSD is seeking a 3D Technologies Coop in the Future Talent Program to support QC, equipment qualification, and process improvements across 3D printing and analytical workflows. You will qualify equipment, analyze defects, document issues, and collaborate with multiple departments to expand pharmaceutical manufacturing capabilities.

The role emphasizes hands-on post-processing, data analysis, and strong documentation skills, with a 4–6 month full-time commitment starting Apr 2027 and onsite work

Formación

• Currently pursuing a degree in a STEM field and returning to university after the co-op.
• Available for full-time employment for 4–6 months Apr 2027 – Sep 2027.
• Role primarily onsite with attendance 4–5 days per week.

Responsabilidades

• Qualify new printers or other equipment into service and outline processing conditions to meet minimum quality controls (e.g. FDM, SLA, injection molding).
• Identify root causes of print failures across a fleet and document equipment failures to improve QC checks and training of automated systems.
• Identify workflows in lab Dev & Ops and 3D printing production for improvement opportunities; conduct research to expand capabilities (3DP for injection molding, tablets/pills, wetted path components).
• Utilize material characterization and imaging equipment (e.g. micro-CT, hardness testing, tensile testing) to understand defects and improve processes.

Conocimientos

Assembly processes

Data analysis

Data visualization

Data wrangling

Defect analysis

Chemical engineering

Data security

Educación

Mechanical Engineering

Materials Engineering

Chemical Engineering

Electrical Engineering

Descripción del empleo

MSD is seeking a 3D Technologies Coop in the Future Talent Program to support QC, equipment qualification, and process improvements across 3D printing and analytical workflows. You will qualify equipment, analyze defects, document issues, and collaborate with multiple departments to expand pharmaceutical manufacturing capabilities.

The role emphasizes hands-on post-processing, data analysis, and strong documentation skills, with a 4–6 month full-time commitment starting Apr 2027 and onsite work