Job Type:	permanent	Duration:
Category:	Project or Program Mgmt.	Recruiter Reference:	mac2023
URL for Applications:		Salary:

Our client is a leading manufacturer of their product range globally and they are looking to employ an additional integral person within their planning team.
Main duties will include –
 Providing the support with generating documentation relating to the technical fil for regulatory submission of their product range
 Managing product timelines and project team workloads
 Generating project documentation in line with ISO practises.
 Working closely with the customer and design team.
 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 analyse,
 Developing product test methods , basic data analysis/evaluation to determine or prove safety and product conformance
 To function within all regulatory requirements and quality systems
Candidate Attributes –
 Ideally candidates will come from an Bio Engineering/medical based qualification
 Practical experience within medical device development fields
 Experience in project management
 Knowledge of design and development risk management processes
 Documentation writing skills

Please contact Julie at the Industrial team for further information or call (01842) 820409

Qualifications
Engineering or medical based degree
Skills

Engineering, Project engineering, ISO1384, Medical, UKCA/MDR/FDA, Communication skills