Key Skills

Job Description

As a Manufacturing Engineer you are responsible for giving support, improving and maintaining the production process within the Manufacturing Department Factory Best. This role is intended to update and validate all kind of equipment/process updates across the Factory Best organization. Job Responsibilities Writing work instructions, monitor/maintain devices and tooling, instruct employees, implement and maintain production processes. Preparation and introduction of product changes through Life Cycle Management and Modify Launched Design within the manufacturing processes. Execute Equipment, Software & Process Validation of the manufacturing processes. Defect On Arrival (DEFOA) /Missing On Arrival (MOA) Root cause analysis, creating and implementing structural solutions. Providing structural solutions by initiating amendments like problem reports (PR) and/or 8D forms (Problem Solving methodology) Leading escalations regarding production issues/complaints, if needed together with development and other stakeholders Minimum disturbances (max.Yield) within production in cooperation with teamleads, troubleshooters and development. Providing input for the Product Industrialization Engineer, to create a better way of working. After release for volume production the Manufacturing Engineer is accountable for improvements. Analysis of performance data with respect to products and processes (Six-sigma, Statistical Process Control Participates as an expert in audits. Give support to New Product Introductions. Give input and maintain the New Product Introductions project planning. Perform preparation activities on trial/prototype production within New Product Introduction-processes Defines and leads improvement projects for the assigned unit, to improve efficiency, product quality and test section (Green Belt) Requirments Bachelor's / Master's Degree in BioMedical Engineering, Industrial Engineering, Mechanical Engineering, Electronics Engineering, Sciences, Manufacturing Engineering or equivalent. Hands-on mentality, proficient in documentation and natural inclination for accuracy. Be independent, pro-active, and not afraid to take ownership, including relevant stakeholders’ management. A result & quality driven approach. Preferable Experience with SAP (MES) and Windchill > 2 years of experience within Manufacturing or Engineering within high tech industry Basic experience with OT (Operational Technology) and IT (Information Technology). Comprehension skills and ability to analyze and summarize. Experience with quality management and quality systems. Preferably experience in the medical industry (ISO 9001, 13485, FDA requirements, audits, FMEA, 8D, SPC, etc.). Human & communication skills. Communication with operators up to developers & management You will be employed by the Randstad and work on assignment at Philips.

Core Responsibilities

Maintain, validate, and improve manufacturing equipment and production processes, including product changes, new product introductions, and resolution of production defects and escalations. Analyze performance and quality data, lead improvement projects, support audits, and collaborate with production teams, development, and other stakeholders.

Requirements

A bachelor's or master's degree in biomedical, industrial, mechanical, electronics, manufacturing engineering, sciences, or an equivalent field is required. The role seeks more than two years of manufacturing or engineering experience in a high-tech industry, along with quality-system knowledge, analytical and communication skills, and preferably experience with SAP MES, Windchill, operational and information technology, and medical-industry standards.