Project Manager

at  Intersurgical

Job Advert
An exciting opportunity has arisen for an experienced Project Manager to join our thriving UK medical device manufacturing company to work within our Design and Development department.
We are looking to recruit a Project Manager who will be responsible for managing the development projects for Research and Development and Product Development.
The successful candidate will oversee, manage and priorities project tasks, manage timelines within agreed project plans and communicate status to all stakeholders whilst ensuring projects are implemented in accordance with appropriate regulatory and marketing requirements.

Key responsibilities will consist of:

• Full project life cycle ownership: successful project delivery for new and improved products in accordance with the specified technical, quality, budget, and schedule requirements
• To generate project plans and to actively track and maintain them to ensure the timely delivery of projects and alignment with business goals
• To ensure that the project information is well maintained; for example, budget costs, folders, linked projects
• To ensure compliance to FDA/NPMA/ISO 13485, as well as supporting Medical Device Directive/Regulations documentation

DESIRABLE EXPERIENCE/QUALIFICATIONS:

• Degree within project management or a related field or equivalent level qualification
• Minimum 5 years’ experience working within medical device or other relevant industry

KEY SKILLS:

• Excellent verbal and written communication skills
• Able to build good working relationships
• Able to negotiate
• Able to work well under pressure and meet deadlines
• Able to multitask and prioritise workload
• Able to make decisions
• Able to work independently as well as within a team
• Able to work effectively across a number of interrelated departments
• Self-motivated
• Keen and willing to learn
• Have a can-do attitude with an enthusiastic approach to work
• I.T. Literate – Microsoft Office
• Methodical, organised and structured approach to work
• Excellent attention to detail
• Able to gather, evaluate, critically interpret and communicate information
• Strong analytical and problem solving skills
• Able to work in a safe manner complying with Health and Safety Legislation
• Able to function in a highly regulatory environment with a focus on compliance
• Able to act in a fair and reasonable way
• High level of commitment
• Flexibility to work additional hours if required to support the business needs
• Good levels of English speaking
• Physically fit and able to perform tasks of a manual nature

• Full project life cycle ownership: successful project delivery for new and improved products in accordance with the specified technical, quality, budget, and schedule requirements
• To generate project plans and to actively track and maintain them to ensure the timely delivery of projects and alignment with business goals
• To ensure that the project information is well maintained; for example, budget costs, folders, linked projects
• To ensure compliance to FDA/NPMA/ISO 13485, as well as supporting Medical Device Directive/Regulations documentatio