2 - 4 years
2 - 5 Lacs
Posted:20 hours ago|
Platform:
Work from Office
Full Time
To Prepare Technical Master file.
• Preparation of Component inspection standard
• Facilitated internal and external audits as per ISO 13485, ensuring robust quality systems
• Compilation of Design & Development file. • Working on New Product Development (NPD).
• Conduct Packaging Validation According to ISO 11607.
• Assisting with the preparation and review SOP.
• Working on Engineering change notice (ECN).
• Communication with other department i.e. R&D, Design & Development, Quality Control, Quality Assurance, QMS, Moulding & Extrusion.
Proven experience into Mediacl device standards working on RCA and CAPA for NC and closures
Knowledge of Electronic devices
Syrma Johari Medtech
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