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Project Manager
4 months ago
**Project Manager**
**Mildenhall, Suffolk**
Within this role you will take a project leading role in bringing medical projects from concept/design stage, through regulatory approvals and into commercial products.
You will ideally have a background in medical devices, good leadership qualities and excellent communication skills. Working for a market leading company you will also be required to travel both globally and within the UK for certain projects.
**Start**:ASAP
**Location**:Mildenhall, Suffolk
**Salary**:££Competitive depending on experience
**Hours**:40 hours a week Monday
- Friday flexible working
**Duration**:Permanent
**Benefits**: 20 days holiday + 8 bank holidays, pension scheme, formal training and development, company social events. After 1 years service you will be eligible for the enhanced benefits package which includes sickness and an enhanced pension.
**Duties**:
- Working closely with the stake holders to gather relevant concept information
- Facilitate in the concept and design of products that meet the projects needs
- Provide project leadership that includes management of budget, timeline and resources
- Generation of project documentation in line with ISO 13485 and other medical device regulatory requirements
- Generation of regular project update reports
- Attend and organise regular project meetings
- To engage relevant vendors and subcontractors to support the needs of the project
- Develop product test methods, data analysis and evaluations to determine or prove product performance and reliability
- To function within all quality systems and regulations - related to medical devices
- Global and UK travel may be required to satisfy the needs of the project
- Support in the design, concept and development of product manufacturing equipment
- Attend relevant training courses
**Skills/Experience Required**:
- Lead projects to develop new products that meet the customers and companies requirements
- Implement projects according to project management principles
- Maintain compliance to regulatory and quality systems
- Good leadership qualities
- Cross functional team work skills
- Knowledge and understanding of project management
- Problem-solving skills
- Excellent verbal and written communication skills
- Previous experience within medical devices
