Head of Regulatory Affairs

Job Description Head of Regulatory Affairs THE COMPANY Our client, a world-leading biotech company, is at the forefront of liquid biopsy technology.They have developed a patent-protected platform that captures rare circulating tumour cells (CTCs) from blood in a minimally invasive manner, pushing the boundaries of cancer diagnostics and personalised...

Head of Regulatory Affairs THE COMPANY Our client, a world-leading biotech company, is at the forefront of liquid biopsy technology.They have developed a patent-protected platform that captures rare circulating tumour cells (CTCs) from blood in a minimally invasive manner, pushing the boundaries of cancer diagnostics and personalised medicine.Their...

Head of Regulatory AffairsTHE COMPANYOur client, a world-leading biotech company, is at the forefront of liquid biopsy technology. They have developed a patent-protected platform that captures rare circulating tumour cells (CTCs) from blood in a minimally invasive manner, pushing the boundaries of cancer diagnostics and personalised medicine. Their...

Job Description Head of Regulatory Affairs THE COMPANY Our client, a world-leading biotech company, is at the forefront of liquid biopsy technology. They have developed a patent-protected platform that captures rare circulating tumour cells (CTCs) from blood in a minimally invasive manner, pushing the boundaries of cancer diagnostics and personalised...

Head of Regulatory Affairs THE COMPANY Our client, a world-leading biotech company, is at the forefront of liquid biopsy technology. They have developed a patent-protected platform that captures rare circulating tumour cells (CTCs) from blood in a minimally invasive manner, pushing the boundaries of cancer diagnostics and personalised medicine. Their...

Job OverviewSingular: Building Brilliant Biotechs seeks an experienced Head of Regulatory Affairs to lead our team in Guildford.This key leadership role involves acting as the Person Responsible for Regulatory Compliance (PRRC) for MDR/IVDR, ensuring compliance with international medical device directives and regulations worldwide.The ideal candidate will...

Job OverviewSingular: Building Brilliant Biotechs is a world-leading biotech company at the forefront of liquid biopsy technology. Our patented platform captures rare circulating tumour cells (CTCs) from blood in a minimally invasive manner, pushing the boundaries of cancer diagnostics and personalised medicine.We are seeking an experienced Regulatory...

About the RoleWe are seeking an experienced Head of Regulatory Affairs to join Singular: Building Brilliant Biotechs' team in Guildford. As a key leadership figure, you will oversee regulatory compliance for MDR/IVDR, ensuring the organisation meets all relevant standards across global markets. You will provide strategic direction and operational oversight...

Singular: Building Brilliant BiotechsJob Title:Head of Regulatory AffairsAbout the RoleWe are seeking an experienced Compliance Leader - Medical Devices to join our team in Guildford. This key leadership role involves acting as the Person Responsible for Regulatory Compliance (PRRC) for MDR/IVDR, ensuring the organisation meets all relevant regulatory...

Head of Regulatory Affairs Our client, a world-leading biotech company, is at the forefront of liquid biopsy technology. They have developed a patent-protected platform that captures rare circulating tumour cells (CTCs) from blood in a minimally invasive manner, pushing the boundaries of cancer diagnostics and personalised medicine. Their groundbreaking...

Singular: Building Brilliant Biotechs is seeking a Regulatory Affairs Leader to drive compliance and ensure the success of their innovative cancer diagnostic technology.This role involves providing expert guidance on regulatory requirements and ensuring the organisation meets all relevant standards.The ideal candidate will have a strong background in IVD...

Job OverviewSingular, a pioneer in building brilliant biotechs, seeks an experienced Regulatory Affairs Expert to spearhead regulatory compliance across global markets.Estimated Salary: £80,000 - £110,000 per annumAbout the RoleThis key leadership position requires expertise in IVD medical device product development, adhering to standards such as ISO14971....

Opportunity OverviewWe are seeking a seasoned Regulatory Affairs Director to lead our team in Guildford. In this key role, you will be responsible for ensuring our organisation meets all relevant regulatory standards across global markets.This position requires strategic leadership and operational oversight to manage compliance with international medical...

Role SummaryWe are looking for a seasoned regulatory professional to join our team in Guildford.As the Head of Regulatory Affairs, you will provide strategic direction and operational oversight to the regulatory and quality teams.Your expertise in global medical device directives, including FDA regulations, MEDDEV guidelines, and ISO standards, is essential...

As a Biotech Regulatory Affairs Leader at Singular: Building Brilliant Biotechs, you will play a pivotal role in shaping the regulatory strategy for our cutting-edge cancer diagnostic technology. Your expertise in IVD medical device product development, adhering to standards such as ISO14971, will be instrumental in ensuring compliance with international...

About the Job:We are seeking an experienced Regulatory Affairs Director to join our team in Guildford.This key leadership role will act as the Person Responsible for Regulatory Compliance (PRRC) for MDR/IVDR, ensuring the organisation meets all relevant regulatory standards across global markets.The successful candidate will provide strategic direction and...

About the OpportunitySingular: Building Brilliant Biotechs is seeking an experienced Head of Regulatory Affairs to join its team in Guildford. As a key member of the team, you will be responsible for ensuring the organisation meets all relevant regulatory standards across global markets. You will provide strategic direction and operational oversight to the...

Job Title: Pharmacovigilance and Scientific Information ManagerWe are seeking a highly skilled Pharmacovigilance and Scientific Information Manager to join our team at Zentiva Poland.About the Role:This is an exciting opportunity for a seasoned professional with experience in pharmacovigilance and scientific information management. As a Pharmacovigilance and...

Key ResponsibilitiesThe successful Head of Regulatory Affairs will be responsible for defining regulatory strategies, guiding clinical and analytical validation studies, and liaising with regulatory authorities. This position offers the opportunity to influence the global commercial rollout of a revolutionary cancer diagnostic technology. You will play an...

Cancer Diagnostic Innovation LeaderThe successful candidate will act as Person Responsible for Regulatory Compliance (PRRC) for MDR/IVDR, ensuring the organisation meets all relevant regulatory standards across global markets. They will provide strategic direction and operational oversight to the regulatory and quality teams, managing compliance with...