Morten Munk Email & Phone Number

Helsingør, Dk

Billingham, Gb

Supporting FDB’s clients and partners in developing and manufacturing biopharmaceuticals at FDB globally.

Hørsholm, Dk, Dk

Part of the team to develop and commercialize a microbiome based pharmaceutical treatment

Virum, Capital Region, Dk

NNE is an international company, headquartered in Denmark, specialised in pharma engineering. With more than 80 years of experience, we are passionate about our services to the pharma and biotech industries. NNE helps pharmaceutical companies bring products to market by providing flexible, compliant and future-proof solutions. We have close to 2,000 professionals delivering global knowledge and best practices, all dedicated to supporting our customers globally and on local sites.Role: Biopharmaceutical specialist supporting NNEResponsibilities:- Supporting NNE's increased visibility and status as first choice for compliant pharmaceutical engineering- Presenting on technical and quality related subjects at international conferences- Writing technical and quality oriented articles and technical reports- Chairing and organizing international conferences, ensuring NNE Pharmaplan presents and influence in international organizations such as PDA and ISPE, and building valuable network within the pharmaceutical consultancy and especially regulatory community.

Bothell, Wa, Us

CMC Biologics was founded in 2001 in order to provide faster and more effective solutions to the bio-pharmaceutical industry’s growing need for outsourced development and manufacturing resources. To meet the needs of a growing base of customers around the world, they expanded into the U.S. through acquisition of the process development laboratories and manufacturing facility from ICOS Corporation, re-branding the global organization to CMC Biologics, Inc. in 2008. Today, CMC Biologics consist of more than 500 dedicated employees who are committed to provide great solutions for more than 100 customers on five continents.Position: Global Key Account Manager for CMC Biologics' strategic and key collaboration partners.Responsibilities:- Technical and Business Development Subject Matter Expert- Negotiation of double digits million Euro commercial supply agreements- Business Development in Scandinavia, Asia and selected other countries- Supporting CMC Biologics' increased visibility and status as technical competent - Quality oriented commercial CMO- Presentation of technical and quality related subjects at international conferences- Writing technical and quality oriented articles and technical reports- Chairing and organizing international conferences, ensuring CMC Biologics presents and influence in international organizations such as PDA and ISPE, and building valuable network within the pharmaceutical consultancy and especially regulatory community

Bothell, Wa, Us

CMC Biologics remains vigilant in meeting customers’ growing demand for scalable biologics production. Its continued investment in technological advances, innovative facility designs and rapid facility expansions benefits customers and drives growth. CMC Biologics is dedicated to its customers’ focus to bring effective, safe medicines to patients quickly – improving lives.Responsibilities:- Line responsible for Downstream Operations. 5 to 15 persons- Development of downstream processes for production of API’s- Responsible for downstream production of toxicological and clinical API batches - Process specific user demand specifications for production facilities - Downstream production facility- Project management for customer projects

Bothell, Wa, Us

CMC Biologics is a global Contract Manufacturing Organization with three bio-manufacturing facilities in Europe and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologic manufacturing services, from DNA to active pharmaceutical ingredient. The company’s team and approach are tailored to each of its client’s needs, whether it is turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services. Task: I was re-located to work out of CMC's site in Bothell - Seattle, Washington for 15 months. Results: I moved back to Denmark, after a successful stay in Seattle, where the initial task was to establish a strong US based BD team, which was followed by heading CMC’s efforts to established a more global presence of CMC Biologics, with special focus on Japan and the rest of the Asian region. This work is now continued with Copenhagen as the home base.

Bethesda, Maryland, Us

PDA offers several valuable resources, including Technical Reports. I am pleased to have been part of the development of numerous TR’s, including being co-chair, together with Bob Repetto (Pfizer) for the upcoming TR on Single Use Systems, together with an excellent team of experts from the PDA network. As a PDA board member, I will do my best to continue the proud traditions of PDA and the organization’s constant strive to improve and expand its offering to members.I am honored to be nominated to the PDA Board of Directors. From the past 10 years of my involvement with PDA, I have developed a strong network and knowledge-base from my membership. I’m dedicated to be driving the PDA mission of defining issues scientifically, deriving technically sound and practical solutions, and at the same time always meeting the highest quality standards. Responsibilities:- Organizing and presenting at several successful conferences, featuring this emerging technology- Organizing high quality conferences- Meetings and training events, are also valuable and educational outcomes of PDA’s activities

Bagsværd, Dk

Novo Nordisk is a global healthcare company with more than 90 years of innovation and leadership in diabetes care. This heritage has given us experience and capabilities that also enable us to help people defeat other serious chronic conditions: haemophilia, growth disorders and obesity.Headquartered in Denmark, Novo Nordisk employs approximately 41,000 people in 75 countries and markets its products in more than 180 countries.Responsibilities:- Insulin process development- CMC project management of two major insulin development projects- Internal expert on process development- Facility design, validation and regulatory issues- Technology transfer to research development, production and engineering departments - Evaluation of new process technology, patent and production strategies- Collaboration agreements with vendors and other partners

Engineer’S Degree, Chemical Engineering

High School Student