Safety and 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...

About the DepartmentThe QPPV Office is an area within Global Patient Safety, located in Novo Nordisk headquarters in Denmark. We are responsible for handling adverse events and monitoring patient safety globally. Our team consists of different departments, each responsible for various aspects of PV system oversight and support, as well as performance...

Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Do you want to lead and drive safety surveillance activities in development projects in rare diseases? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark? Then, this might be a great opportunity for you...

Job OverviewWe are seeking an experienced safety surveillance specialist to join our team at Novo Nordisk. As a key member of our Global Safety team, you will be responsible for leading safety surveillance activities in development projects for rare diseases.Your primary focus will be on ensuring the safe development and marketing of our products, working...

Job DescriptionWe are seeking a highly skilled Health Safety Manager to join our dynamic team in Corporate Facilities. As a key advisor to management, you will be responsible for driving the H&S agenda and ensuring that our current setup meets both requirements and ambitions on H&S.Your responsibilities will include:Providing advice and support to management...

Job OverviewWe are seeking a skilled professional to join our Plant Engineering team as a Compliance Engineer. In this role, you will work closely with colleagues and stakeholders to maintain compliance levels and handle quality-related tasks.About UsAGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization...

Our ValuesWe value collaboration, open dialogue, and a sense of shared and individual responsibilities. Our flat hierarchy ensures that everyone has a voice and is empowered to take ownership of their work.We believe in the power of diversity and inclusion, and we strive to create an environment where everyone feels valued and respected.About the JobThis is...

About the PositionThis role requires a highly skilled professional with experience in safety surveillance and development in the pharmaceutical industry. You will be responsible for leading safety surveillance activities in development projects for rare diseases and working closely with other teams to ensure safe product development and marketing.As a senior...

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...

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 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...

We are looking for a highly motivated and experienced Regulatory Affairs professional to join our team as a Senior Regulatory Affairs Specialist. In this role, you will be responsible for ensuring regulatory compliance and securing approvals for new products, line extensions, and additional claims, while supporting business objectives.The ideal candidate...

We are seeking an Automation Engineer to join our team and drive innovation in aseptic manufacturing. As an Automation Engineer, you'll work closely with pilot sites and facilitate the integration of new projects across other parts of the organization.About the Role:The position involves creating innovative automated solutions and securing the successful...

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 —...

Jobbeskrivelse Placering Bagsværd, Denmark Jobkategori Quality Ansøg nu Would you like to play an important role in ensuring the quality and safety of products for clinical trials, where you can use your solid QA and validation experience in a project context? Then we can offer you a unique position with a lot of responsibility and impact in a dynamic...

Manager, Quality & Compliance Monitoring, QPPV Office Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Do you want to play a key role in driving the pharmacovigilance strategy and optimizing the Pharmacovigilance processes and activities? Would you like to be part of one of the most skilled and advanced...

About the PositionWe are seeking a highly skilled and experienced QA Specialist to lead 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...

About the RoleWe are seeking a highly skilled Quality Assurance Specialist to join our QC Stability Team. The successful candidate will be responsible for ensuring the stability of Drug Substance, Drug Product, Placebo, and Reference Material.Key Responsibilities:Develop and implement stability protocols and reportsCollaborate with stakeholders on analytical...

As a key member of the Novo Nordisk PSQIT organisation, you will be part of Chemistry, Manufacturing and Control (CMC) Development & Scaling. Our team makes a real difference for patients with chronic diseases across the world by developing, manufacturing and distributing drug candidates for clinical trials.We are looking for an Automation Systems Specialist...

Jobbeskrivelse Placering Bagsværd, Denmark Jobkategori Engineering & Technical Do you thrive in developing innovative solutions to complex Health & Safety (H&S) challenges? Are you excited by the prospect of working on challenging H&S projects in a dynamic business environment like Corporate Facilities? Are you motivated by partnering with stakeholders...