Chinmayi Bhatt

Chinmayi is a chemical engineer specializing in strategy and process development in pharma and biotech. As Process Manager at Novo Nordisk, she develops and optimizes cross-functional processes to bring drug–device combination products to market faster, ensuring scalability, robustness, and regulatory compliance. Her background spans technical sales, medical device manufacturing, and enzymatic process innovation at Novozymes, with expertise in GMP, FDA, ISO, and MDR requirements. Holding an MSc from DTU and a BEng from NTU Singapore, Chinmayi combines technical depth with strong stakeholder engagement skills, thriving in multicultural, collaborative environments.

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Carsten Schaufuss-Feddersen

Carsten is a seasoned leader with over 20 years’ experience in medical devices and drug delivery, specializing in combination products from development through filing and commercialization. He has led device teams, built organizational capabilities, and integrated combination product development into broader product strategies. With expertise spanning design controls, risk management, human factors engineering, and regulatory compliance, Carsten bridges engineering, quality, and business needs. His career includes senior roles at CSL, Alnylam Pharmaceuticals, Amgen, and NNE, where he improved quality systems, guided regulatory submissions, and supported global manufacturing and supply chain operations.

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Anna-Kathrine Fevre

I have 16+ years of industrial and private practice experience within intellectual property rights from both biotech to Pharma companies. I deliver high quality, strategic and business oriented recommendations to peers, Executives and inventors. My professional expertise spans worldwide patent litigations, due diligence, freedom to operate analysis, and leadership including mentoring of younger associates and colleagues.
I have been involved in Global Regulatory Affairs tasks including strategic considerations and input to the business on high profiled projects, building bridges between regulatory and IP departments to ensure no gaps in exclusivity rights.

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Alicia Parra Acero

Alicia is a mathematics engineer specializing in AI, algorithms, and efficient programming. With experience across finance, pharma, software, biotech, and advanced imaging, she applies mathematical thinking to solve complex, real-world problems. Now a Staff Scientist at the Danish Cancer Institute, she works on computational image analysis and bioinformatics. Alicia holds an M.Sc. in Mathematical Modelling and Computation from DTU and a degree in Applied Mathematics from Universidad Complutense de Madrid.

She has 7+ years of experience in AI applications, data science and software development, within very different industries and company sizes. She has always been tight to the R&D departments, and my main motivation is to work in the biomedical field.

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Philipp Gruner

My career has revolved around developing, implementing, and applying cutting-edge microfluidic biotechnology that enables the development of next-generation biological solutions. I thrive on collaborating with others and navigate back and forth between the big picture and granular details. I am energized by assuming leadership roles and find great joy in helping the development of high performing teams.

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Habib Bahrami

Habib Bahrami, currently a Line Manager at Devote Consulting, boasts over 5 years of experience in the life sciences, medical devices, and healthcare sectors. A DTU-trained engineer with a MSc in Industrial Engineering and Management and a BSc in Biomedical Engineering, Habib excels in business process optimization to enhance organizational performance and patient quality of life. His previous roles include positions at Netcompany and Rigshospitalet, and he has substantial expertise in project management and GxP compliance.

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Bettina Grote

Bettina Grote is a Principal Software Process and Compliance Specialist at Oticon (Demant) with 16 years of experience in life science R&D, RA, and QA. She has expertise in design control, compliance, and documentation for medical devices, particularly in digital product R&D and SW platform processes. 

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Per Vaeggemose Nielsen

Per is a microbiologist and hygiene expert with decades of experience in food safety, biotech, and GMP. Today he runs his own consultancy, BioPres.dk, where he supports companies across the food and biotech industries with hygienic design, microbial risk management, and quality assurance. He has previously held global expert roles at CP Kelco and Chr. Hansen and has led research, training, and industry–university collaborations at DTU and IPU. Per is passionate about turning complex microbiological issues into practical solutions and enjoys mentoring others navigating careers in science and industry.

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Konstantinos Tsapralidis

I have 8 years of experience within the pharma industry from large companies and start ups in Denmark. My career has been in automation and IT areas in various pharma projects. At the moment i am working as QA in IT global projects for LeoPharma focusing in compliance of all IT systems.

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Ruba Zaki

I have 6+ years of experience within the healthcare industry. My career has revolved around ensuring that safe, effective and high-quality medical device solutions become available to patients worldwide in collaboration with different stakeholders. In the beginning of my career, my main focus was to investigate post-market data and now, I am focusing on design control within R&D.

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