Within the Pharma Process area and as part of the new structure dedicated to the Aseptic Project, the CNC Operator will join one of the production phases during the project, actively participating in it and in the associated processes. The CNC Class includes the production processes of Inspection, Device Assembly, and Packaging. During the project phase, it is essential that the operator collaborates in process development, creation of area procedures, and support throughout the equipment and process validation cycle. Below are the main functions/responsibilities dedicated to the project phase and the transition into routine production. **Functions and responsibilities** **Project:** * Participate in the development of area processes along with all necessary documentation (manuals, SOPs, etc.), according to current safety, quality, and production regulations. * Support the development of the Inspection, Device Assembly and/or Packaging process for Aseptics as applicable. * Actively participate in the entire validation cycle of equipment and processes. * Operate area equipment during the validation cycle. * Support the technical team leading the area's projects and identify applicable improvements for the section. * Participate in the implementation of process-related documentation. * Provide support to other process areas when required. * Material handling within CNC areas. **Routine:** * Perform all necessary operations to carry out the inspection, Device Assembly and/or Packaging process (machine operation, sampling, IPCs, electronic guides, interventions, etc.) safely and sustainably in compliance with GMP standards to ensure product quality. * Perform necessary operations on auxiliary equipment in the area. * Material handling within CNC areas. * Provide support to other aseptic process areas when required. **Requirements** * Higher Technician or equivalent qualification in Pharmaceutical Product Manufacturing (FP/CFGM/S) highly valued. * Minimum 3 years of experience in the pharmaceutical industry. * Solid knowledge of pharmaceutical regulations GMP and FDA. * Experience in inspection, Device Assembly and/or Packaging of sterile or aseptic products highly valued. * Methodical, responsible person with concentration ability and decision-making skills. * Excellent analytical and problem-solving skills, organization and prioritization, as well as teamwork and proactivity. * Availability to work shifts (2-shift or 3-shift depending on project phase). \#IamBoehringerIngelheim because… We are continuously working to design the best possible experience for you. Here are some examples of how we’ll take care of you: * Reserved parking * Lockers * Life and accident insurance * Health care * Special offers portal for employees * School assistance * Christmas gift basket If you've read this far, what are you waiting for? We want to know more about you!