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Project Director
2 months ago
High Wycombe
Paying up to £67,500
As a seasoned Project Manager, you will be responsible for leading regulatory and clinical projects of varying scope and size through the project lifecycle. Your expertise in Medical Devices will be crucial in ensuring compliance with all applicable regulatory requirements.
What's In It for You?
- Impactful Work: You'll play a critical role in bringing life-changing medical devices to market, ensuring they meet the highest regulatory standards and are backed by robust clinical evidence.
- Professional Development: You'll have access to ongoing training and development programs, including support for certifications and attendance at industry conferences, to keep you at the forefront of regulatory and clinical expertise.
- Innovative Environment: Work alongside a talented, multidisciplinary team in a company that values creativity, innovation, and continuous improvement.
- Work-Life Balance: You will likely be asked to leave at 5pm to go home and enjoy your personal time, this company fosters a fantastic culture where your wellbeing is of utmost importance.
Key Responsibilities:
- Lead regulatory and clinical projects of varying scope and size through the project lifecycle.
- Ensure project documentation is up to date and reported in a timely manner.
- Implement new Medical Device Files to ensure compliance with all applicable regulatory requirements.
- Manage CAPAs and associated documentation, including investigation and root cause activities.
Requirements:
- Hold a Prince2 or other established project management methodology qualification.
- Have a highly disciplined and detailed approach to project management and associated timelines.
- Have experience of Line Management and task delegation.
- Experience of working with Medical Devices.
Language: en-US
