Regulatory Affairs Expert, Health and Compliance

At Reckitt Benckiser, we protect, heal, and nurture in the relentless pursuit of a cleaner, healthier world. Our purpose defines why we exist: to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.About the RoleThis Regulatory Affairs Associate position is part of our dynamic Hygiene team. As a key member,...

About the RoleWe are seeking a skilled Regulatory Affairs Specialist to join our team at Novo Nordisk A/S. As a key member of our RA CMC Synthetics & Cell Technologies department, you will play a crucial role in driving regulatory affairs strategies and submission activities related to synthetic small molecule projects.ResponsibilitiesProvide strategic,...

Unlock your potential as a Regulatory Affairs Specialist in a dynamic role at Novo Nordisk A/S, where you will drive the planning and optimization of global regulatory strategies.About the RoleWe are seeking a highly skilled and experienced professional to join our Regulatory Affairs CMC & Device team in Søborg, Denmark. As a Strategic RA Planning...

Secure a Career in Supply Chain Management with Ferrosan Medical DevicesFerrosan Medical Devices A/S is a rapidly growing company focused on improving patient outcomes through innovative healthcare solutions. As a Compliance Partner, you will play a crucial role in ensuring the compliance of our suppliers, contract manufacturers, and service providers.About...

About the RoleWe are seeking a highly skilled Regulatory Compliance Specialist to join our team at AGC Biologics in Copenhagen Site. This is an exciting opportunity to work in a dynamic and fast-paced environment, contributing to the success of our manufacturing operations.Job SummaryThe QA Manufacturing Support Scientist will be responsible for ensuring...

About AGC Biologics">AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and...

We are looking for a highly motivated and experienced process optimization lead to join our regulatory affairs team at Novo Nordisk A/S. As a key member of our team, you will be responsible for driving process excellence, innovation, and digital transformation in a regulated global environment.The ideal candidate will have a strong background in life...

We are seeking a highly skilled Patient-Centric Drug Development Specialist to join our team at Novo Nordisk A/S. This is an excellent opportunity to contribute to the development of innovative treatments for patients with serious chronic diseases.About the RoleIn this role, you will play a pivotal part in developing and implementing clinical outcome...

About the RoleWe are seeking an experienced Clinical Writing Expert to join our team in Clinical Reporting at Novo Nordisk A/S. As a key member of our team, you will be responsible for driving the preparation of complex clinical documents and serving as a project manager.Main Responsibilities:Lead tasks such as planning, development, and oversight of...

About AGC BiologicsAGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral...

OverviewAGC Biologics, a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO), is seeking a talented Process Transfer Scientist to join its dynamic team in Copenhagen. As a key member of the MSAT unit, this role offers an exciting opportunity to work with cross-functional teams and contribute to the successful transfer...

About the OpportunityWe are seeking a highly skilled Senior Digital Health Solutions Project Lead to join our team in Søborg, Denmark. This is an exciting opportunity to drive agile product development from idea to go-live, working closely with internal stakeholders and external partners.Key ResponsibilitiesLead project teams of 5-8 members, translating...

Obesity Clinical Development LeadThis is an exciting opportunity for a seasoned medical professional to join our team as a Clinical Development Lead in the Obesity area. As a key member of our Medical & Science department, you will be responsible for driving the planning and execution of global clinical studies and providing medical oversight during study...

We are seeking a seasoned Corporate Legal Leader to spearhead our Product Supply Quality & IT (PSQIT) unit's legal strategy and operations.About the RoleAs the Legal Director for our PSQIT Manufacturing & Ethics team, you will be responsible for providing strategic legal guidance to various units, including API Kalundborg, Finished Production Manufacturing,...

About the PositionAt Novo Nordisk, we are seeking a highly skilled Quality Assurance Specialist to join our team. As a key member of our Digital Health & Staffs Quality department, you will be responsible for ensuring the quality and compliance of our customer service processes.Your Key ResponsibilitiesProcess Design and Implementation: Provide QA input on...

About the RoleWe are seeking a skilled Strategic Procurement Expert to join our dynamic team at Novo Nordisk A/S. This is an exciting opportunity to drive successful outcomes and make a difference in the world of healthcare.Job SummaryThe Advanced Procurement Professional will be responsible for governing the procurement process, purchasing goods and...

We are seeking a seasoned clinical professional to spearhead the development of innovative treatments for rare blood disorders.About the RoleThis is an exciting opportunity for a medical expert with a strong background in haematology and experience in clinical drug development to take on a leadership position at Novo Nordisk.The successful candidate will be...

About the RoleWe are seeking a highly motivated and experienced Quality Assurance Professional to join our CMC API QA team at Novo Nordisk A/S. As a key member of our team, you will be responsible for ensuring compliance with regulatory requirements, quality standards, and company policies in the raw material and CMO shipping area.ResponsibilitiesDeliver...

We are seeking a highly motivated and experienced Quality Assurance Professional to join our CMC API QA team at Novo Nordisk A/S, based in Bagsværd, Denmark.The successful candidate will serve as QP delegate, primarily responsible for releasing internal and externally produced Active Pharmaceutical Ingredients (API) for usage in the Novo Nordisk clinical...

About AGC BiologicsAGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way.We provide world-class development and manufacture of mammalian and...