GMP-kvalificeringsmedarbejder

About the RoleWe are seeking a highly skilled GMP Compliance Specialist to join our team at Novo Nordisk A/S. As a Senior Quality Assurance Leader, you will play a critical role in ensuring adherence to Good Manufacturing Practice (GMP) compliance requirements and best practices across all operations in Local Manufacturing.In this position, you will provide...

We are seeking a talented Senior Scientist to join our Quality Assurance team as a GMP Compliance Expert. In this role, you will be responsible for ensuring the quality and compliance of our biopharmaceutical production processes.Your Key Responsibilities:Develop and implement quality management systems to ensure continuous improvement.Collaborate with...

Select how often (in days) to receive an alert: Create Alert Would you like to take the next exciting step in your career by playing a key role in a dynamic and impactful business support unit, driving meaningful change in Local Manufacturing production? Does using your hands-on expertise in deviation handling and cGMP to tackle tasks, enhance processes, and...

Job SummaryThe GMP Compliance Specialist plays a critical role in ensuring that the Chemistry Pilot Plant at Novo Nordisk PSQIT organization meets all regulatory requirements. This includes driving quality-related tasks and projects across the department, coordinating and implementing cross-functional quality projects, and setting quality goals for the...

At Genmab, we're committed to building extraordinary futures together, by developing antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being...

About LundbeckLundbeck A/S, H is a leading global pharmaceutical company that specializes in the development and production of innovative treatments for brain disorders. Our team is passionate about making a difference in the lives of those affected by neurological and psychiatric disorders.The role you are applying for is a critical part of our efforts to...

As a Process Specialist at European Tech Recruit, you'll be responsible for designing, specifying, and overseeing the installation of new process equipment. You'll provide technical support and troubleshooting for Upstream (Cell Culture), Downstream (Purification), Clean Utility/CIP, and Solution Preparation systems.About the Job FunctionThe ideal candidate...

About UsWe are part of the Novo Nordisk PSQIT organization, Chemistry, Manufacturing and Control (CMC) Product & Process Development, making a real difference for patients with chronic diseases across the world.We develop, manufacture, and distribute drug candidates for clinical trials and have a strong culture with a 'can-do' mindset. The cell banks in Novo...

About the Position"> We are seeking a highly motivated and experienced Regulatory Affairs professional to join our team as a Pharmaceutical QA Lead. The successful candidate will be responsible for ensuring compliance with EU and US regulations, reviewing and authoring QMS SOPs, Work Instructions, and other documents, and supporting Quality Management...

About the Role:We are seeking an experienced Analytical Specialist to join our GMP laboratory. The successful candidate will be responsible for ensuring the quality of analytical procedures for new injectable drug products.The role involves supporting chemical analysis of injectable drug products, both internally in the department and globally in QC...

Passionate about Quality Assurance with expertise within outsourced GMP activities and development projects?Ascendis Pharma invites you to explore the role of our newest QA Specialist / QA Professional for Development GMP activities.With roots spanning Denmark, Germany, and the United States, Ascendis Pharma A/S emerges as an innovative and dynamic...

About the PositionWe are seeking a highly skilled Deviation Management Expert to join our team at Novo Nordisk A/S. As a Senior Quality Assurance Leader, you will play a critical role in ensuring adherence to Good Manufacturing Practice (GMP) compliance requirements and best practices across all operations in Local Manufacturing.In this position, you will...

Job DescriptionWe are looking for a highly skilled Senior Quality Assurance Leader to join our team at Novo Nordisk A/S. As a Deviation Management Expert, you will play a critical role in ensuring adherence to Good Manufacturing Practice (GMP) compliance requirements and best practices across all operations in Local Manufacturing.In this position, you will...

Ansættelse i Quality AssuranceALK søger en dedikeret kvalificeringskonsulent til Quality Assurance Production Support teamet. Du vil være ansvarlig for at sikre, at ALK lever op til gældende standarder indenfor GMP.**Om stillingen**I rollen som kvalificeringskonsulent vil du supportere vores stakeholders med at sikre ALKs GMP-forpligtigelser ift....

About the Role"> We are seeking a highly skilled and experienced Quality Assurance (QA) professional to join our team as a GMP Compliance Specialist. The successful candidate will be responsible for ensuring the quality of our commercial products, including biological and chemical GMP production. Key responsibilities will include maintaining and improving...

As a Clinical Drug Supply Manager at Genmab, you will play a critical role in ensuring the success of our clinical trials. You will be responsible for managing the outsourcing of packaging, labeling, and distribution of clinical trial supplies for early- and late-stage trials. The successful candidate will work closely with GMP QA and our CMOs to ensure...

European Tech Recruit is seeking a highly skilled Process Specialist to join our dynamic project team working with cutting-edge biopharmaceutical manufacturing technologies in the Greater Copenhagen area.About the RoleThis is an exciting opportunity for an experienced professional with a background in GMP manufacturing, engineering, and process optimization....

Karrierechance som teknikerkonsulentHvis du er interesseret i karriere som teknikerkonsulent, så søger vi dig!Vi søger dygtige teknikere, som har erfaring fra det praktiske arbejde i et anlæg og kan udarbejde GMP-forskrifter og dokumentation.Vi tilbyder en spændende og afvekslende hverdag i et åbent og dynamisk arbejdsmiljø med rige muligheder for...

About the RoleThe successful candidate will possess excellent skills and knowledge in quality assurance documentation, particularly in the pharmaceutical industry. You will be responsible for ensuring that all documentation meets the required standards and regulations.Main responsibilities:Maintaining accurate and up-to-date documentationConducting technical...

Job DescriptionThe Pharmaceutical Development Engineer will play a crucial role in supporting our manufacturing, process optimization, and regulatory compliance projects in Denmark. As an expert in process engineering, you will be responsible for developing and optimizing production processes for medical devices, pharmaceuticals, and biotech products.You...