Regulatory Affairs Specialist

We are seeking a talented Regulatory Affairs Specialist to join our client's regulatory team in support of the expansion of their ISO 13485 diagnostics product pipeline. Reporting to the Regulatory Affairs Manager, you will play a crucial role in ensuring regulatory compliance and supporting the successful submission of our products to global regulatory...

As Regulatory Affairs Specialist responsibilities include: - Collaborate closely with the Regulatory Affairs Manager to develop and maintain technical files and submissions for global regulators. - Utilise your regulatory expertise to support the development of regulatory strategies for product submissions. - Analyse routes to market and provide relevant...

We are seeking a talented Regulatory Affairs Specialist to join our client's regulatory team in support of the expansion of their ISO 13485 diagnostics product pipeline. Reporting to the Regulatory Affairs Manager, you will play a crucial role in ensuring regulatory compliance and supporting the successful submission of our products to global regulatory...

**About Mirada Medical...** Mirada Medical develops medical imaging and cancer treatment planning solutions that provide simple and accessible solutions to complex image analysis problems in the diagnosis and treatment of cancer and other diseases. Our solutions interoperate with other IT systems in the healthcare enterprise, such as EHRs and PACS,...

About Us Oxford Nanopore Technologies is headquartered at the Oxford Science Park outside Oxford, UK, with satellite offices and commercial presence in many global locations across the US, APAC and Europe. Oxford Nanopore employs from multiple subject areas including nanopore science, molecular biology and applications, informatics, engineering, electronics,...

Senior Regulatory Affairs Specialist About the role The Regulatory Affairs Specialist liaises with the Regulatory Affairs and Quality teams, R&D and Product Management to provide regulatory input into NPI Project Core teams and company operations. They assist in the preparation and submission of regulatory applications and registrations as assigned...

Regulatory Specialist (REMOTE or On-site) page is loaded Regulatory Specialist (REMOTE or On-site) Apply locations Oxford, UK - Oxford Immunotec time type Full time posted on Posted 3 Days Ago job requisition id JR-038611 Job Title Regulatory Specialist (REMOTE or On-site) Revvity is a developer and provider of end-to-end solutions designed to...

TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives. Quality and Regulatory Specialist As the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver...

TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives.Quality and Regulatory SpecialistAs the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver groundbreaking...

TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives.Quality and Regulatory SpecialistAs the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver groundbreaking...

TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives. Quality and Regulatory Specialist As the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver...

TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives. Quality and Regulatory Specialist As the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver...

TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives. Quality and Regulatory Specialist As the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver...

TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives.Quality and Regulatory SpecialistAs the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver groundbreaking...

TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives. Quality and Regulatory Specialist As the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver...

TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives. Quality and Regulatory Specialist As the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver...

LennTech Search are working with an innovative software medical device company whom have a need for an experienced Regulatory Affairs Manager. Main Duties Lead company regulatory submissions to the FDA. Preparation of full 510(k) Q-Submissions. Prepare and submit applications and reports to applicable regulatory agencies. Respond to reviews and...

LennTech Search are working with an innovative software medical device company whom have a need for an experienced Regulatory Affairs Manager. Main Duties Lead company regulatory submissions to the FDA. Preparation of full 510(k) Q-Submissions. Prepare and submit applications and reports to applicable regulatory agencies. Respond to reviews and...

Job Overview: Regulatory Specialist Company: Oxford Immunotec Location: Abingdon, UK Position Type: Fixed-Term, 9 months Work Arrangement: On-site OR REMOTE! Company Overview: Oxford Immunotec, a Revvity company is a leading global diagnostics company dedicated to bringing energy and innovation to the field of diagnostic testing. We offer regulated...

Job Title: Senior Regulatory Affairs and Clinical Lead Job Type: Full time, permanent position Location: West Oxfordshire, (On-site) Remuneration: £100,000 + This is an excellent opportunity to join a leading medical device manufacturing that is the world leader in Glucose Monitoring, their ranging product portfolio, develops and manufactures glucose...