Regulatory Affairs and Quality Assurance Specialist

Job Title: Regulatory Affairs and Quality Assurance SpecialistJob Description:We are seeking a highly skilled Regulatory Affairs and Quality Assurance Specialist to join our team at Newton Colmore Consulting Ltd. As a key member of our medical devices team, you will be responsible for providing quality assurance and regulatory affairs advice on the creation...

Job Title: Regulatory Affairs and Quality Assurance SpecialistWe are seeking a highly skilled Regulatory Affairs and Quality Assurance Specialist to join our team at Newton Colmore Consulting Ltd. As a key member of our team, you will be responsible for providing quality assurance and regulatory affairs advice on the creation of new products and the...

At Hologic, Inc., we are seeking a highly skilled Regulatory Affairs and Quality Assurance Specialist to join our team. As a leading innovator of women's health, we empower people to live healthier lives everywhere, every day.Our quality and regulatory affairs team is responsible for staying up-to-date on new, changing, and existing regulatory requirements....

About the RoleWe are seeking a highly skilled Regulatory Affairs and Quality Assurance Professional to join our team at Newton Colmore Consulting Ltd. As a key member of our medical devices recruitment team, you will be responsible for providing quality assurance and regulatory affairs advice to our clients.The ideal candidate will have a strong background...

Job SummaryWe are seeking a skilled Regulatory Affairs Specialist to join our team at Vectura Group. As a key member of our regulatory affairs department, you will play a crucial role in ensuring compliance with global regulations and guidelines for medical devices and drug-device combination products.Key Responsibilities:Lead regulatory activities across...

VCLS is seeking a highly skilled Regulatory Affairs Specialist to drive forward regulatory processes, ensure compliance, and contribute to innovative clinical trials. The ideal candidate will have 4+ years of experience in Regulatory Affairs, with a focus on Clinical Trial Submissions (CTS). They will possess a deep understanding of regional and local...

Regulatory Affairs SpecialistWe are expanding our Clinical Trial Submissions (CTS) group and are seeking an experienced Regulatory Affairs professional to join our team. This role is ideal for someone with 4+ years of experience in regulatory affairs and a strong background in Clinical Trial Submissions. You'll have the opportunity to work under a generous,...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at ProductLife Group. As a key member of our Regulatory Affairs team, you will be responsible for developing and implementing regulatory strategies to ensure compliance with UK and EU regulations.Key ResponsibilitiesProvide guidance and support to clients on...

Job Title: Quality Assurance SpecialistAbout the Role:We are seeking a highly skilled Quality Assurance Specialist to join our team at Newton Colmore Consulting Ltd. As a Quality Assurance Specialist, you will be responsible for assisting in the development of the QMS system for ISO 13485 standards.Key Responsibilities:Creating and managing technical files...

Regulatory LeadershipVectura Group, a global leader in inhaled therapies and drug-device combination products, seeks a seasoned Regulatory Affairs Manager to drive the success of our medical device and DDCP regulatory activities.Regulatory Expertise: Lead regulatory activities across Vectura Group, specializing in medical devices and DDCPs, to support...

Reed Scientific, a leading partner in the biotech industry, is seeking an experienced Regulatory Affairs Specialist to join their team. This exciting opportunity will see you play a crucial role in ensuring the quality and regulatory compliance of innovative medical devices.  About the Role:This key position will require you to maintain and improve robust...

We are seeking an experienced Regulatory Affairs Specialist to join our team at Vertex Ventures HC. In this role, you will play a critical part in ensuring the regulatory compliance of our cancer therapies.As a key member of our Regulatory Affairs team, you will be responsible for developing and executing global regulatory strategies for assigned programs or...

Senior Regulatory Scientist (Clinical Trial Submissions)We are expanding our Clinical Trial Submissions (CTS) group and are seeking an experienced Regulatory Affairs professional to support our team. This role is ideal for someone with 4+ years of experience in regulatory affairs and a strong background in Clinical Trial Submissions.As part of a supportive...

Role Overview:We are seeking a highly skilled Regulatory Affairs professional to join our Clinical Trial Submissions (CTS) group at VCLS. This role is ideal for someone with 4+ years of experience in regulatory affairs and a strong background in Clinical Trial Submissions.As part of a supportive and collaborative team, you'll play a key role in driving...

Job SummaryWe are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team at Philips International. In this role, you will be responsible for developing and executing the regulatory strategy for new product development, design changes, and field safety corrections for US, EU, and RoW.Your Key Responsibilities:Develop and execute...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Director to join our team at CTI Clinical Trial and Consulting Services. As an Associate Director, Regulatory Affairs, you will play a critical role in developing and delivering innovative global regulatory strategies for our sonelokimab lead indication(s).Key Responsibilities:Develop and...

Job OverviewWe are seeking a highly skilled Senior Associate, Regulatory Affairs to join our team at Bicycle Therapeutics. As a key member of our regulatory affairs department, you will be responsible for the development, execution, and tracking of global regulatory submissions for assigned programs or projects.

Role Overview:We are seeking an experienced Regulatory Affairs professional to join our Clinical Trial Submissions (CTS) group. As a key member of our team, you will play a pivotal role in driving forward regulatory processes, ensuring compliance, and contributing to innovative clinical trials.Key Responsibilities:Identify and coordinate international,...

Job Description: We are seeking a Quality Assurance Specialist to assist in the development of our QMS system for ISO 13485 standards.This role involves creating and managing technical files for several Medical Devices lines, including Class I, Class IIa and Class IIb Medical Devices.You will collaborate with Medical Devices experts and be responsible for...

Associate Director, Regulatory AffairsCpl Life Sciences is seeking an experienced Associate Director, Regulatory Affairs to join our team. This is a permanent, full-time opportunity based in Cambridge, UK, with a hybrid/remote work arrangement.About the RoleWe are looking for a highly skilled and motivated individual to lead our regulatory affairs strategy...