API Quality Improvement Specialist

We are seeking a seasoned Senior GMP Coordinator to join our dynamic team in API Manufacturing 4, 25K Multi Product Facilities. As a key member of our quality-focused group, you will play a pivotal role in driving quality-related improvements, audits, and inspections within our department.Your primary responsibilities will include:Planning, preparing,...

Fujifilm Diosynth Biotechnologies Denmark is expanding its Quality Control department, and this presents a fantastic opportunity to join our vibrant team as a Quality Assurance Specialist for Compliance and Process Improvement.Located in Hillerød, our Quality Control department comprises approximately 230 employees across five testing teams and five support...

At Novo Nordisk A/S, we are seeking a highly skilled Senior GMP Expert to join our Device Manufacturing Development (DMD), Product Control and Global Support department.The successful candidate will have a strong understanding of Good Manufacturing Practices (GMP) regulations and requirements, with practical experience in the pharmaceutical industry. They...

Company OverviewNovo Nordisk A/S is a leading biotech company specializing in the production of Active Pharmaceutical Ingredients (APIs). Our mission is to improve patient care by delivering innovative solutions.

About the RoleWe are looking for an experienced Quality Assurance Specialist to join our team in Hillerød. The successful candidate will be responsible for ensuring the quality strategy is implemented and adhered to, both internally and externally.Key ResponsibilitiesDevelop and implement quality strategies to ensure compliance with regulatory...

Novo Nordisk A/S is a life-science company dedicated to ensuring that people can lead a life independent of chronic disease. Our Assembly in Hillerød department focuses on increasing production capacity while maintaining high quality standards and employee well-being.We are seeking a Quality Assurance Specialist to support both management and colleagues on...

About the RoleAs a Lead Process Improvement Specialist in our Primary Packaging Development department, you will play a pivotal role in driving process excellence and strategic direction for container closure development. Your primary focus will be on understanding user needs, addressing process gaps, and collaborating with cross-functional teams to ensure...

Job DescriptionWe are seeking a skilled Pharmaceutical Process Engineer - Regulatory Compliance Specialist to join our team at Novo Nordisk A/S. As a key player in the Validation Support team within the Project Quality Management (PQM) department, you will be responsible for ensuring that validation structures and processes are robust and effective.In this...

About the DepartmentThe DCM Device Metrology & QC team is responsible for ensuring the quality and reliability of our plastic components. We use advanced measurement technologies to ensure that our products meet the highest standards of quality.As a Metrology Engineer on our team, you will be part of a dynamic and collaborative group of professionals who are...

About the JobWe are seeking an experienced Quality Control Specialist to join our DCM Device Metrology & QC team. As a key member of this team, you will be responsible for ensuring the quality and reliability of our plastic components.The ideal candidate will have a strong background in quality control, with experience working in a GxP controlled...

Job Overview\At Novo Nordisk A/S, we are committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve, and the communities we operate in. As a senior compliance coordinator, you will play a key role in driving quality-related improvements and ensuring compliance with regulatory...

About the RoleAs a Senior QC Equipment Chemist, you will play a key role in ensuring the quality of raw materials and excipients used in the production of Novo Nordisk's products. You will be part of the Sourcing QC department, which is responsible for ensuring the quality of raw materials, excipients, and packaging materials.The position is within one of...

FUJIFILM Diosynth Biotechnologies is a world-leading Contract Development Manufacturing Organization (CDMO) providing services to the pharmaceutical industry. Our mission is to 'Advance Tomorrow's Medicines.'The company offers a dynamic and collaborative work environment with opportunities for professional growth and development.We are seeking a skilled...

About Fujifilm Diosynth BiotechnologiesWe are an advanced biotech company that develops and manufactures leading biological products on the market today and for the future.As a leading CDMO within our areas of expertise, we aspire to be at the forefront of innovation and quality in the industry.

Job SummaryWe are seeking a highly motivated Quality Assurance Manager to join our team in Hillerød. The successful candidate will be responsible for leading the quality assurance function and ensuring that all quality-related activities are executed effectively.Main ResponsibilitiesDevelop and implement quality strategies to ensure compliance with...

Job OverviewAs a Transformation Specialist for Process Enhancement at FUJIFILM Diosynth Biotechnologies, you will play a pivotal role in driving continuous improvement across our organization.Key ResponsibilitiesProject Leadership: You will lead the design and implementation of tech transfer improvement projects from conception to completion, ensuring...

Job DescriptionWe are seeking a highly skilled Advanced Quality Assurance Professional to join our team in Hillerød. The successful candidate will be responsible for ensuring the quality strategy is implemented and adhered to, both internally and externally.The PositionHandle cases related to production on automated inspection lines and Environmental...

Job OverviewWe're seeking a highly skilled Advanced Process Engineer to join our Global Finished Product Supply (GFPS) team. As a key member of this team, you'll play a critical role in supporting our global production operations and ensuring the highest quality standards are met.In this position, you'll have the opportunity to work on various projects,...

Job Overview:Compliance Specialist - Device DevelopmentWe are looking for a highly skilled Compliance Specialist to work in our Device Development team at Novo Nordisk A/S. The successful candidate will be responsible for analysing and guiding the implementation of health authorities' regulations on our marketed product portfolio. This is a challenging and...

Job DescriptionWe are seeking a highly skilled Quality Assurance Technician to join our team in Global Contract Manufacturing (GCM) Devices, External Batch Release.