Regulatory Compliance Expert

Job Title: Compliance Documentation Expert">We are looking for a Compliance Documentation Expert to join our team at AGC Biologics. As a Compliance Documentation Expert, you will be responsible for creating and maintaining high-quality documentation to support our compliance with regulatory requirements and industry standards.Key Responsibilities:Create and...

Reckitt Benckiser is a global leader in hygiene, health, and nutrition products. Our purpose drives our actions: to protect, heal, and nurture people around the world.About the RoleWe are seeking a highly skilled Regulatory Affairs Associate to join our team in Hygiene. As a key member of our regulatory team, you will be responsible for ensuring compliance...

The RoleWe are seeking an experienced Sterilization and Microbiology Expert to join our Quality Control team. In this role, you will be responsible for ensuring the highest standards of quality and safety in our products, from raw materials to finished goods. Your expertise in sterilization and microbiology will play a critical role in maintaining our...

About the Job">We are seeking a highly motivated and detail-oriented Regulatory Compliance Specialist to join our team at AGC Biologics. In this role, you will be responsible for ensuring compliance with regulatory requirements and industry standards in the pharmaceutical industry.Key Responsibilities:Cooperate with colleagues within the department and...

Navigating Complex Regulations to Drive Business SuccessIn this dynamic role, you will leverage your expertise in regulatory affairs to drive business growth and expansion while ensuring compliance with product safety standards and regulatory requirements in Nordic markets. As a Regulatory Affairs Associate in our Hygiene division, you will develop and...

About the Role\This exciting opportunity is part of Novo Nordisk's Global Regulatory Affairs team. As a Regulatory Specialist, you will play a key role in shaping the company's regulatory strategies and ensuring compliance with regulatory requirements.\Key Responsibilities:\\Develop and implement effective regulatory strategies to support the development and...

Select how often (in days) to receive an alert: Create Alert Expert in Regulatory Affairs - Primary Packaging Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Are you ready to take on new challenges in primary packaging development across emerging therapeutic areas and innovative products? Would you like to...

At Novo Nordisk A/S, we are seeking a highly skilled Regulatory Affairs Professional to join our team. This role will play a key connection between scientists and Health Authority regulators, ensuring fast and successful regulatory submissions and approvals in all global markets.About the RoleThis is an exciting opportunity for a talented individual to join...

Job OverviewOur CMC API QA department employs 35 skilled and motivated colleagues in four teams, all based in Denmark.We work with assuring quality and compliance of the CMC API facilities, equipment, quality management system, materials, and the release of API for clinical trials.Key qualifications for the role include:MSc in Pharmaceutical Sciences,...

Job Description\Novo Nordisk A/S is seeking an experienced Regulatory Affairs Specialist to join our team. The ideal candidate will have a strong background in regulatory affairs and be able to drive the strategic direction of innovative development projects.\Main Responsibilities:\\Execute and drive the regulatory strategy to obtain approvals\Provide...

Department Overview\The RA Rare Bleeding Disorders department at Novo Nordisk is a dynamic and innovative team that contributes to the development of different products and projects within Rare Bleeding Disorders.\Main Responsibilities:\\Contribute to the development of regulatory strategies and plans for rare bleeding disorders projects\Collaborate with...

About the Department:You will be joining the Quality Assurance department, consisting of over 80 colleagues, with primary responsibilities in Manufacturing, Raw Materials, Quality Control, and Facilities and Equipment. Our main objective is to ensure that our production facilities and laboratories comply with current Good Manufacturing Practice (GMP)...

Fusion Consulting seeks a skilled professional to support the implementation of an ERP solution for Local/Regional Manufacturing and Affiliate. This role involves working closely with an international team and the supplier to ensure configuration management, technical design documentation, and installation verification processes meet compliance and...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in innovative development within rare diseases.This is an exciting opportunity to become part of a fast-changing field where no two days are alike.The PositionAs a Regulatory Specialist, you will be responsible for setting the regulatory strategic direction in...

Are you looking for a challenging role that combines data governance, compliance, and quality assurance? Do you want to make a meaningful contribution to the success of a leading global healthcare company like Novo Nordisk A/S?We are seeking a highly motivated and experienced Quality & Compliance Partner to join our R&D Data Governance Office. In this role,...

Job Title: Global Regulatory Lead in CVD/CKD Area - Strategic ExpertWe are seeking a highly skilled and experienced professional to join our team as a Global Regulatory Lead. As a key member of our cross-functional project teams, you will be responsible for driving regulatory strategies and executing various regulatory tasks.The successful candidate will...

At Novo Nordisk A/S, we are expanding our product and project pipeline in a fast-paced, dynamic environment.We are seeking an engaged Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic small molecules to join the Synthetics & Cell Technologies Department in the RA CMC Biotech & Rare Disease area.The ideal...

City: SoborgWe are Reckitt 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...

As a Data Steward at Novo Nordisk, you will be part of the growth of our processes in digital transformation and bring our new products to our patients faster. You will be responsible for implementing and supporting our data strategy in the Regulatory organisation, ensuring alignment with digital transformation efforts.The ideal candidate will have a strong...

We are seeking a Risk and Compliance Specialist to identify and mitigate risks associated with quality management. The ideal candidate will have experience with risk assessments, quality management systems, and regulatory compliance. Additionally, they will possess strong analytical and problem-solving skills, as well as excellent communication and...