Regulatory Compliance Specialist

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...

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 —...

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...

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...

About the RoleWe are seeking an experienced Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic small molecules to join our team. As a key member of our regulatory affairs department, you will provide strategic, tactical, and operational regulatory input to projects. Your responsibilities will include...

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...

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...

The Ideal CandidateWe are looking for an experienced Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic small molecules to join our team. The ideal candidate will have a Master's and/or Ph.D. degree in life sciences with regulatory CMC experience either from the pharmaceutical industry or from a health...

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...

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...

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 PositionWe're seeking a Quality Assurance Specialist to join our Digital Health & Staff Quality team. As a key member of this team, you'll be responsible for quality oversight and support for Complaints, Audits & Inspections.Your Key ResponsibilitiesYou'll handle and approve deviations and document updates.You'll participate in process...

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 This RoleWe are seeking an experienced Clinical Trial Submission Manager to join our CTA Management department. As a key member of our team, you will be responsible for leading the submission of initial Clinical Trial Applications (CTAs) and amendments to Health Authorities (HAs) and Ethics Committees (ECs). You will collaborate closely with...

We are passionate about connecting the Medical & Science organization while driving scientifically sound medical deliverables across the Novo Nordisk project portfolio. As a Clinical Outcome Assessment Specialist, you will be part of this ambitious journey towards ensuring that patients' experiences, perspectives, needs, and priorities are captured and...

Safeguarding Our ReputationAs a QHSE professional, you will play a critical role in safeguarding our reputation by ensuring the highest standards of quality, health, safety, and environmental management across our operations. You will lead a skilled team of QHSE specialists, driving innovation and excellence in our pursuit of becoming the most innovative...

About Novo Nordisk:Novo Nordisk A/S is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Our success relies on the joint potential and collaboration of our more than 69,000 employees around the world. We recognize the importance of unique skills and perspectives our people bring to the table.Key...

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...

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...

Select how often (in days) to receive an alert: Create Alert (Senior) Regulatory Affairs Professional, RA Obesity - Maternity cover Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Do you have a talent for navigating complex regulatory landscapes and driving strategic initiatives? Are you eager to contribute...