Pharma Documentation Specialist

Job OverviewLeverage your expertise as a Senior Case Management Specialist to drive the success of our Global Safety Surveillance team at LEO Pharma. As a key member of our team, you will be responsible for managing and leading a team of Global Safety Advisors and Safety Leads, ensuring compliance with pharmacovigilance processes, regulations, and...

Join us at Novo Nordisk A/S as an IT Responsible in Digital, Data & IT (DD&IT) in Bagsværd. This role presents a fantastic opportunity to contribute to the growth and development of our new department, which supports projects and existing equipment in the Aseptic Manufacturing Facility.As an IT Responsible, you will play a vital role in ensuring the highest...

The Ubique Systems' IT Compliance Lead will define and execute a validation strategy for the development and implementation of a Non-GxP SaaS solution, Genetics Analysis Platform. The role is responsible for ensuring that systems are in compliance with internal and external regulatory requirements.Key responsibilities include delivering end-to-end...

Quality Assurance Documentation Engineer 3 days ago Be among the first 25 applicants Direct message the job poster from Think IT Resources Recruitment Consultant at Think IT Resources I am currently looking for a Quality Assurance Documentation Consultant, someone in the pharmaceutical industry who is experienced with GMP, GAMP, and GDP. You will have good...

About the RoleWe are seeking a skilled Technical Documentation Specialist to join our team of experts working on two-stroke engines.In this role, you will play a key part in developing and maintaining technical documentation, collaborating closely with your colleagues and other specialists. This includes creating spare parts documentation and after-sales...

The Ubique Systems' IT Compliance Lead will play a critical role in ensuring the Genetics Analysis Platform meets regulatory requirements. This involves developing and executing a validation strategy for the Non-GxP SaaS solution.Responsibilities include creating end-to-end documentation, performing assessments, and writing technical reports. The role...

About the TeamYou will be joining a dynamic team of 13 technical specialists dedicated to delivering high-quality documentation. Our team focuses on digitalisation, ensuring that relevant information is accessible to the right people at the right time.Safety for operational staff and engine reliability are core aspects of our DNA. We collaborate closely with...

Senior/Principal Medical Writing ConsultantsPharma IT is hiring experienced Senior/Principal Medical Writer Consultants to join our Regulatory Affairs & Medical Writing TeamIn this role, you will work as a consultant to support our clients in the Pharma, Biotech and Medical Device industries.In this position, you will work on-site at the client's location or...

Oresund Pharma ApS is seeking a Product Lifecycle Specialist to join our Regulatory department. In this role, you will be responsible for ensuring compliance with regulatory requirements and commercial demands worldwide.As a key member of our team, you will focus on juggling and structuring various tasks, collaborating with both internal and external...

We are Tactile Games Aps, a leading developer of casual puzzle games. Our mission is to create out-of-the-ordinary gaming experiences that captivate audiences worldwide.To achieve this goal, we need talented individuals like you to join our team. As a Technical Writer, you will play a critical role in ensuring that our documentation is accurate, complete,...

Job DescriptionWe are looking for an experienced Information Management Specialist to be part of our dedicated team providing a high standard of data quality and compliance with the Information Management governance.You will play an important role in ensuring that Information Management requirements are implemented in projects, creating and maintaining...

Select how often (in days) to receive an alert:Are you ready to join a dynamic environment with ongoing changes and set your vision for the future? Do you want to be part of creating smarter solutions and forming strategic partnerships? Are you excited about the opportunity to set directions and embark on a new journey?LEO Pharma is seeking a talented...

Technical Documentation Specialist for Two-Stroke EnginesDo you dream of working with technical documentation in a dynamic team where discussions about new engine- and fuel technologies and updates are part of your daily routine? Are you passionate about contributing to a sustainable, carbon-neutral future in the maritime industry? Then we have the right job...

Job SummaryWe are seeking an experienced Medical Dermatology Professional to lead our Global Safety Surveillance team at LEO Pharma. As a key member of our team, you will be responsible for managing and leading a team of Global Safety Advisors and Safety Leads, ensuring compliance with pharmacovigilance processes, regulations, and guidelines.Key...

Select how often (in days) to receive an alert: Senior Corporate Counsel - R&D Legal & HQ Operations Field of work: Legal, Audit & Compliance Posting Date: 10 Mar 2025 Shape the LEO Pharma of tomorrow At LEO Pharma, our mission goes beyond the ordinary. We're on an ambitious journey to become global leaders in medical dermatology.To support this mission we...

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...

Company OverviewLEO Pharma is a global leader in medical dermatology, dedicated to leaving a lasting impact on patients, colleagues, and the planet. Our innovative approach sets us apart, empowering individuals to drive change and make a visible impact.We value diversity and welcome applications from all qualified candidates, recognizing that our different...

Er du en struktureret og detaljeorienteret Space Manager med erfaring inden for koordinering af installationer og pladsforbrug i projektering af nye bygninger? Vil du være en del af et stærkt og innovativt team hos Sweco, hvor du kan bidrage til udviklingen af fremtidens pharma-faciliteter? Så er det dig, vi leder efterPharmaindustrien er en af Danmarks...

Select how often (in days) to receive an alert:Senior Corporate Counsel - R&D Legal & HQ OperationsField of work: Legal, Audit & CompliancePosting Date: 10 Mar 2025Shape the LEO Pharma of tomorrowAt LEO Pharma, our mission goes beyond the ordinary. We're on an ambitious journey to become global leaders in medical dermatology.To support this mission we are...

Job TitleWe are seeking a Senior Case Management Specialist to join our team at LEO Pharma. As a key member of our Global Safety Surveillance team, you will be responsible for managing and leading a team of Global Safety Advisors and Safety Leads, ensuring compliance with pharmacovigilance processes, regulations, and guidelines.ResponsibilitiesDevelop and...