Project Coordinator MDR Compliance

TN Sweden is a global Contract Research Organization (CRO) partnering with biotechnology and pharmaceutical companies throughout their clinical development journey. We offer full service capabilities, resourcing and Functional Service (FSP) solutions.The Project Manager – MDR Compliance leads and coordinates efforts to ensure adherence to Medical Device...

About this roleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey.We provide full service capabilities, resourcing, and Functional Service (FSP) solutions to support clients' needs in the field of medical devices...

At TN Sweden, we are a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions.The Clinical Lead MDR is responsible for leading and coordinating...

About UsWe are TFS HealthScience, a leading global mid-size Contract Research Organization (CRO) partnering with biotechnology and pharmaceutical companies throughout their entire clinical development journey.Our team provides full service capabilities, resourcing, and Functional Service (FSP) solutions to support clients' needs in the field of medical...

About This RoleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey.Our expertise includes full service capabilities, resourcing, and Functional Service (FSP) solutions. We are dedicated to supporting our clients'...

TN Sweden is a mid-size Contract Research Organization (CRO) offering innovative solutions for biotechnology and pharmaceutical companies. Our services include full service capabilities, resourcing and Functional Service (FSP) solutions.The Regulatory Affairs Specialist – MDR Compliance plays a crucial role in ensuring adherence to Medical Device...

About TFS HealthScienceWe are a leading global mid-size Contract Research Organization (CRO) partnering with biotechnology and pharmaceutical companies throughout their entire clinical development journey.Our team provides full service capabilities, resourcing, and Functional Service (FSP) solutions to support clients' needs in the field of medical devices...

Dentatus AB is looking for an experienced Regulatory Compliance Manager to join their team. The ideal candidate will have a strong understanding of ISO 13485, ISO 14971, and MDR 2017/745 requirements. They will lead the creation and revision of MDR technical documentation, ensure products meet regulatory standards, and drive product compliance.Key...

Main ResponsibilitiesCoordinate/act as host during inspections and/or audits by notified bodies and authorities.Provide expert knowledge in Qbtech Management Systems, including ISO 13485, 21 CFR 820, ISO 27001, EU-MDR 2017/745, and other country-specific medical device legislations.Support the Product Development Team in ensuring compliance with Medical...

Dentatus AB is seeking a highly skilled Medical Device Project Manager to coordinate projects related to product support and improvements. The ideal candidate will have experience in medical device manufacturing or production, adherence to GMP and GDP standards, and a strong understanding of ISO 13485, ISO 14971, and MDR 2017/745 requirements.Key...

Senior Project Coordinator - SAPWe are seeking a highly organized and detail-oriented Senior Project Coordinator to support our SAP implementation projects.In this role, you will be responsible for providing administrative support to project managers, coordinating project logistics, and ensuring compliance with company policies and procedures.The successful...

Promote Project helps Scandinavian companies find and collaborate with the best tech talents.We focus on building long-term, full-time remote relationships that drive growth and success.Job Description:We are looking for an experienced Automotive Compliance Expert to join our team immediately. The ideal candidate will have a strong background in automotive...

Promote Project seeks an experienced Compliance Specialist for EV Systems to join our team immediately.The ideal candidate will have a strong background in automotive compliance, particularly in electric vehicle systems and charging infrastructure.Key Responsibilities:Manage and oversee compliance matters as a regulatory expert.Conduct thorough risk...

Job Title: Technical Project LeadRole Overview:This role involves driving critical package deliverables, resources, assurance requirements, and interfaces as a key member of our Unit.Main Responsibilities:Deliverable Management: Establish lists (MDR) of project phase critical technical documents and deliverables for review and assurance.Technical Oversight:...

Promote Project is seeking an experienced Electric Vehicle Regulatory Compliance Lead to join our team immediately.The ideal candidate will have a strong background in automotive compliance, particularly in electric vehicle systems and charging infrastructure.Main Responsibilities:Manage and oversee compliance matters as a regulatory expert.Conduct thorough...

About the RoleWe are seeking a highly skilled Technical Project Coordinator to join our team at Wrknest. In this role, you will be responsible for ensuring smooth project execution and aligning project goals with organizational objectives.BAM operates under Part 21, focusing on new product development within aviation. Projects can range from delivering...

About UsArka Energy AB is a leading solar system installation company committed to sustainable energy solutions. Our mission is to drive the transition to clean and sustainable energy.Job DescriptionWe are seeking a dynamic and detail-oriented Project Coordinator to join our growing team. As a Project Coordinator, you will play a pivotal role in ensuring the...

Key Responsibilities:Develop and manage Quality Management System (QMS) processes to ensure compliance with medical device regulations (MDR, ISO 13485, FDA).Support management of CAPA, non-conformance, change management, and audits.Conduct QA reviews, investigate non-conformance, and manage CAPA.Analyze quality data and identify training needs.Address...

Wequel is looking for a Project Coordinator to support our Automotive Systems Team.About the JobSupporting the team in developing and testing brake and air systems.Ensuring quality, safety, security, and legal compliance of control systems.Collaborating with other development sites within Wequel.The ideal candidate will have a strong understanding of...

The Dental Product Development Lead at Dentatus AB will play a crucial role in driving product innovation and regulatory compliance. The ideal candidate will have experience in medical device manufacturing or production, adherence to GMP and GDP standards, and a strong understanding of ISO 13485, ISO 14971, and MDR 2017/745 requirements.Key...