Senior Regulatory Affairs Specialist - Wollerau

We are looking for a Regulatory Affairs Specialist who plays a key part in safeguarding compliance across global markets. · Provide regulatory compliance support to customers to ensure outstanding customer experience · Ensure compliance of the company's product range with applica ...

We are looking for a Regulatory Affairs Specialist who plays a key part in safeguarding compliance across global markets with a strong emphasis on European chemical legislation. · Your expertise will help ensure that our products meet stringent regulatory standards while supporti ...

We are looking for a Regulatory Affairs Specialist who plays a key part in safeguarding compliance across global markets with a strong emphasis on European chemical legislation. · Provide regulatory compliance support to customers to ensure outstanding customer experience. · Ensu ...

We are seeking a new team member for our Vascular Intervention (VI) regulatory affairs group. · The regulatory affairs department is responsible for worldwide registration of the newly developed class II and III innovative products and the existing portfolio · ...

This role will support product registrations in low-effort countries and maintain regulatory documentation up to date for global registrations. · ...

+Job summary · This role will be located at the Bulach, Switzerland location which is responsible for the development, production and marketing of balloon catheters and drug-coated stent systems. · +University degree in natural sciences, pharmacy, pharmacology, medicine or engine ...

To optimize our tools for clinical value we take a disease-centric approach addressing large unmet need for more efficient visual field testing in glaucoma patients. · We combine AI algorithms virtual reality cloud computing build next generation systems test visual function. · ...

As a QA & Regulatory Specialist at PeriVision you will ensure quality safety and regulatory compliance of our software-based medical solution. · Support the planning implementation and maintenance of the Quality Management System (QMS) · Collaborate with software engineers to def ...

Senior Global Medical Advisor at Octapharma in Lachen. Responsible for project management of NIS and IIS. · ...

We are a privately-owned company where the warmth of family meets the scale of a global organisation.Join us in shaping our vision to provide new health solutions advancing human life. · Responsible for project management of NIS and IIS · Manage the publication processes related ...

Become part of a vital chain and contribute to our common goal of making people's lives better. · ...

We are seeking a Senior Global Medical Advisor to join our team. As a key scientific and clinical expert, you will bridge the gap between clinical practice and pharmaceutical development. · Project management of NIS and IIS · Publishing processes related to clinical studies cond ...

Become part of a vital chain and contribute to our common goal of making people's lives better. · ...

We are looking for a Medical Information Specialist who is energized by science, driven by purpose, and inspired by collaboration. · ...

Johnson & Johnson believes health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured. · ...

The EU CTR Submission Specialist is responsible for planning, preparing, managing, and maintaining regulatory submissions for clinical trials in compliance with EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials Information System (CTIS). This role covers the ...

The EU CTR Submission Specialist is responsible for planning and managing regulatory submissions for clinical trials in compliance with the EU Clinical Trial Regulation via the Clinical Trials Information System. · ...

The EU CTR Submission Specialist is responsible for planning and managing regulatory submissions for clinical trials in compliance with EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials Information System (CTIS). · This role covers the entire lifecycle of a ...

The EU-CTR Submissions Group Lead is a critical leadership role overseeing operational activities related to end-to-end trial submissions and lifecycle management under the EU Clinical Trials Regulation (EU CTR 536/2014). · ...

We are looking for a Medical Information Specialist who is energized by science, driven by purpose, and inspired by collaboration. If you thrive in a dynamic environment where curiosity and compassion meet scientific excellence, this role is for you. · ...