Job Summary: Support the supervision and verification of production activities, ensuring that processes are carried out in accordance with Standard Operating Procedures (SOPs), quality standards, Good Manufacturing Practices (GMP), and regulatory requirements. Key Highlights: 1. Be part of an international team improving the future of healthcare 2. Professional development and continuous training 3. Inclusive environment with equal opportunities Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. **We believe diversity adds value to our business, our teams and our culture. We are committed to equal opportunities and our mission is to provide an inclusive environment where differences contribute to our company.** We are seeking a **Process Control Assistant** for the Technical Area at **Instituto Grifols SA**, a company specialized in the research, development and production of purified plasma proteins with therapeutic properties obtained from human plasma fractionation. **Role Mission** Support the supervision and verification of production activities, ensuring that processes are carried out in accordance with Standard Operating Procedures (SOPs), quality standards, Good Manufacturing Practices (GMP) and regulatory requirements, in order to ensure product quality and traceability at each stage of the process. **Your responsibilities will include** * Performing sampling according to the monitoring plan for critical facilities and services at the production plant: Water for Injection and Purified Water distribution circuits, cleanrooms and aseptic areas, and compressed air circuits. * Conducting on-site controls related to aseptic filling processes. * Performing process controls. * Reviewing batch record documentation at all manufacturing stages. * Preparing materials for sampling. * Setting up sampling equipment. * Entering results into the SAP quality management system. **Who You Are** To successfully perform this role, a person must be able to carry out the responsibilities satisfactorily. The requirements listed below are representative of the knowledge, skills, education and/or abilities required. Job accommodations may be made to enable individuals with functional diversity to perform the essential functions of the position. * You hold a High School Diploma or Vocational Training Certificate (CFGM) with experience. A CFGM/CFGS in Chemistry or related field will be highly valued. * You are available for weekly shift rotation (Morning/Afternoon and Night). * You have experience in Production areas within the Chemical/Pharmaceutical sector, with knowledge of GMP regulations. * You possess user-level proficiency in MS Office. * Knowledge of work standards such as GMP, PNT (Highly Valuable). * You are proactive, solution-oriented and eager to learn. **What We Offer** Joining Grifols means the opportunity to work in an internationally oriented environment that promotes equal opportunities. It means the opportunity to develop professionally, access continuous training and become part of a team of professionals where each individual contribution matters. Our commitment is to maintain an environment that fosters professional development for our employees in a positive working atmosphere. Grifols’ human capital is key both to carrying out our activities and to the company’s expansion process. If you are interested in growing with us and your profile matches this professional opportunity, please send us your CV.**On-site schedule: Rotating (Morning/Afternoon and Night)****Benefits package****Employment contract: Permanent.** **Location:** Parets del Vallès www.grifols.com Learn more about Grifols