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Principal Project Engineer

Mildenhall, Suffolk

Monday Friday, 40 hours per week, office based but offering flexible start and finish times.

££Competitive Salary

Benefits:

* 20 days holiday + 8 bank holidays.

* Training provided

* New, modern purpose built building.

* Friendly team.

We are working on behalf of a client who is seeking enthusiastic candidates to join their rapidly growing team. We are seeking candidates who are excited by medical device development who enjoy a varied and busy role.

As a principal project engineer you will take an integral role leading the wider project team in the development activities and generation of the required technical documentation to bring new medical devices from concept into commercial products.

Who are we?

We are Busy Bee Recruitment, an awarding-winning recruitment agency supplying both temporary and permanent staffing solutions throughout the UK to our wonderful client base.

What our client can offer you:

* To provide support with generating documentation relating to the technical file for regulatory submission of the medical products.

* Managing project timelines and project team workloads.

* Generating project documentation in line with ISO 13485 and other medical device regulatory requirements.

* Working closely with the customer to gather relevant information.

* Work closely with the design team to create a device that meets the customers needs.

* Attend and organise regular internal and customer meetings.

* Engaging with relevant vendors and subcontractors to support the needs of the project.

* Risk management and hazard analysis activities.

* Developing product test methods, basis data analysis/evaluation to determine or prove product conformance and safety.

* To function within all regulatory requirements and quality systems, particularly related to medical devices.

* Occasional UK travel may be required to satisfy the needs of the project.

What we are looking for:

* A Bio Engineering/Medical based Degree or equivalent qualification.

* Practical experience within medical device development field.

* Experience in project management (ideally of medical device projects).

* Knowledge of medical device regulations (UKCA, MDR, FDA etc.)

* knowledge of design and development risk management processes.

* Documentation writing skills and ability to use MS Office programs.

So, are you ready for your next job? Hit on the apply button today

If you have not received a response within 3-5 working days, unfortunately your application has been unsuccessful. Busy Bee Recruitment Ltd is acting as an Employment Agency for this Permanent vacancy