Process Control Assistant

Description

Job Summary: Process Control Assistant to supervise and verify production activities, ensuring processes comply with quality standards and regulatory requirements. Key Highlights: 1. Support supervision and verification of production activities. 2. Ensure product quality and traceability. 3. Be part of an international team in the healthcare sector. 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 Department 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 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, to guarantee product quality and traceability at each stage of the process. **Your Responsibilities Will Include** * Perform sampling according to the monitoring plan for critical facilities and services in the production plant: Water-for-injection and purified water distribution circuits, cleanrooms and aseptic areas, and compressed air circuits. * Conduct in-plant controls related to aseptic filling processes. * Perform process controls. * Review batch record documentation at all manufacturing stages. * Prepare materials for sampling. * Set up sampling equipment. * Enter results into the SAP quality management system. **Who You Are** To perform this job successfully, 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. Position adaptations may be made to enable individuals with functional diversity to perform the job duties. * You hold a high school diploma or a Medium-Level Vocational Training Certificate (CFGM) with experience. A Medium- or Higher-Level Vocational Training Certificate (CFGM/CFGS) in Chemistry or a related field is highly desirable. * You are available for weekly shift rotation (Morning/Afternoon and Night). * You have experience in Production departments 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 integrate into a team of professionals where each individual’s contribution matters. Our commitment is to maintain an environment that fosters employees’ professional development in a positive working atmosphere. Grifols’ human capital is key both in carrying out daily activities and in 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. **Working Hours:** Rotating schedule, Monday to Sunday**Professional Group:** 04**Benefits Package****Employment Contract:** Temporary**Location: Parets del Vallès** www.grifols.com Learn more about Grifols