Process Control Assistant – Conditioning

Description

**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 plasma-derived 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 seeking a Process Control Assistant for the Conditioning area within Grifols Institute’s Biopharma Division — a company specialized in researching, developing, and manufacturing purified plasma proteins with therapeutic properties obtained through 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 verification of 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 satisfactorily fulfill the responsibilities outlined above. 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 carry out 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 highly valued. 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 (Preferred Notation for Technical Procedures) is 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 integrate into a team of professionals where each individual’s contribution matters. Our commitment is to maintain an environment that supports our employees’ professional development in a positive workplace atmosphere. Grifols’ human capital is essential both in carrying out daily activities and in the company’s expansion process. We believe in diverse talent and aim to remove any barriers that could hinder your participation. If you require any accommodations during our selection process, please do not hesitate to let us know when applying. We are here to help. **Schedule:** Fixed afternoon shift, Monday to Friday, from 14:00 to 22:00\. **Employment Contract:** Temporary. Benefits Package **Location:** Parets del Vallès. Learn more about Grifols