Regulatory Affairs Professional

Supports worldwide product registrations by providing information and documents to Siemens Regional Unit (RU) in Asia-Pacific, Middle East Asia, South and Latin America and Europe. - o Provides answers to technical questions from Siemens Regional Unit (RU) and international regulatory authorities. - o Prepares and/or compiles technical documents for the...

o Supports worldwide product registrations by providing information and documents to Siemens Regional Unit (RU) in Asia-Pacific, Middle East Asia, South and Latin America and Europe. - o Provides answers to technical questions from Siemens Regional Unit (RU) and international regulatory authorities. - o Prepares and/or compiles technical documents for the...

ce: 5-8 yrs **Qualifications**: You have successfully completed a course of studies in a technical or clinical field, preferably in engineering, medicine, medical engineering or (medical) informatics You can offer extensive professional experience in regulatory affairs for Software as Medical Device, SaaS, and/or cloud deployments You have a sound knowledge...

RAQA (Regulatory Affairs Quality Assurance) professional is responsible for implementation of process across the assigned projects, - Process facilitation to project teams from Initiation till Release of the project - Conduct audit to identify process gaps in the project - Review the project deliverables and provide feedback to project teams - Improve...

Job Title: Regulatory Affairs ManagerDepartment: Regulatory Affairs / Quality & ComplianceReporting to: Head Regulatory AffairsJob Purpose:To lead and oversee all regulatory affairs activities, ensuring company products comply with applicable local and international regulatory requirements. The role involves developing regulatory strategies, managing...

Job Title: Regulatory Affairs Associate – Authoring.  Role detailed classification Regulatory Affairs Authoring Job Summary: We are seeking highly skilled and experienced Life Sciences (LS) Regulatory Affairs (RA) Associate – Authoring to join our LS Practice team. The successful candidate will be responsible for LS Regulatory Authoring and/or other...

Job Description Job Title: Regulatory Affairs Associate – Authoring.  Role detailed classification Regulatory Affairs Authoring Job Summary: We are seeking highly skilled and experienced Life Sciences (LS) Regulatory Affairs (RA) Associate – Authoring to join our LS Practice team. The successful candidate will be responsible for LS Regulatory Authoring...

**Department**:RA CMC Biotech and Rare Disease **About the department** Regulatory Affairs plays an important role in ensuring all Novo Nordisk Medicines and Devices developed with compliance and keeping patients in mind. Liaising between relevant authorities and Novo Nordisk stakeholders, Regulatory Affairs will be involved throughout phases of product...

**Department: International Operations Regulatory Affairs** **About the department** International Operations Regulatory Affairs Bangalore in Global Regulatory Affairs Global Business Services (GBS) is a global RA hub consisting of high calibre regulatory professionals. The objective of the team is to offer core RA competencies enabling NN secure fast,...

 What do we offer you? Competitive salary and benefits packageRemote work opportunitiesProfessional development and growth opportunitiesCollaborative and supportive team environmentChance to make a significant impact on a global scaleWork-life balance Who are you?We are looking for a dedicated and experienced Regulatory Affairs Specialist to join our...