Process Control Assistant – Conditioning

Description

Job Summary: We are seeking a Process Control Assistant for the Conditioning area to ensure the proper execution and monitoring of operations, complying with quality, safety, and productivity standards. Key Highlights: 1. Improve global health and well-being through an international company. 2. Join a team that values diversity and professional development. 3. Contribute to the production of therapeutic plasma proteins. **table.MiTabla { max\-width:** 1020px;!important Would you like to join an international team working to improve the future of healthcare? Do you want to contribute to improving the lives of millions of people? Grifols is a global healthcare company that has been enhancing people’s health and well-being worldwide since 1909. We are leaders in hemoderived medicines and transfusion medicine, and we develop, manufacture, and market innovative medicines, solutions, and services in over 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 strengthen our company. We are looking to hire a Process Control Assistant for the Conditioning area within the Biopharma Division of the Grifols Institute — a company specialized in the research, development, and production of purified plasma proteins with therapeutic properties obtained from human plasma fractionation. Role Mission Ensure the correct execution and monitoring of operations in the conditioning area, guaranteeing compliance with quality, safety, and productivity standards; verify continuous workflow, record production data, detect deviations, and support the implementation of improvements. Your Responsibilities Will Include You will perform sampling operations, including visual inspection and correct secondary conditioning of units. You will perform sampling of conditioning materials. You will segregate and review batch release units, as well as reference/retention units. You will prepare and monitor work schedules and forecasts based on existing production programs and controls. Who You Are To successfully perform this role, a candidate must be able to carry out the responsibilities satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or abilities required. Role adaptations may be made to enable persons with functional diversity to perform the job tasks. You hold a Higher Vocational Training Certificate (CFGS) in Chemistry, Pharmacy, Quality Control Analysis, or a related field. A pharmaceutical specialization is preferred. You are available to work the afternoon shift. 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 standard operating procedures such as GMP and PNT (Highly desirable). 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 grow professionally, access continuous training, and become part of a team of professionals where each individual contribution matters. Our commitment is to maintain a work environment that supports our employees’ professional development in a positive atmosphere. Grifols’ human capital is key both to carrying out daily 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. **Working Hours:** Afternoon shift, Monday to Friday **Employment Contract:** Permanent Benefits Package **Location:** Parets del Vallès. Learn more about Grifols