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
Skills Required
Engineering, Project engineering, ISO1384, Medical, UKCA/MDR/FDA, Communication skills
Qualifications Required
Engineering or medical based degree
Keywords
Engineering, Project engineering, ISO1384, Medical, UKCA/MDR/FDA, Communication skills
JBRP1_UKTJ