Nina-Marie Højgaard Dovmark

Senior Quality Engineering Consultant at PharmEng Technology

Nina-Marie Højgaard Dovmark has a diverse work experience. Nina-Marie currently works as a Senior Quality Engineering Consultant at PharmEng Technology since June 2022. Prior to this, they worked at NNE as a Consultant from December 2016 to August 2020. Nina-Marie also gained experience as a Student Assistant at Novo Nordisk A/S, Environmental Monitoring from February 2014 to July 2016. Additionally, they worked as a Student Assistant at DTU Mechanical Engineering from September 2009 to February 2016. Nina-Marie'searly work experience includes a role as a Telemarketing Associate at Berlingske Media from September 2009 to February 2010.

Nina-Marie Højgaard Dovmark's education history begins in 2010 when they enrolled at the Technical University of Denmark. Nina-Marie pursued a Bachelor's Degree in Human Life Science Engineering, also known as Teknisk Biomedicin in Danish. Nina-Marie successfully completed their undergraduate studies in 2014.

In 2012, Nina-Marie was granted the opportunity to study abroad at UC San Diego for a year, although their field of study during this time is unspecified.

After completing their Bachelor's Degree, they decided to further enhance their knowledge and skills by pursuing a Master of Science in Engineering (M.Sc.Eng.) in the field of Biotechnology at DTU - Technical University of Denmark. Nina-Marie enrolled in 2014 and completed their postgraduate studies in 2016.

During their educational journey, Nina-Marie also attended a General English Course at British Study Centres in 2010, where they achieved an advanced level of proficiency in the English language.

Overall, Nina-Marie's educational background showcases their dedication to the field of biotechnology, as they have obtained both a bachelor's and a master's degree in the subject.

Location

Copenhagen, Denmark

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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).


Headquarters

Toronto, Canada

Employees

201-500

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