Description:
Responsibilities:
- Assist the existing Quality team with an FDA submission
- Review all relevant documents to ensure they have been collated correctly, in the right order and format etc.
- Organise and tidy the documents in preparation for the submission.
- A lot of documents will need to be cross-referenced
- Familiarity with the FDA process or the Medical Device industry is highly beneficial
- Understanding Standards System i.e. ISO134485 / ISO21CFR820
- Detail orientated and organised mindset
- High proficiency with MS Office and software systems
- The role is an immediate start
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Organization
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Cpl
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Industry
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Management
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| Occupational Category |
Document Controller |
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Job Location
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Cork,Ireland |
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Shift Type
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Morning |
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Job Type
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Full Time
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Gender
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No Preference
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Career Level
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Intermediate
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Experience
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2 Years
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Posted at
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2022-08-04 5:16 am
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Expires on
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Expired
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