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QA/RA Technical Engineer
by Philip Cahill in Asia
Quality Assurance -Regulatory Affairs Technical Engineers- Medical Devices
Essential Skills / Experience
3/4 years experience within R&D / QA/ RA/ Compliance or Validation function
2/3 years experience in Risk, Clinical and Biocompatibility an advantage
2/3 years Medical Device Manufacturing Experience
Engineering / Science qualification
Excellent technical writing experience /skills
Fluency in English
The ability to prioritize tasks, time manage, multitask and multirole.
Key Duties:
Producing technical manuals through technical writer format
Analyzing customer complaints, identifing trends and executing corrective actions
Planning, protocol generation, testing and report generation for medical devices
Generation of technical files for medical devices
Reviewing technical files in line with EU medical devices regulatory requirements
The use of GHTF STED format and harmonised standards
Ensuring files are in compliance with the Medical Device Directive.
Supporting R&D
Behaviors and Values
Ability and Willingness to Travel to Europe and Far East
Approachable, enthusiastic, flexible and adaptable.
Ability to work on own initiative, self starter and team player
Good organisational skills and cultural awareness and sensitivity
Good judgment and problem solving ability
Send your CV in confidence to philip@jackiebrownmedical.ie
or call 01 201 6363
Jackie Brown Medical is a step ahead of other recruitment agencies in the medical industry. We recruit and offer advice in many areas allied to the Medical industry in Ireland including - Medical Sales, Logistics, Social care, Science, Pharmacy, Allied Health, Life Science, Operations, Medical Admin, Production, Medical Jobs Finance, Nursing, Radiography, Supply Chain and Doctors.
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