
MDR Compliance Project Manager
11 hours ago
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 Regulation (MDR) and related regulatory frameworks. Key responsibilities include developing project plans, setting goals, managing resources, mitigating risks, and ensuring timely delivery within scope.
Responsibilities:
- Plan, execute, and complete projects related to MDR compliance
- Develop and implement strategies to align with regulatory requirements
- Collaborate with cross-functional teams
- Ensure project milestones are met
- Manage risk assessment and mitigation strategies
- Communicate project updates to stakeholders
Requirements:
- Minimum three years of experience in project management
- Strong knowledge of MDR and regulatory compliance frameworks
- Experience in implementing regulatory policies and management systems
- Proven leadership and stakeholder engagement skills
- Excellent communication and problem-solving skills
- Fluency in both Swedish and English
Join our dynamic team and enjoy a rewarding career path with opportunities for growth and development.
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