Work Flexibility: Onsite

What you will do

Support Manufacturing/Operations for the Surgical Stryker Sustainability Solutions Business during Transfer and Post-Launch activities, concentrating on a specific project to ensure business stability.

Responsibilities for this project role include:

Evaluating manufacturing outcomes and implementing continuous improvements and cost efficiencies, supporting New Product Introductions (NPI) and new equipment/process introductions, increasing capacity, reducing scrap, improving yield, enhancing safety, monitoring existing processes, and identifying and implementing process improvements within a regulated medical device reprocessing environment.Apply Statistical, Lean, GMP, and Six Sigma methodologies to support and improve existing processes, ensuring they align with the project’s scope and objectives.Manage the effective transfer of new products, design changes, or line-extended devices to production, focusing on Transfer and Post-Launch activities.Foster a culture of continuous improvement by collaborating with cross-functional teams and providing project-specific support across all functional areas.Conduct Failure Analyses (FAs) and implement enhancements to improve the functionality, performance, and reliability of medical devices.Optimize manufacturing processes by implementing process improvements, reducing scrap rates, enhancing machining operations, and ensuring compliance with safety standards.Develop and execute technical protocols, generate comprehensive reports documenting project milestones, and implement clear operating procedures, including standard work and visual work instructions.Train production staff on new product launches and design changes, ensuring smooth transitions and alignment with project requirements.Gain and apply in-depth knowledge of FDA/ISO standards, including Design Control, to ensure compliance and support the successful execution of medical device projects.

What you need

B.S. in Engineering (Industrial, Mechanical, Electrical or related).Minimum 2 years of experience as Manufacturing Engineer in a highly regulated industry, preferably in a Medical Devices company.Experience with development of protocols for process validation.Knowledge of One PLM, Valgenesis and SAP systems is a plus.Knowledge of AutoCAD is desirable.Basic computer skills (word processing, spreadsheets, database).Conversational English.Problem solving skills.Availability to work on a 14 months contract.

Travel Percentage: 20%