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Engineering Manager
Do you have experience in both QA and GMP, and are you interested in utilizing your expertise to establish and run a new QA setup? If so, here’s your chance to make a significant impact in a leading and successful engineering company. We need you because the pharmaceutical industry is a strategically important growth area for ABB Denmark. We have an exciting pipeline of projects where we are developing and implementing automation solutions for pharmaceutical production. Working with pharma demands new and higher standards in documentation, processes, and more. We are therefore building a new QA function, and we already have a Lead QA professional whom you’ll work closely with. You will have the opportunity to use your skills across multiple areas. As mentioned, you will help creating the new ABB Pharma QA setup in Denmark, ensuring we work as smartly as possible. Simultaneously, you’ll handle classic QA tasks to ensure compliance with current regulations and customer requirements. On top of that, you’ll be instrumental in fostering a quality mindset among engineers. QA should be an integral part of every project, and for this reason you’ll be involved in projects from start to finish. Your path to success is largely rooted in your desire to create new solutions, including your ability to handle uncertainty and unpredictability. Alongside this, you should thrive with many points of contact. You’ll be the one to proactively reaching out and making things happen. Here, you’ll use your ability to drive the QA activities directly on the projects. Your responsibilities: • Contribute to developing a new QA setup with the right processes and tools. • Act as a QA specialist in engineering projects (pharma automation), participating from start to finish. • Approve and review test documentation and ensure the use of good documentation practices throughout the process. Additionally, preparation of deviations, reports, and quality plans • Ensure that documentation complies with current regulations and specific customer requirements. • Develop and maintain quality plans with the customers. • Guide and train both Danish and international automation engineers in GMP/GDocP. • Work in and provide support for TIMS (the customer’s verification and testing system).
Joining ABB opens the door to a world of opportunities. You’ll find that ABB is ready to invest in you and your development through relevant training and education. You can also look forward to working with competent colleagues in a positive and welcoming work environment. You are free to choose which of our Danish offices you’d like as your base – Kalundborg, Ballerup, or Middelfart. The job is highly flexible, with much of your work able to be performed remotely. However, you should be prepared to hold clarification meetings and train colleagues on-site in Kalundborg when needed. Please apply via our international career page. Use ”Denmark” as search criteria, then you will get a list with all Danish job openings. The deadline is February 7th – 2025 If you have questions, please feel free to contact Lars Schultz, Head of Pharma Engineering, at +45 2497 8635. For QA-specific questions, contact QA Lead Helle Mortensen at +45 7170 3282. We look forward to hearing from you. We value people from different backgrounds. Apply today for your next career step within ABB and visit www.abb.com to learn about the impact of our solutions across the globe. #MyABBStory
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