Job Responsibilities
La siguiente información ofrece un resumen de las habilidades, cualidades y cualificaciones necesarias para este puesto.
Lead packaging process development from concept through market launch to meet business objectives, applying Lean Manufacturing and Six Sigma methodologies to optimize new and existing processes.
Partner with R&D teams to ensure product manufacturability, using Design for Manufacturing and Assembly methodologies to identify potential failure modes early and achieve optimal production cost and performance.
Contribute as part of Global Integrated Engineering teams, collaborating with multi-functional engineering groups and supporting the development of machine and process specifications.
Drive cost reduction and process improvement initiatives, leading hands‑on resolution of packaging issues at manufacturing sites, including shop‑floor troubleshooting, root‑cause analysis, and implementation of sustainable corrective actions.
Plan and complete process development trials and DOEs for packaging, and create, maintain, and document process requirements and manufacturing know‑how.
Lead activities at the Packaging Development Laboratory, planning and delivering laboratory testing to support packaging design, process development, and manufacturing readiness.
Evaluate and assess new technologies, intellectual property, products, and industry trends with the potential to impact global packaging processes, capabilities, and business performance.
Travel Requirements
Up to 50% travel to assist with global packaging process development, industrialization, and resolving manufacturing issues.
Qualifications
Bachelor’s or Master’s degree in Engineering (Biomedical, Mechanical, Manufacturing, Materials, or related field)
5+ years of experience in process engineering within the medical device, pharmaceutical, or regulated manufacturing environment (e.g., food)
Proven experience in packaging process development and test equipment
Demonstrated technical leadership, strong engineering fundamentals, and clear technical communication and documentation skills
Proficiency in CAD tools and statistical analysis software (e.g., Minitab)
Proficient English (C1 level or equivalent)
Preferred Skills
Knowledge of medical device processes and design controls
Strong background in Lean Manufacturing, Six Sigma, and DFMA methodologies
Hands‑on experience with process validation, Design of Experiments (DOE), and equipment/process specification development
Strong root cause analysis and structured problem solving in plant‑floor environments
Salary Range
EUR 45,000 - 55,000 per year.
Equal Opportunity Employer
Becton, Dickinson, and Company is an Equal Opportunity Employer. xpzdshu We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
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