Medical Specialist

Job DescriptionFerrosan Medical Devices A/S is a leading provider of medical devices used in surgical care. We are seeking an experienced Medical Device Quality Assurance Specialist to join our team.About the RoleThe successful candidate will be responsible for ensuring the highest quality of our medical devices, working closely with various teams to ensure...

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...

Do you want to be a part of our Quality Control team in a successful company with a unique impact on global healthcare? Grab this opportunity to join a rapidly growing company, ready to invest in you. Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own...

Company OverviewFerrosan Medical Devices A/S develops and produces a portfolio of medical devices used in surgical care. Our products help minimize bleeding challenges in surgery and perform breast biopsies.Job DescriptionWe are seeking a Quality Control Specialist to join our team. As a Quality Control Specialist, you will be responsible for daily support...

Jobbeskrivelse Placering Søborg, Denmark Jobkategori Clinical Development Are you passionate about innovative Clinical Drug Development with a keen eye for Haemoglobinopathies? Would you drive change for patients with Rare Diseases and relish the chance to be medically responsible for the clinical development strategy for a clinical-stage asset for...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

Direct message the job poster from CM Medical Recruitment Connecting Top-tier Talent with Opportunities in the Medical Device Industry CM Medical have partnered with an innovative company specializing in developing advanced software that leverages artificial intelligence to analyze microscope images, primarily for medical research and diagnostics. Their...

Are you passionate about innovative Clinical Drug Development with a keen eye for Haemoglobinopathies? Would you drive change for patients with Rare Diseases and relish the chance to be medically responsible for the clinical development strategy for a clinical-stage asset for patients with Sickle Cell Disease or Thalassemia? With limitless opportunities for...

Would you like to be a part of the ambitious journey towards ensuring that patients’ experiences, perspectives, needs, and priorities are captured and meaningfully incorporated into drug development and evaluation? Are you ready to shape the future of clinical trials through clinical outcomes assessment (COA)? Do you thrive in cross-functional...

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...

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market. About the Job Do you thrive in a fast-paced environment? Are you...

We are looking for a talented Health Regulatory Compliance Specialist to support our innovation and compliance efforts within our Health division. As a member of our Regulatory team, you will be responsible for ensuring ongoing regulatory and product safety compliance of our existing product portfolio.Key ResponsibilitiesCollaborate with Global teams and...

About AGC BiologicsWe are 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.Our mission is to work together with our customers to improve patients' lives by bringing...

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...

Company OverviewNovo Nordisk A/S is a dynamic pharmaceutical company that operates in the global medical affairs sector. Our team develops and implements supporting initiatives to ensure successful patient recruitment and retention in clinical trials.About UsWe're committed to excellence without fixating on perfection, embracing experimentation and...

About ReckittWe are a global team united by our purpose to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are home to the world's best loved and trusted hygiene, health, and nutrition brands.The RoleAs a Compliance Specialist in our Regulatory Affairs department, you will be responsible for ensuring on-going regulatory...

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...

Job DescriptionThe role of Quality Specialist with expertise within In-Vitro Diagnostics is a key position in the RDQ Operational Excellence department at Novo Nordisk A/S.Key ResponsibilitiesEnsure compliance with IVD regulations and other relevant requirements.Act as a Quality Partner and support key projects with IVD solutions.Collaborate with...

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...

Job Description 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 best: improve the world...