Regulatory Affairs Specialist

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,...

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...

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...

Overview We are looking for a Senior Regulatory Specialist to join our team at Oxford Immunotec, part of the Revvity family to be responsible for the supervision and conduct of Global Regulatory activities. This is a Hybrid role based in Abingdon, Oxford. Responsibilities: Overall responsibilities: To assist the Head of Regulatory Affairs with the...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who...

Oxford Nanopore Technologies is headquartered at the Oxford Science Park outside Oxford, UK, with satellite offices and a 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,...

Are you ready to make a meaningful impact in the diagnostics industry? We're seeking a dedicated individual to join our client's team as a Post-Market Surveillance Coordinator. Reporting to the Regulatory Affairs Manager, you'll take on the crucial responsibility of coordinating all required post-market activities, ensuring compliance with regulatory...

Are you ready to make a meaningful impact in the diagnostics industry? We're seeking a dedicated individual to join our client's team as a Post-Market Surveillance Coordinator. Reporting to the Regulatory Affairs Manager, you'll take on the crucial responsibility of coordinating all required post-market activities, ensuring compliance with regulatory...

Are you ready to make a meaningful impact in the diagnostics industry? We're seeking a dedicated individual to join our client's team as a Post-Market Surveillance Coordinator. Reporting to the Regulatory Affairs Manager, you'll take on the crucial responsibility of coordinating all required post-market activities, ensuring compliance with regulatory...

LennTech Search are working with an innovative software medical device company whom have a need for an experienced Regulatory Affairs Manager. Lead company regulatory submissions to the FDA. Prepare and submit applications and reports to applicable regulatory agencies. Respond to reviews and requests for information from regulatory bodies. Lead...

Are you ready to make a meaningful impact in the diagnostics industry? We're seeking a dedicated individual to join our client's team as a Post-Market Surveillance Coordinator. Reporting to the Regulatory Affairs Manager, you'll take on the crucial responsibility of coordinating all required post-market activities, ensuring compliance with regulatory...

Other responsibilities as Quality Assurance Specialist include: - Provide support to new product development activities and processes - Review and approve Design and Development documentation - Review and approve Change Control documentation for Quality Assurance - Support the maintenance of Quality System documentation - Analyse and communicate proposed,...

Are you ready to make a meaningful impact in the diagnostics industry? We're seeking a dedicated individual to join our client's team as a Post-Market Surveillance Coordinator. Reporting to the Regulatory Affairs Manager, you'll take on the crucial responsibility of coordinating all required post-market activities, ensuring compliance with...

Are you ready to make a meaningful impact in the diagnostics industry? We're seeking a dedicated individual to join our client's team as a Post-Market Surveillance Coordinator. Reporting to the Regulatory Affairs Manager, you'll take on the crucial responsibility of coordinating all required post-market activities, ensuring compliance with...

Are you ready to make a meaningful impact in the diagnostics industry? We're seeking a dedicated individual to join our client's team as a Post-Market Surveillance Coordinator. Reporting to the Regulatory Affairs Manager, you'll take on the crucial responsibility of coordinating all required post-market activities, ensuring compliance with...

Are you ready to make a meaningful impact in the diagnostics industry? We're seeking a dedicated individual to join our client's team as a Post-Market Surveillance Coordinator. Reporting to the Regulatory Affairs Manager, you'll take on the crucial responsibility of coordinating all required post-market activities, ensuring compliance with...

Job Title: Quality SpecialistIf the following job requirements and experience match your skills, please ensure you apply promptly.Location: Oxford (On-Site)Company Overview:CM Medical have partnered with a pioneering wearable device start-up based in Oxford. We're transforming healthcare with innovative solutions empowering individuals and their health. Our...

Job Title: Quality SpecialistLocation: Oxford (On-Site)Company Overview: CM Medical have partnered with a pioneering wearable device start-up based in Oxford. We're transforming healthcare with innovative solutions empowering individuals and their health. Our client are seeking a Quality Specialist to ensure the quality and compliance of our...

As QMS Manager, you will be instrumental in ensuring the effective implementation and maintenance of the Quality Management System across the organisation. You will oversee all aspects of quality management, ensuring compliance with relevant regulations and standards.Key skills and experience:Bachelor's degree in a relevant field (Engineering, Quality...

As QMS Manager, you will be instrumental in ensuring the effective implementation and maintenance of the Quality Management System across the organisation. You will oversee all aspects of quality management, ensuring compliance with relevant regulations and standards. Key skills and experience: Bachelor's degree in a relevant field (Engineering,...