Regulatory Compliance Expert

Are you passionate about shaping the future of your area? Do you want to contribute to the development and scaling of our Complaints, Inspections & Audit processes?We are seeking a highly skilled and experienced Senior QA Professional to join our team at Novo Nordisk A/S. The ideal candidate will have a strong background in quality assurance, regulatory...

Ferrosan Medical Devices A/S is a leading manufacturer of medical devices used in surgical care. Our products are designed to minimize bleeding challenges in surgery and electromechanical medical devices for performing breast biopsies. We're committed to improving patient outcomes and take our values to work every day – we care about each other, our...

About the RoleWe are seeking a highly skilled and experienced QA Specialist to join our team in Clinical Trials. As a member of our Quality Assurance department, you will play a crucial role in ensuring the quality and safety of products for clinical trials. In this dynamic environment, you will work closely with our team of experts to deliver best-in-class...

At AGC Biologics, we strive to maintain a positive and proactive work environment that fosters close collaboration between teams. Our company culture emphasizes professionalism, flexibility, and a focus on delivering exceptional results.We are seeking an experienced QA professional to join our Material Management team. In this role, you will be responsible...

Job SummaryWe are looking for a highly motivated and detail-oriented Compliance Engineer to join our team. As a Compliance Engineer, you will play a key role in ensuring that our facilities and processes meet regulatory requirements.About the PositionYou will be part of the Plant Engineering department, responsible for implementing and maintaining quality...

Come work at the forefront of science - and help the brands you grew up with grow and evolve into the next generation. Job Description - Senior Regulatory Affairs Specialist (2507030367W) Who we are At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands —...

About the TeamThe RA Process and Digital Strategy area within Regulatory Affairs is a growing team of 10 people, committed to securing process excellence and digital innovation to reach more patients faster.We work across the value chain from early development to product discontinuation, ensuring medicine availability to patients. Our team is based at our...

About the DepartmentDigital Transformation is a department placed in RQ&C: RQ&C consists of the four functional areas: Regulatory Affairs (approvals by health authorities), R&D Quality (ensuring quality and compliance), Clinical Reporting (medical writing) and Digital Transformation (driving the Digital agenda). Furthermore, our department also supports the...

About the RoleWe are seeking a highly motivated and organized QC Coordinator/Analytical Project manager to join our QC Chemistry team. The successful candidate will be responsible for supporting the production of new or marketed biopharmaceuticals by performing analytical testing and validating various analytical procedures according to ICH guidelines from...

Kenvue is committed to delivering high-quality products that meet the needs of consumers worldwide. As a Global Product Approvals Manager, you will be responsible for securing approvals for new products, line extensions, and additional claims, while supporting business objectives.The ideal candidate will have expertise across a broad spectrum of Regulatory...

Job DescriptionThis role offers a unique opportunity to join a dynamic team in a fast-paced, global environment. As a CMC Regulatory Specialist, you will play a critical role in ensuring the successful development and approval of our synthetic small molecule projects. Your expertise in regulatory affairs, combined with your knowledge of synthetic small...

About the JobWe are seeking a highly skilled Compliance Engineer to join our team in Copenhagen. As a Compliance Engineer, you will be responsible for ensuring that our facilities and processes meet regulatory requirements.About the DepartmentThe Plant Engineering department is responsible for executing technical projects and overseeing the operation of all...

Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Join our dynamic team and make a significant impact in the realm of RA Business Compliance. We're seeking a talented individual who can effortlessly unravel complex data challenges, deliver impeccable data transparency, and contribute to enhancing overall...

About the TeamThe RA Process and Digital Strategy area within Regulatory Affairs is a growing team of 10 people. We are committed to securing process excellence and digital innovation to reach more patients faster by standardising ways of working with a focus on end users.Our mission is to make work easier and more rewarding for our colleagues. In Regulatory...

Select how often (in days) to receive an alert: Create AlertCategory: Reg Affairs & Safety PharmacovigilanceLocation: Søborg, Capital Region of Denmark, DKWe are expanding our product and project pipeline in Novo Nordisk and are looking for an engaged Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic...

Job DescriptionWe are seeking an experienced Clinical Trial Operations Manager to join our team at Novo Nordisk A/S. As a Clinical Trial Operations Manager, you will be responsible for overseeing the submission of clinical trials to regulatory authorities worldwide.The successful candidate will have extensive experience in project management, with a strong...

Job SummaryWe're looking for a highly skilled Regulatory Compliance Expert to join our team. As a Regulatory Compliance Expert, you'll be responsible for ensuring that all aspects of our business operations comply with relevant laws and regulations.Your Key ResponsibilitiesYou'll advise on Quality Management System and external regulations.You'll handle and...

Would you like to drive initiatives that innovate compliance procedures through digitalization and process improvement within the pharmaceutical industry? Do you want to be at the forefront of ensuring quality and compliance in handling clinical & research data and enhancing operational efficiency in a truly global organization? If so, then you might be the...

Would you like to drive initiatives that innovate compliance procedures through digitalization and process improvement within the pharmaceutical industry? Do you want to be at the forefront of ensuring quality and compliance in handling clinical & research data and enhancing operational efficiency in a truly global organization?If so, then you might be the...

Are you passionate about working with data? Do you want to set directions and deliver results? Do you have the ability to handle complex tasks? If yes, we are seeking an experienced and highly motivated Regulatory Data Partner to join our team, who will be responsible for implementing and supporting our data in the Regulatory organisation, and support...