Process Engineer

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 commercialize 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 Engineer to join the Production Area of Diagnostic Instruments at Grifols SA, an industrial company engaged in research, development, and manufacturing of high-tech products for clinical diagnostics. Your responsibilities will include: Optimizing processes according to production requirements. Leading process improvement projects through implementation and training of the team on new processes. Evaluating existing equipment and processes to implement improvements in process performance and overall production ergonomics/safety. Developing action plans to achieve short- and long-term efficiency goals, selecting new production methods, designing production accessories, and defining methods to monitor efficiency. Focusing on continuous improvement. Classifying and leading Root Cause Analysis to resolve production incidents. Applying Lean and problem-solving methodologies to identify opportunities for cost reduction, delivery time reduction, inventory reduction, and quality improvement through defect reduction. Optimizing the production area layout and material flow. Implementing change controls and analyzing changes by performing necessary verifications, incorporating them into production processes via documentation and team training. Ensuring compliance with departmental GMP requirements. **Creating and reviewing production documents:** manufacturing guidelines, technology transfer reports, bills of materials, process descriptions, project reports. Creating and reviewing 3D assembly sequences to facilitate equipment assembly. Leading technical support for risk assessments, gap analyses, deviations, change controls, and CAPAs—including process impact assessment, root cause analysis, and identification of corrective actions. Investigating and determining root causes, establishing solutions, and following up on corrective actions to ensure their completion. Participating in cross-departmental projects. Collaborating with R\+D, Quality Assurance, Quality Control, Supply Chain, Global Manufacturing Engineering, Maintenance, and other departments to effectively transfer and maintain processes at facilities. Supporting technology transfer of internally and externally developed processes to manufacturing. Who you are To successfully perform this role, a candidate must be able to satisfactorily carry out the listed responsibilities. The requirements below are representative of the knowledge, skills, education, and/or abilities required. Role adaptations may be made to enable candidates with functional diversity to perform the job duties. You hold an engineering degree, specialized in Industrial Organization, Mechanical Engineering, Telecommunications, or a related field. Training or technical background in the healthcare sector is considered a plus. You have at least 3 years of experience performing similar tasks within a production environment. You have a high level of English proficiency, especially in writing and comprehension. You possess strong Office skills (especially Word and Excel) and experience with SAP or a similar ERP system. Basic programming knowledge and/or experience with Minitab are considered advantageous. You are communicative, highly team-oriented, and demonstrate leadership capability. You assume your responsibilities with accountability and autonomy. You are highly motivated to grow professionally, embrace new challenges, and remain open to continuous learning. 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, benefit from ongoing training, and integrate into a team of professionals where each individual’s contribution matters. Our commitment is to maintain a work environment that supports our employees’ professional development in a positive atmosphere. Grifols’ human capital is essential 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. **Flexible schedule:** Monday–Thursday: 7–10 a.m. and 4–7 p.m.; Friday: 8 a.m.–3 p.m. (with the same flexibility regarding start time). Benefits package **Employment contract:** Temporary Benefits package **Flexibility for U Program:** Occasional remote work **Location:** Parets del Vallès www.grifols.com \#LI\-Hybrid \#LI\-ER1 **Location:** SPAIN : Spain : Parets del Valles: \[\[cust\_building]] Learn more about Grifols