**Job Title**: Labeling Engineer 2**Job Overview**Bring your passion and energy into a growing department dedicated to the quality output of product labeling and packaging for Sleep & Respiratory Care(SCR) devices in accordance with GMP's, FDA Regulations, EUMDR, ISO Requirements and Standard Company Operating Procedures**Responsibilities**- Provides first line engineering support to ensure production- Initiates production escalations, executes problem solving related toManufacturing processes, tools and equipment- Prepares, plans and executes Capex projects for repeat equipment- Obtains and installs repeat equipment at site- Implements LCM design changes in their site- Accountable for integrity of Master data- Identifies and executes improvements in manufacturing processes, tools andequipment. This for quality and efficiency improvements- Applies lean manufacturing principles- Supports and applies new technologies in factories- Employs equipment, practices, and procedures which promote a healthy,safe, and secure work environment- Executes the processes and standards with embedded quality into the way ofworking including adherence to compliance with safety, Cost regulatory- andenvironmental requirements as well as local laws, Philips General Businessprinciples and other policies - Defines, executes and controls validation activities in LCM.- Performs technical analysis and participates in feasibility studies.- Driving current state and future state roadmap factory/VSM.- Operations involvement in PDLM by providing input into manufacturingrequirements and gate reviews- Responsible for the performance of processes, tools and equipment afterproject hand-over is completed (catching)- Provides expert support in outsourced product industrialization and changeImplementation**Requirements**:- Bachelor's Degree or equivalent experience- Intermediate/Advanced English level- 4 to 5 years of Medical device - Label graphic design experience- Understanding of labeling requirements & labeling standards like ISO 15223- Knowledge of Regulatory standards (FDA, EU** MDR**, Japan, Canada, ISO standards) is preferred- Create / Update labels, including label template creation- Experience in redlining labels as per the requirements- Experience in labeling software's - Enlabel, Leankit, Xiam, Illustrator, Loftware Spectrum- Label proofreading experience- Experience in releasing labels in PLM systems like Windchill- Project management experience is preferred- ** Shift: Administrative****About Philips**We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.- Learn more about our business.- Discover our rich and exciting history.- Learn more about our purpose.LI-PH1
