Analytical Quality Management Assistant – Afternoon Shift

Description

**table.MiTabla { max\-width:** 1020px;!important Would you like to join an international team working to improve the future of the healthcare sector? 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. Help us lead one of the world’s largest pharmaceutical companies. We are a global leader in plasma-derived medicines, present in over 100 countries, with a growing global team of more than 20\.000 people. That’s why we need Analytical Quality Management Assistants for our subsidiaries — like you. Role Mission You will perform physical-chemical and microbiological analytical controls on raw materials, materials, and manufactured products, ensuring compliance with quality standards, Good Manufacturing Practices (GMP), and established procedures. You will also contribute to ensuring the reliability of analytical results and support product release and continuous process improvement, collaborating with the various teams involved in manufacturing and quality assurance. Your Responsibilities Will Include You will conduct physical-chemical assays on manufactured products (finished product, process validations, stability studies, analytical method validations). You will perform endotoxin testing, microbial enumeration, and sterility testing on manufactured products (finished product, process validations, stability studies, analytical method validations). You will carry out analytical controls on raw materials and other materials related to manufactured products. You will collaborate in the investigation of incidents and complaints. Who You Are To successfully perform this role, a person must be able to satisfactorily fulfill the responsibilities listed. The requirements below are representative of the knowledge, skills, education, and/or abilities required. Job adaptations may be made to enable individuals with functional diversity to perform the tasks associated with this position. You hold a Medium or Higher Vocational Training Certificate (CFGM/CFGS) in Quality Analysis and Control or Pharmaceutical, Biotechnological, and/or related Product Manufacturing. You have at least 2 years of experience in quality control. You possess knowledge and/or experience in the quality field and the pharmaceutical industry, such as GMP and PNT (Highly Valuable). English level B2 (Valuable). Experience using MS Office at user level; SAP experience (Valuable). You are proactive and solution-oriented, and enjoy working in dynamic environments and with diverse teams. 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 contribution matters. Our commitment is to maintain an environment that fosters our employees’ professional development within a positive workplace 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 Afternoon Schedule:** Monday to Friday, 2:00 PM – 10:15 PM Benefits Package **Employment Contract:** Permanent **Location:** Parets del Vallès www.grifols.com Learn more about Grifols