Regulatory Affairs Specialist

Are you an experienced regulatory affairs and quality assurance professional looking for a new challenge? If so, we have just the opportunity for you! LFH is a top medical device consultancy company that is seeking a Regulatory Affairs & Quality Assurance Consultant for fixed term contract of 12 months with possible extension to join our dynamic team. We...

Are you an experienced regulatory affairs and quality assurance professional looking for a new challenge? If so, we have just the opportunity for you! LFH is a top medical device consultancy company that is seeking a Regulatory Affairs & Quality Assurance Consultant for fixed term contract of 12 months with possible extension to join our dynamic team. We...

The Senior Regulatory Affairs Specialist is responsible for ensuring medical device regulatory compliance with national and international legislation for projects, product and new market clearance. You will manage specific regulatory objectives to meet the companys Strategic Plan and Department Operational Objectives. Assisting and sometimes deputising for...

The Senior Regulatory Affairs Specialist is responsible for ensuring medical device regulatory compliance with national and international legislation for projects, product and new market clearance. You will manage specific regulatory objectives to meet the companys Strategic Plan and Department Operational Objectives. Assisting and sometimes deputising for...

Senior Regulatory Affairs SpecialistAustin Vita is seeking a highly skilled Regulatory Affairs Expert to play a critical role in ensuring the medical device regulatory compliance of our projects, products, and new market clearances.Manage specific regulatory objectives to meet the company's Strategic Plan and Department Operational Objectives.Assist and...

Job DescriptionAustin Vita is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our Quality and Regulatory Affairs department, you will play a critical role in ensuring the company's medical devices comply with national and international legislation.Key Responsibilities:Regulatory Compliance: Manage regulatory...

Job DescriptionAustin Vita is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our Quality and Regulatory Affairs department, you will play a critical role in ensuring the company's medical devices comply with national and international legislation.Key Responsibilities:Regulatory Compliance: Manage regulatory...

**The Role** The Regulatory Affairs Specialist will report to the Commercial Director. This is expected to be a hybrid role, 3 days per week working from home and 2 days based South-West London. The person should be located a commutable distance to the office.. Working together with colleagues in Germany, the Regulatory Affairs Specialist will be required...

Job Title: Senior Regulatory AffairsJob Summary:We are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team at MSI Group Limited. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with regulatory requirements for Class I, II, and III medical devices.Key Responsibilities:Develop and...

Are you an experienced regulatory affairs and quality assurance professional looking for a new challenge? LFH is a top medical device consultancy company that is seeking a Regulatory Affairs & Quality Assurance Consultant for fixed term contract of 12 months with possible extension to join our dynamic team. We work with varying companies, that have diverse...

Are you an experienced regulatory affairs and quality assurance professional looking for a new challenge? LFH is a top medical device consultancy company that is seeking a Regulatory Affairs & Quality Assurance Consultant for fixed term contract of 12 months with possible extension to join our dynamic team. We work with varying companies, that have diverse...

The Senior Regulatory Affairs Specialist is responsible for ensuring medical device regulatory compliance with national and international legislation for projects, product and new market clearance. You will manage specific regulatory objectives to meet the company’s Strategic Plan and Department Operational Objectives. Assisting and sometimes deputising...

The Senior Regulatory Affairs Specialist is responsible for ensuring medical device regulatory compliance with national and international legislation for projects, product and new market clearance. You will manage specific regulatory objectives to meet the company’s Strategic Plan and Department Operational Objectives. Assisting and sometimes deputising...

**Regulatory Affairs Officer - West London Office** Initial 12 month FTC Our client's product portfolio demonstrates an exceptionally innovative and successful track record in the fields of Urology, Endocrine Oncology, Gastroenterology, Endocrinology (Growth) and Reproductive Health (Infertility and Obstetrics). The common thread is that the Company...

About Us: Welland Medical is the part of Clinimed Holdings Limited group, a leading name in Healthcare and Medical Equipment industry. Clinimed Holdings Limited is a group of companies founded in 1982 following the acquisition and formation of number of additional companies within the group. Welland Medical brings to market the best and most innovative...

About Us: Welland Medical is the part of Clinimed Holdings Limited group, a leading name in Healthcare and Medical Equipment industry. Clinimed Holdings Limited is a group of companies founded in 1982 following the acquisition and formation of number of additional companies within the group. Welland Medical brings to market the best and most innovative...

Post Market Regulatory Affairs ManagerSinclair is seeking a Regulatory Affairs Manager to lead our Post Market Regulatory Affairs Team. In this role, you will oversee product market approvals in line with global regulatory standards and internal policies. You will collaborate closely with our Injectables manufacturers, Business, and Commercial teams to...

As Head of Quality and Regulatory Affairs you will manage the Quality, Regulatory and Clinical Teams for an exciting Medical Device Manufacturer working on Class III Devices. Giving overall guidance and leadership to QA/RA functions including product registration, complaint handling and reporting, internal/external auditing of the quality systems and...

Welland Medical is the part of Clinimed Holdings Limited group, a leading name in Healthcare and Medical Equipment industry. Clinimed Holdings Limited is a group of companies founded in 1982 following the acquisition and formation of number of additional companies within the group. Welland Medical brings to market the best and most innovative products...

Welland Medical is the part of Clinimed Holdings Limited group, a leading name in Healthcare and Medical Equipment industry. Clinimed Holdings Limited is a group of companies founded in 1982 following the acquisition and formation of number of additional companies within the group. Welland Medical brings to market the best and most innovative products...