Process Engineer Deviation Coordinator - Strängnäs

Job Description At Randstad Life Sciences, we are looking for someone who wants to work on an exciting assignment with one of our clients in Strängnäs. We are seeing an increased demand for technical expertise, and if you are interested in working with process support, deviation management, and continuous improvements in a production environment, you have come to the right place! As a consultant with Randstad Life Sciences, we are your employer, but you will have your daily workplace at one of our clients. Your consultant manager is always close at hand, both during and between assignments, to help you develop your career in the direction you dream of. As a consultant with us, you will receive a competitive salary, benefits, and collective agreement terms. We are attentive to your preferences regarding assignments and tasks, and with our broad client portfolio in Mälardalen, we will work together to tailor your continued career based on your skills, experience, and ambitions. At Randstad Life Sciences, we have a comprehensive understanding of what a consulting assignment entails, which means you have opportunities with us. You will be part of a larger consulting team within Life Sciences, giving you the chance to broaden your network and gain valuable experience from various workplaces. The assignment starts immediately and extends until after the summer. For the right person, there are excellent opportunities for extension or direct recruitment to the client. You will belong to the TIM – Technology Investigation Management group. This is the role for you if you want to specialize in the investigation craft itself. Your team is responsible for deviation investigations that span the entire flow: from raw materials and production to the quality organization. As a process engineer, you will act as the project manager for your deviations. You will lead cross-functional groups to identify root causes using Six Sigma tools and implement robust corrective actions (CAPA) that prevent the errors from occurring again. As a consultant with Randstad Life Sciences, you will have a secure employment with a collective agreement and benefits, while also having the chance to develop with one of the industry's most attractive employers. In this assignment, you will have a unique opportunity to combine work at a high-tech site with the flexibility of remote work. We welcome your application! Responsibilities • Lead and document deviation investigations within quality, production, and raw materials. • Drive troubleshooting and ensure that work adheres to set timelines. • Contribute to developing the site's quality culture and ensure cGMP compliance. • Participate in inspections and work on continuous improvements. Qualifications • University degree in a scientific field. • Good knowledge of and understanding of cGMP. • Fluent in Swedish and English, both spoken and written. • Strong communication skills. Preferred: • Experience in the pharmaceutical industry. • Previous experience leading deviation investigations. • Knowledge of Lean and Six Sigma. • Ability to handle uncertainties and drive processes forward independently. About the Company Randstad At Randstad, we know that everyone has a place in the labor market. With operations across the country and in all areas of expertise, we help people find jobs that feel right, where they can grow, develop, and reach their full potential. With nearly 600,000 employees in 38 countries, Randstad is a world leader in HR services, aiming to become the world's foremost and most appreciated partner in the labor market. By combining our passion for people with the power of today's technology, we help individuals and companies achieve their full potential. We call it Human Forward.