PharmEng Technology
Dorte Siv Johnsen has a diverse work experience spanning several companies and roles. Dorte Siv'smost recent position was as a Quality Engineer at PharmEng Technology, starting in April 2023. Prior to that, they worked as a GMP Compliance Consultant at Eltronic A/S from July 2022 to February 2023. Dorte Siv also served as a Quality Support at Meditec A/S from June 2021 to October 2021. Before that, they worked as a Lean Manufacturing Engineer at Hero Gears A/S from November 2020 to June 2021.
Dorte also has a significant tenure at Novo Nordisk, where they held various roles. Dorte Siv worked as a Quality Coordinator from June 2015 to May 2020 and as a Supporter from October 2012 to May 2015. Additionally, they worked as an Afgangsprojektstuderende at Topsil Semiconductor Materials A/S from January 2011 to June 2011, where they successfully completed a project to reduce variation in the weight of 6" mono-crystals.
Dorte gained valuable experience during their Ingeniørpraktik at Jensen Denmark A/S from February 2010 to July 2010. Dorte Siv worked on projects related to optimizing time management, improving production efficiency, and reducing delivery time between two factories.
Dorte Siv'scareer began as an Afdelingsleder at SuperBest from February 2006 to January 2007.
Dorte Siv Johnsen completed a Bachelor of Science (B.S.) degree in Production at Copenhagen University College of Engineering from 2008 to 2011.
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PharmEng Technology
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PharmEng Technology is a leading global provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes. Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique needs and challenges. At PharmEng Technology, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives and develop customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs. As a trusted partner to some of the world's largest pharmaceutical companies, we have a proven track record of success in delivering high-quality technical services and solutions that drive operational efficiency, reduce costs, and enhance overall performance. We are dedicated to helping our clients succeed in an ever-evolving and highly competitive industry. At PharmEng Technology, we are passionate about what we do, and we are committed to delivering excellence in everything we do. Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).