Medical Affairs Professional

Vertex Ventures HC is a clinical-stage pharmaceutical company dedicated to developing innovative medicines for underserved diseases. As a Medical Affairs Strategy Director, you will play a pivotal role in shaping the company's medical strategy and ensuring the successful launch of our Bicycle molecules.The estimated salary for this position is $180,000 -...

Job Title: Regulatory Affairs and Quality Assurance ProfessionalAbout the Role:We are seeking a skilled Regulatory Affairs and Quality Assurance Professional to join our team at Newton Colmore Consulting. As a key member of our R&D team, you will play a vital role in ensuring compliance with FDA 510k, ISO 13485, and FDA 21 CFR Part 820 standards for new...

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 Overview**We are seeking a highly skilled Regulatory Affairs and Quality Assurance Assistant to join our dynamic team at Newton Colmore Consulting Ltd. Based in Cambridge, this role offers the opportunity to work with a growing medical devices company, providing quality assurance and regulatory affairs advice on the creation of new products and...

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...

Job Description: Quality Assurance and Regulatory Affairs ExpertCompany Overview:Newton Colmore Consulting is a leading consulting firm in the medical devices industry, providing expert advice on regulatory affairs and quality assurance. We are committed to delivering high-quality services that meet the needs of our clients, and we are seeking a talented...

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...

We are recruiting for a highly motivated and organized individual to fill the role of Medical Writing Professional at Costello Medical. As a key member of our medical communications team, you will be responsible for developing high-quality scientific documents, including clinical trial reports, market access materials, and regulatory submissions.The ideal...

Regulatory Compliance SpecialistA renowned healthcare technology company is seeking a highly motivated Regulatory Affairs Manager to lead their regulatory compliance efforts across international markets. This individual will play a critical role in guiding the organization's innovative medical products through the regulatory approval process, ensuring...

About the RoleWe are seeking a skilled Physiotherapist to join our team as a Functional Assessor.This is a unique opportunity for a qualified professional like you to utilize your medical expertise in a rewarding and challenging role. As a Functional Assessor, you will be responsible for assessing individuals and determining how their disabilities or...

About the JobIn a continuous effort to grow and expand our services, ProductLife Group is looking for a Regulatory Affairs Specialist to join our team in the United Kingdom.This position plays a vital role in developing our local UK Regulatory Affairs presence, overseeing new regulatory activities related to the UK for multiple clients. You will work closely...

Role Overview: Medical Device Compliance SpecialistAbout Us:Newton Colmore Consulting is a leading consulting firm in the medical devices industry, providing expert advice on regulatory affairs and quality assurance. Our mission is to deliver high-quality services that meet the needs of our clients, and we are seeking a talented individual to join our team...

About the Job">This Clinical Data Analyst position involves working on projects that require the detailed analysis and presentation of data from clinical trials. The role is instrumental to the successful uptake of novel therapies, and you will work closely with clients to deliver high-quality results.">As a key member of our team, you will have the...

About the RoleVectura Group is a global leader in developing innovative inhaled therapies and drug-device combination products. We are seeking a highly experienced Medical Device Compliance Manager to join our regulatory affairs team.Key Responsibilities:Assume the role of Regulatory Affairs Manager with specialized expertise in medical devices and...

About Us:Bicycle Therapeutics is a pioneering pharmaceutical company dedicated to developing innovative medicines for challenging diseases. Our commitment to diversity and inclusion drives us to create a workplace where everyone can thrive. As a key member of our team, you will play a crucial role in shaping our medical affairs strategy and driving our...

About VCLSWe are a leading consulting firm offering expert regulatory services to the pharmaceutical and medical device sectors. Our team is dedicated to providing high-quality support to our clients, ensuring compliance with regulatory requirements.This 30-month programme is designed for recent graduates with an interest in medicines and a desire to build a...

Newton Colmore Consulting Ltd is a leading recruitment specialist in Medical Devices, Science, and Biotech. We are looking for a talented Regulatory Affairs and Quality Assurance Assistant to join our team. This role involves supporting the Quality Assurance and Regulatory Affairs Manager in ensuring compliance with industry standards and...

ProductLife Group is seeking a Regulatory Affairs Project ManagerWe are looking for an experienced professional to lead our Regulatory Affairs outsourcing projects/programs in the UK. The ideal candidate will have a deep understanding of EU RA regulations and be able to coordinate multiple projects simultaneously.About UsAt ProductLife Group, we pride...

Job Summary:We are looking for a highly skilled Quality Assurance and Regulatory Affairs Manager Assistant to join our team at Newton Colmore Consulting in Cambridge. As a key member of our Quality Assurance and Regulatory Affairs department, you will be responsible for supporting the manager in ensuring the development of medical devices meets strict...

Job DescriptionAs a Digital Design Intern at Costello Medical, you'll work on digital projects including interactive content, marketing materials, and website design.You'll collaborate with experienced Creative team members who will provide full training on technical aspects and client communication.A high level of organisation and flexibility is essential...