Hybrid Engineer II Manufacturing Packaging - Exton, PA (United States) at Our Company
Our Company · Exton, United States Of America · Hybrid
- Professional
- Office in Exton
Engineer II Manufacturing Packaging
Exton, PA
The Engineer II Manufacturing Packaging will provide technical support, packaging design, and processing expertise towards the final stage development, scale up, and commercialization for new and existing product lines. This role will assist Research, Commercialization, & Quality Engineers tasked with developing and/or improving current and future Biomedical processes related to challenges surrounding packaging. The engineer will participate on project teams within the PMP/project management process.
Key Responsiblities:
- Independently identify, evaluate, and assist the optimization of process variables required for maximizing packaging/process performance at full production scale.
- Conduct evaluations of final packaging specifications by prototyping packaging/processes and performing experiments; from lab to production scale.
- Execute the evaluation of scale up options, selections, and implementation through sub projects, providing project updates and input for the next phase.
- Execute designed studies to demonstrate packaging/process performance at prototype, lab/pilot scale, and full production scale
- Interfacing with Operations to address plant layout, resources, and start up milestones
- Develop all necessary documentation to support improved packaging in manufacturing
We Bring:
- A competitive compensation package, with comprehensive health and welfare benefits
- A place to grow and develop
- A company that is purpose-led and performance-driven in a corporate culture that values people and planet
- The opportunity to work on growing brands and build on a strong foundation
- The chance to make improvements and make an impact on the business
You Bring:
- Bachelor’s degree in Engineering – Biomedical, Mechanical, Electrical, Chemical, Materials, or related field
- A minimum of 2-6 years of experience in Medical Device or related industry
- Experience in equipment and process validation (IQ, OQ, and PQ) to transfer new processes and equipment into manufacturing.
- Experience in Root Cause analysis and incident investigation skills as well as problem solving.
- Technical knowledge and experience in managing multiple projects / tasks with minimal supervision.
