Latest Quality Assurance (MedTech) Jobs

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Sheffield

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Liverpool

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Nottingham

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Manchester

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Newcastle upon Tyne

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

London

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Birmingham

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Leeds

Regulatory Affairs Manager

Regulatory Manager / Medical Devices (UK, Hybrid) This one’s for the regulatory people who actually enjoy being close to the product. I’m working with a UK-based medtech company building a connected medical device that’s already in use and heading into its next regulatory phase. They’re looking for a Regulatory Manager...

CAPU Search

Cambridge

Regulatory Affairs Specialist - ID45000 - Up to £60k DOE

Ready to lead global regulatory strategy? Want to shape compliance for innovative medical technologies? Looking for flexibility, ownership, and international impact? A forward-thinking medical device company is seeking a Regulatory Affairs Manager to join its Quality and Compliance function, playing a pivotal role in managing global regulatory approvals across both...

Humand Talent

Oxfordshire

Vice President Regulatory Affairs

We are supporting an innovative Bio-MedTech company operating at the intersection of advanced therapies, biologics, wellness, and digital health and they are now hiring a VP of Regulatory Affairs. The role will be required to shape the global regulatory strategy for a fast-growing Bio-MedTech expanding across the UK, EU/Switzerland, US,...

ARTO

Nottingham

Vice President Regulatory Affairs

We are supporting an innovative Bio-MedTech company operating at the intersection of advanced therapies, biologics, wellness, and digital health and they are now hiring a VP of Regulatory Affairs. The role will be required to shape the global regulatory strategy for a fast-growing Bio-MedTech expanding across the UK, EU/Switzerland, US,...

ARTO

London

Vice President Regulatory Affairs

We are supporting an innovative Bio-MedTech company operating at the intersection of advanced therapies, biologics, wellness, and digital health and they are now hiring a VP of Regulatory Affairs. The role will be required to shape the global regulatory strategy for a fast-growing Bio-MedTech expanding across the UK, EU/Switzerland, US,...

ARTO

Newcastle upon Tyne

Vice President Regulatory Affairs

We are supporting an innovative Bio-MedTech company operating at the intersection of advanced therapies, biologics, wellness, and digital health and they are now hiring a VP of Regulatory Affairs. The role will be required to shape the global regulatory strategy for a fast-growing Bio-MedTech expanding across the UK, EU/Switzerland, US,...

ARTO

Bristol

Vice President Regulatory Affairs

We are supporting an innovative Bio-MedTech company operating at the intersection of advanced therapies, biologics, wellness, and digital health and they are now hiring a VP of Regulatory Affairs. The role will be required to shape the global regulatory strategy for a fast-growing Bio-MedTech expanding across the UK, EU/Switzerland, US,...

ARTO

Manchester