Medical Device Regulatory

Lead and manage regulatory affairs and quality assurance activities to support the design development manufacturing and distribution of medical devices. · Ensure compliance with FDA and global regulations · SUPPORT REGULATORY SUBMISSIONS CONDUCT AUDITS AND LEAD CONTINUOUS IMPROVE ...

The Director, Device, Global Regulatory Affairs is responsible for developing and leading global regulatory strategies for the device component of drug-device combination products. · ...

TFS HealthScience is a leading global Contract Research Organization (CRO) providing clinical development and regulatory services to pharmaceutical, biotechnology, and medical device companies. · We are seeking a highly experienced Freelance Director, Regulatory Affairs – Device ...

We are seeking an experienced medical devices regulatory affairs professional to develop and execute regulatory strategies and manage product submissions for novel hardware and software as a medical device (SaMD) products for distribution into worldwide markets. · This role is wi ...

Shape the future of medicine by accelerating drug discovery and development to find answers for patients and their families. · Serve as GRA Device Lead on assigned project teams. · Provide regulatory guidance and advice to Global Regulatory Team (GRT) and cross-functional teams. ...

The Global Regulatory Affairs Device Lead will drive global regulatory strategies for medical device and combination products.We are seeking an experienced Regulatory Affairs professional with familiarity with international submissions from within a global healthcare organization ...

We are looking to fill a Regulatory Affairs Professional Medical Devices & (f|m|d) position in Göttingen. The role involves preparing and executing clinical and performance data documents, as well as post-market surveillance documents. · The job is full-time and can be performed ...

We are seeking an experienced medical devices regulatory affairs professional to develop and execute regulatory strategies and manage product submissions for novel hardware and software as a medical device (SaMD) products for distribution into worldwide markets. · Act as the core ...

Regulatory Affairs Specialist- Medical Devices role at Sunstar Americas, Inc. involves supporting the preparation of regulatory 510(k) submissions and assisting international business partners with product registrations. · BS in Science or Medical / Healthcare related field or hi ...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medic ...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medic ...

TFS HealthScience is seeking a Freelance Director, Regulatory Affairs – Device Expert to support its growing medical device and combination product portfolio. · Support USA/FDA IND (Investigational New Drug) and IDE (Investigational Device Exemption) submissions. · ...

We are adding a driven, · detail-oriented Regulatory Affairs Specialist to our expanding medical device team to handle regulatory submissions, · compliance activities and product lifecycle management for implantable cardiovascular devices.Support regulatory pathways for new produ ...

Oracle's Healthcare and Life Sciences business is a global leader in industry-specific software and solutions to healthcare providers, At a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate,, The success of ...

We are seeking a Regulatory Specialist to join our team at Sunstar Americas Inc.As a Regulatory Specialist you will be responsible for supporting the preparation of regulatory submissions and assisting international business partners with product registrations. · ...

TFS HealthScience is seeking a Freelance Director for Regulatory Affairs – Device Expert to support medical device and combination product portfolio. · ...

At a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate... · ...

Join us and become part of our global team at Sunstar Americas Inc., where together we can achieve success and contribute to a better future. We are seeking a Regulatory Affairs Specialist- Medical Device with experience in the US and Canada regulated industry. · ...

The success of large global health companies requires regulatory leaders who can navigate laws and regulations across the globe. · ...

We are looking for regulatory affairs experts in the med-tech space to play a key role in driving Oracle's success and competitiveness in the healthcare and life sciences sector. · ...