Regulatory Specialist Italy

**Senior Regulatory Affairs Specialist - Medical Device** Xplore Life Science is recruiting for Senior Regulatory Affairs Specialist to join a leading medical device company, that has a global presence. The role is suitable would like to provide and maintain regulatory support, supply regulatory input and data and ensure compliance with...

At Planet Pharma, we are seeking a highly skilled Regulatory Affairs Specialist to join our team.About the RoleWe are looking for a detail-oriented and analytical individual who can assess CMC changes against regulatory filings to ensure compliance. The ideal candidate will have a strong understanding of regulatory requirements and be able to communicate...

**Senior Quality Assurance & Regulatory Specialist**: **Introduction**: A spin-off of one of the world’s largest In-Vitro Diagnostics (IVD) manufacturers, located in Berlin is currently searching for an experienced Quality Assurance & Regulatory Affairs Specialist to join their ever growing team after a successful merger. **This role will offer you**: -...

**Solaris** is a tech company with a full German banking license. Our Banking-as-a-Service platform enables businesses to offer their own financial products. With our straightforward APIs, our partners can access and integrate a wide range of solutions such as digital banking, payments, cards, identification and lending services. As a market leader we are...

As a Senior / Staff Regulatory Affairs Specialist at Stryker, you will be at the heart of groundbreaking advancements, championing the integration of software-based innovative technology in upcoming product launches for our ENT division (Ear, Nose & Throat). This role uniquely caters to individuals with a background in software and/or regulatory affairs,...

Meditrial is a full-service clinical research organization (CRO) dedicated to clinical trial conduct, medical education, regulatory affairs and market access. Our offices are located in Germany, Italy, Switzerland, UK, United States and our teams rely on digital tools to work collaboratively to achieve shared goals. Since 2008, Meditrial delivers...

Meditrial is a full-service clinical research organization (CRO) dedicated to clinical trial conduct, medical education, regulatory affairs and market access. Our offices are located in Germany, Italy, Switzerland, UK, United States and our teams rely on digital tools to work collaboratively to achieve shared goals. Since 2008, Meditrial delivers...

Marketing Influencer RoleThis role involves building and expanding the brand presence in Italy by establishing successful partnerships with key influencers on various platforms.You will take part in identifying, contacting, and negotiating with influencers and agencies to create mutually beneficial collaborations.Assist in planning and executing influencer...

**Description**: The Sr. Regulatory Affairs Specialist works under mínimal supervision supporting cross functional teams with regulatory strategy and execution of Inari devices and modifications focused on countries Outside the United States (OUS), including but not limited to the European Union (EU), United Kingdom (UK), Middle East,...

**Company Overview**: Meditrial is a dynamic and rapidly growing multinational company specializing in providing clinical and regulatory services to medical device companies in the USA and Europe. With a commitment to excellence and innovation, we empower our clients to navigate complex regulatory landscapes and bring life-changing medical devices to market...

**MKS Instruments Deutschland GmbH*** Specialist Regulatory Affairs (f/m/d) - Berlin- Vollzeit- Feste AnstellungMKS in Berlin is looking for a **Specialist Regulatory Affairs (f/m/d)**: In your role as Specialist Regulatory Affairs (f/m/d) at Atotech Deutschland GmbH you are responsible for all aspects of Global Regulatory Affairs such as for the...

Job Description:This role involves developing and maintaining a solid understanding of regulatory requirements and available guidance documents and resources.The Regulatory Affairs Manager assists with planning, scientific writing, and critical reviews of submissions to ensure conformance with regulatory requirements.Excellent communication skills are...

**_Customer Specialist - QM & Regulatory Affairs_**: **_Cherry Ventures is supporting our portfolio with this hire_**: **Summary about the role**: We are looking for a dedicated Quality Management & Regulatory Affairs Customer Specialist with experience in quality and regulatory compliance in MedTech to join our team in Paris, Berlin, or Vienna. This role...

Business Development - Athens, Berlin, Madrid, Rome **About the Role** - As the International Industrial Development Lead for Lockheed Martin, They will be an integral part of the Global Business Development and Strategy across Spain, Italy, Greece, and Germany. Reporting directly to the Director of Global Industrial Partnerships, the role demands a...

LOCATION- Berlin, Hamburg, Kassel, Germany- STARTING DATE- Next possible starting date- CONTRACT TYPE- Permanent- DEPARTMENT- Carbon Management & Hydrogen- WORKING HOURS- Full-time- REFERENCE CODE- 964- What you can expect- What you can expect- What you can expect - text- You work in a dedicated team in a dynamic market environment. The general...

**Your mission**: **About DeepSpin** DeepSpin is a HealthTech startup pursuing the mission to make Magnetic Resonance Imaging universally accessible. Today 7 out of 10 people globally do not have access to this life-saving imaging modality. Through our cutting-edge technology we are going to change that. Backed by globally leading VCs, we are now expanding...

**About DeepSpin** DeepSpin is a HealthTech startup pursuing the mission to make Magnetic Resonance Imaging universally accessible. Today 7 out of 10 people globally do not have access to this life-saving imaging modality. Through our cutting-edge technology we are going to change that. Backed by globally leading VCs, we are now expanding our world-class...

We are seeking a highly skilled Compliance Specialist to join our team at Michael Page. As a key member of our compliance department, you will be responsible for ensuring that our business practices align with regulatory requirements.Key Responsibilities:Develop and implement compliance programs to mitigate risk and ensure regulatory complianceAnalyze and...

**Site**: Berlin**Specialist field**: Regulatory Affairs**Career level**: Experienced professionals**Commencement date**: with immediate effect**Type of contract**: Fixed-term**Working time**: Full-timeWithin our International Regulatory Affairs & Drug Safety Department in Berlin, you will be responsible for the acquisition and regulatory management of...

Company OverviewCherry Ventures is a venture capital firm that supports innovative startups. As a key partner, we help our portfolio companies scale and succeed.SalaryWe offer a competitive salary ranging from €80,000 to €110,000 per annum, depending on experience.Job DescriptionWe are seeking a dedicated Quality Management & Regulatory Affairs Customer...