Regulatory Reporting Specialist

Career Opportunities at Saxo Bank A/SCompany Overview:Saxo Bank A/S, a leading international online trading and investment specialist, is seeking a highly motivated Tax Compliance Specialist to join our Group Compliance team.Job Description:The successful candidate will play a key role in supporting the business in meeting regulatory requirements within the...

Copenhagen, Denmark About the Job: Would you like to be part of an ambitious compliance team where you will play an important role in supporting the business meeting regulatory requirements in a dynamic and international environment? If so, we have the right opportunity for you in Saxo Bank. We are growing our team in Group Compliance and are looking for a...

Copenhagen, Denmark About the job Are you motivated by working in a dynamic environment with a steep learning curve alongside colleagues on complex regulatory requirements? Then join us as our new Tax Reporting Associate where you will be part of the Global Tax Reporting team and help us manage the global tax landscape on behalf of Saxo’s clients and...

Copenhagen, Denmark About The Job Group Internal Audit (GIA) in Saxo is responsible for carrying out risk-based operational audits across the organisation and its subsidiaries. Reporting directly to the Board of Directors, GIA helps to ensure that the organisation effectively manages and mitigates the risks associated with its business activities. We are...

Job Details: Regulatory Affairs Senior Specialist Job Title: Regulatory Affairs Senior Specialist Vacancy No: VN1967 Category: Clinical, Medical and Regulatory Affairs Contract Type: Permanent Contract Duration: Full Time Location: Vejle Job Advert: Fertin Pharma has ambitious plans to grow our business in established markets (North America and...

Select how often (in days) to receive an alert: Create Alert Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Are you driven by the challenge of ensuring effective planning for regulatory submissions worldwide? Do you seek an exciting opportunity to shape global regulatory LCM strategies and contribute to...

Select how often (in days) to receive an alert: Create Alert Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK We 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...

Regulatory Affairs Specialist, IVDR Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do...

Join us in this role where you’ll spearhead the development and implementation of global direct and indirect tax compliance strategies, ensuring adherence to all relevant regulations. You will lead a dedicated team, providing strategic advice and enabling continuous development of relevant highly skilled tax specialists to deliver tax efficient in-house...

Senior Specialist, CMC Drug Product Formulation Development Are you passionate about drug product formulation development? Do you have extensive experience in pharmaceutical development from Biotech or Pharmaceutical industry? If so, now is your chance to join Ascendis Pharma as our new senior specialist for CMC Drug Product Formulation Development. Ascendis...

Copenhagen, Denmark About the job Do you want to be part of a newly established AML Requirements team in a Financial Crime Prevention? This is an exciting opportunity to join the Financial Crime Prevention organisation where the culture is informal, professional and engaged. Collaboration, flexibility and a results-driven approach are key for success....

Ascendis Pharma A/S , a visionary and ambitious company, offers you an opportunity to become a participant in the further establishment and effective operation of the QA Commercial department. You are offered a position with potential to grow your professional and personal skills and to be part of the handling of new products and new markets. You will be...

Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a...

Are you an experienced Medical Writer looking to grow your career? If yes, then we would love to hear from you. The position As Medical Writing Specialist, your main responsibility is to drive the preparation of complex clinical documents and act as project manager. More specifically, you are expected to lead tasks such as: Planning, development and...

Company Overview"Tietoevry creates purposeful technology that reinvents the world for good. We are a leading technology company with a strong Nordic heritage and global capabilities. Our core values of openness, trust, and diversity drive our work with customers to develop digital futures where businesses, societies, and humanity thrive."Job Description"We...

We are seeking an experienced Aseptic Technology Standards Specialist to join our team at Novo Nordisk A/S. In this role, you will be responsible for developing technology standards for aseptic production lines worldwide, ensuring global consistency and best practices.About the RoleAs a member of the Fill & Finish Expansions department, you will work closely...

Field Action Specialist Job Description The Global Quality and Regulatory Affairs (GQRA) Field Action Specialist’s responsibilities include managing Field Action Activities such as leading Field Action Strategy and Field Safety Communication meetings, recalls, field notifications, and correction processes for medical and non-medical products. Duties...

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...

OverviewAscendis Pharma A/S is a fast-growing biopharmaceutical company with operations in Denmark, Germany, and the United States. We are dedicated to developing innovative therapies to address unmet medical needs.Job DescriptionAs a Senior GCP Quality Assurance Specialist, you will play a critical role in ensuring compliance with Good Clinical Practice...

Select how often (in days) to receive an alert: Create Alert Clinical Outcome Assessment Specialist - Parental Leave Cover Category: Clinical Development Location: Søborg, Capital Region of Denmark, DK Would you like to be a part of the ambitious journey towards ensuring that patients’ experiences, perspectives, needs, and priorities are captured and...