Regulatory Documentation

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Micro Medical Devices
23945 Calabasas Road, Suite 110
Calabasas, CA
Posted: November 29 2016
Application Deadline: No Deadline
Position: Part-time, Paid

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Description

MMD is a medical device design, Manufacture and marketing company based in Calabasas (Near Los Angeles) California. We have been in business for over 14 years and our products are tailored to the Eye Care market. We are market leaders in development of battery operated, portable devices in the ophthalmic market.

Responsibilities

Help the quality control manager in performing internal audits, and preparation for annual ISO audits. Assist our team in writing of submission documents for approving new medical devices.

Requirements

We are looking for an intern with experience in the biomedical field to help us in our quality assurance group. The ideal candidate should be very organized, able to work independently and have good English reading and writing skills. Experience with regulatory submissions and approvals is an added benefit.

Skills

Required - Biomedical Engineering, Biomedical Devices
Preferred - Writing Skills, FDA GMP

How To Apply

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