Senior Quality Improvement Specialist

About Novo Nordisk\Novo Nordisk A/S is a dynamic business area that produces Active Pharmaceutical Ingredients (API) for patients across the world. Our site in Hillerød is an innovative and fast-growing production site with over 4,000 talented employees.\The Role\We are looking for a senior compliance coordinator who knows this role well and can drive...

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...

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,...

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...

About the JobWe are seeking a highly skilled Quality Specialist to join our team of professionals dedicated to ensuring the highest quality standards of our products. As a key member of our team, you will play a pivotal role in driving improvement and standardisation across the organisation.Key ResponsibilitiesDefine, monitor, and improve activities,...

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...

About the RoleThe Director of Operational Excellence will be responsible for overseeing the daily operations of our laboratory, ensuring that all tasks are completed efficiently and effectively. This includes managing a team of chemists and laboratory technicians, as well as developing and implementing processes to improve operational efficiency.Key...

About UsNovo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Our commitment to innovation and quality has made us one of the 20 most valuable companies in the world by market cap.Our ValuesWe recognise the importance of the unique skills and perspectives our people bring to the...

Job OverviewAseptic quality assurance is a critical component of pharmaceutical production. As an Aseptic Quality Assurance Specialist at Novo Nordisk, you will play a vital role in ensuring the quality and safety of our products. This position requires a strong understanding of pharmaceutical manufacturing processes and regulations.Key Responsibilities-...

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...

Job DescriptionThe role of Senior GMP Expert in Novo Nordisk A/S's DMD, Product Control & Global Support department involves managing various quality-related activities across the department, occasionally also across DMD.As a member of this team, you will be responsible for ensuring a high level of quality and compliance within Product Control and Global...

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 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...

At Fujifilm Diosynth Biotechnologies, we are committed to developing and manufacturing innovative biological products. As a leading Contract Development and Manufacturing Organization (CDMO), our goal is to provide high-quality services that meet the needs of our clients.About the RoleWe are seeking a dedicated Quality Assurance specialist to join our audit...

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...

Company OverviewWe are a dynamic biopharmaceutical company with a vision to defeat chronic diseases. We drive change and innovation in the industry, prioritizing quality and safety.

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 Title: Senior Global Quality StrategistWe are seeking a seasoned professional to enhance the effectiveness of our KojoX QC strategy at FUJIFILM Diosynth Biotechnologies.Key Responsibilities:Liaison Role: Serve as a key liaison between the global QC VP and internal/external stakeholders, translating the QC KojoX vision and goals into actionable...

About the RoleThe GMP Coordinator will be responsible for maintaining a high level of compliance with cGMP and Novo Nordisk's Quality Management System. This involves supporting the department in developing and maintaining a robust quality management system, ensuring that all processes and procedures are in place to meet regulatory requirements.Key...

Job Description\We are seeking a highly skilled Senior Validation Engineer to join our team at the Site Hillerød production site. As a Senior Validation Engineer, you will play a critical role in ensuring the quality and safety of our products by validating complex manufacturing equipment and processes.\This position has three main areas of...