Production Validation Specialist

We are looking for a highly skilled Safety Surveillance Specialist to join our team at Novo Nordisk A/S.About the TeamThe Obesity team handles projects within obesity and other indications from development to post-marketing. As a Safety Surveillance Specialist, you will work in collaboration with other colleagues in the team to perform surveillance...

Job DescriptionFerrosan Medical Devices A/S is a leading provider of medical devices used in surgical care. We are seeking an experienced Medical Device Quality Assurance Specialist to join our team.About the RoleThe successful candidate will be responsible for ensuring the highest quality of our medical devices, working closely with various teams to ensure...

About the DepartmentThe RA CMC Synthetics & Cell Technologies department is a key player in the development of new medicines at Novo Nordisk. As a CMC Regulatory Specialist, you will join a team of experts who are passionate about delivering high-quality products that meet regulatory requirements.Our team is responsible for driving the regulatory affairs CMC...

Technical Support & Utilities Department Overview:The Technical Support & Utilities department at Ferrosan Medical Devices A/S is responsible for ensuring that our production processes and cleanroom environments comply with validation and qualification standards. We take pride in our commitment to precision, efficiency, and continuous improvement adhering to...

Company Overview:Ferrosan Medical Devices A/S is a rapidly growing company with a unique impact on global healthcare. Our production processes are designed to ensure precision, efficiency, and continuous improvement adhering to Lean methodologies. We take pride in our commitment to improving patient outcomes and taking care of each other, our environment,...

About the RoleWe are seeking a highly skilled Data Governance Specialist to join our R&D Data Governance Office at Novo Nordisk. As a Quality & Compliance Partner, you will play a key role in overseeing quality and compliance initiatives related to Data Governance.Your primary responsibilities will include driving initiatives that support the identification,...

We are looking for a talented Health Regulatory Compliance Specialist to support our innovation and compliance efforts within our Health division. As a member of our Regulatory team, you will be responsible for ensuring ongoing regulatory and product safety compliance of our existing product portfolio.Key ResponsibilitiesCollaborate with Global teams and...

Drive Success as a Lead Quotation SpecialistIn this critical role, you will lead the way in developing and managing quotations for our global GPHE project business. As a key stakeholder, you will work closely with cross-functional teams to drive success and achieve business objectives.Key Accountabilities:Develop and manage quotations that meet customer...

About the RoleWe are seeking an experienced Biologics Quality Assurance Specialist to join our QMS & Training team in the Quality Systems department. As a key member of our team, you will collaborate with partners and drive improvement projects optimizing our GMP Training standards and systems.Your primary responsibility will be to develop new training...

About Again BioWe are addressing a global environmental challenge by developing novel carbon-negative chemical solutions. Our technology converts industrial emissions into valuable, emission-free green chemicals.Our innovative approach enables the removal of over 2 tonnes of carbon from the atmosphere for every tonne of product we make.Job OpportunityAgain...

E.ON Drive Infrastructure (EDRI) is a leading European provider of public charging infrastructure for electric vehicles, committed to creating a sustainable world by offering charging solutions everywhere.Job OverviewThis role involves supporting the smooth operation of our office, encompassing a variety of tasks:Executing errands: Picking up and delivering...

At AGC Biologics, we strive to bring hope to life by enabling therapies for patients worldwide.About the RoleThis is a leadership position that involves guiding a team of dedicated QC HPLC Scientists in method validations, analytical data generation, and customer interactions.The successful candidate will lead a unit of 10 skilled scientists working closely...

About the RoleAs a CMC Regulatory Specialist at Novo Nordisk, you will provide strategic, tactical, and operational regulatory input to projects. You will lead activities for synthetic small molecule projects in late development as well as drive scientific and regulatory discussions across our portfolio.In this role, you will work closely with stakeholders...

Role Summary:We are seeking a highly skilled Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist to join our team at Novo Nordisk A/S.In this role, you will be responsible for providing strategic regulatory input to projects, including developing regulatory strategies for submission of clinical trial applications (CTAs) and marketing...

AGC Biologics is a global Contract Development and Manufacturing Organization (CDMO) dedicated to bringing hope to life by enabling life-changing therapies for patients around the globe. We create a healthier and happier tomorrow through our work side by side with customers to improve patients' lives by bringing new biopharmaceuticals to market.We develop...

Job OverviewWe are seeking a highly motivated and organized individual to join our Digital Health & Staffs Quality department at Novo Nordisk. As a key member of our team, you will be responsible for creating and maintaining a quality-focused and compliant Customer Service framework that supports the company's continuous growth and focus on patients...

Job Overview:We are Reckitt Benckiser, a global leader in health, hygiene, and home products. We are seeking an experienced Regulatory Affairs Associate to join our team.The ideal candidate will have a strong understanding of regulatory environments and processes in the Nordics, with a minimum of 2 years of experience in EU chemical, detergent, biocide, and...

At Novo Nordisk A/S, we are seeking a skilled Safety Surveillance Specialist to join our team.About the PositionYou will be responsible for establishing and maintaining product safety profiles during development and post-approval phases. This includes conducting safety surveillance of Novo Nordisk products based on worldwide safety information...

About European Energy:We are a Danish privately owned company founded in 2004 with headquarter in Copenhagen. We operate all the way from development, design, financing, construction, operation and selling of wind- and solar farms on land as well as offshore globally. Our core values are the foundation of everything we do: In it together, Trust and courage,...

Novo Nordisk A/S is a dynamic company that drives change in the pharmaceutical industry.About the RoleWe are seeking a skilled Safety Surveillance Specialist to join our team and contribute to the development of safe and effective pharmaceutical products.Key ResponsibilitiesYour key responsibilities will include:Establishing and maintaining the product...