Regulatory Affairs Manager

Job DescriptionWe are seeking a skilled Regulatory Affairs Specialist to join our team at Intuitive Surgical. As part of a 9-month project and the launch of a product in the biotechnology market, we require a candidate available immediately (within 1 month maximum). There are possibilities to continue on a permanent contract.Your Key Responsibilities:Prepare...

About the PositionWe are seeking a highly skilled Regulatory Affairs Professional to join our team at ONWARD (GTX Medical). In this role, you will play a critical part in ensuring the production and delivery of innovative therapies for individuals with spinal cord injuries.As a Regulatory Affairs Professional, your primary focus will be on upholding the...

At Voisinconsulting, we are expanding our Clinical Trial Submissions (CTS) group and 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, progressive...

Regulatory Affairs Specialist Job Description:We are seeking a skilled Regulatory Affairs Specialist to join our legal department. In this role, you will be responsible for reviewing and negotiating contracts related to clinical trials, as well as supporting other legal department projects.Responsibilities:Review and analyze various contracts, including...

As a Regulatory Affairs Engineer at Michael Page International (Switzerland) SA, you will be responsible for ensuring compliance with regulatory standards and developing process improvements.Key AccountabilitiesEnsure compliance with regulatory requirements.Develop and implement process improvements.Collaborate with cross-functional teams to achieve project...

About Our OrganizationOur organization operates in the Life Sciences sector, renowned for innovative work and a deep commitment to improving quality of life worldwide.Job OverviewEnsure compliance with relevant regulatory standards.Identify and implement process improvements.Collaborate with cross-functional teams to deliver projects on time.Provide...

As a Senior Regulatory Affairs Specialist, you will play a critical role in supporting the growth and success of our business. You will be responsible for managing regulatory submissions, collaborating with cross-functional teams, and ensuring compliance with EU regulations. In this role, you will have the opportunity to develop and implement regulatory...

Our team is seeking a highly experienced Senior Regulatory Affairs Specialist to lead regulatory efforts in New Product Development (NPD) projects and sustaining operations across designated Business Units. The successful candidate will have a deep understanding of Global medical device regulations, including ISO 13485, European Medical Device Directive...

Vision-consulting is seeking a seasoned Regulatory Affairs professional to join our Clinical Trial Submissions (CTS) group. The successful candidate will have 4+ years of experience in regulatory affairs and a strong background in Clinical Trial Submissions.This is a unique opportunity to work with a visionary leader who fosters collaboration, open...

We are seeking a highly motivated and experienced Senior Regulatory Affairs Specialist to join our team in Switzerland. As a key member of our Regulatory Affairs Department, you will be responsible for providing advanced regulatory support for NPD projects and sustaining operations across designated Business Units. This role requires a deep understanding of...

We are seeking a skilled Regulatory Affairs Engineer to join our team at Michael Page International (Switzerland) SA.Job DescriptionEnsure compliance with regulatory requirements.Implement process improvements and optimize workflows.Collaborate with cross-functional teams to achieve project goals.Provide technical guidance to team members.Prepare and submit...

Job SummaryThe HCP Compliance Manager will serve as a Subject Matter Expert on all HCP compliance matters, working closely with Legal, Sales, Training, and Marketing team members to develop and implement policies, procedures, and best practices across Europe Direct regions & Distribution Markets.This role involves developing and maintaining compliance...

We are recruiting a Regulatory Affairs professional with 4+ years of experience in regulatory affairs and a strong background in Clinical Trial Submissions to join our Clinical Trial Submissions (CTS) group at Vision-consulting.This role is ideal for someone who is passionate about People, Innovation, Passion, and Excellence (PIPE) and wants to grow...

About the RoleThis is an exciting opportunity to join our team as a Regulatory Affairs Specialist. You will play a key role in ensuring the success of our product launch in the biotechnology market. The position requires a high level of expertise in regulatory affairs and excellent communication skills.Your Key Responsibilities:Prepare and compile regulatory...

Role and ResponsibilitiesThe role involves working closely with cross-functional teams to ensure that regulatory requirements are met for the launch of a product in the biotechnology market. The position is available immediately (within 1 month maximum) and there are possibilities to continue on a permanent contract.Key Responsibilities:Prepare and compile...

Clinical Development PositionJob Summary:We are seeking an experienced Senior Clinical Development Manager to join our team. The successful candidate will have a strong background in global clinical trial management, with a focus on oncology.About the Job:The Senior Clinical Development Manager will be responsible for leading cross-functional teams in the...

We are looking for a seasoned Senior Regulatory Affairs Specialist to join our team in Aubonne. As a key member of our Regulatory Affairs Department, you will be responsible for providing advanced regulatory support for NPD projects and sustaining operations across designated Business Units. This role requires a deep understanding of EU and global medical...

Company OverviewWe are a global leader in biotechnology based between Geneva and Lausanne. We aim to revolutionize healthcare through innovative technologies.Job SummaryWe are looking for a highly skilled Regulatory Affairs Specialist to join our team. As part of a 9-month project and the launch of a product in the biotechnology market, we require a...

We are looking for a highly skilled Regulatory Affairs professional to join our Clinical Trial Submissions (CTS) group at Voisinconsulting. The ideal candidate will have 4+ years of experience in regulatory affairs and a strong background in Clinical Trial Submissions.This role offers the opportunity to work with a progressive leader who values authenticity,...

The selected candidate will lead computerized system validation (CSV) for process equipment, facilities, and MES, ensuring compliance and driving process improvements. This is a rolling 12-month contract/freelance opportunity to support a global pharmaceutical client. You will develop and execute CSV documentation for new systems and upgrades, manage...