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Duties & Responsibilities:
Other duties that may be assigned from time to time.
Minimum Qualifications:
PC literate with good skills in MS Office (Word and Excel) programs
Working knowledge of GDP (Good Documentation Practices)
Good verbal and written communication skills
Must be able to work with and without supervision.
Knowledge on Document management.
Language: Must speak and write English well.
Preferred Qualifications:
Prior experience with quality control systems
Familiar with Part 820 Quality Systems Regulation.
Familiar with ISO 13485 Standards.
Familiar with GMP (Good Manufacturing Practices);
Familiar with Agile, and Expandable ERP systems
Expertise of manages of Bill of Material.
1 year experience within the Medical Device industry.
Education:
Diploma. Professional Cert is an added advantage.
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