Genentech Work Values

Daily Duties at Genentech:

* Working on combination product device development * Drafting and developing documents for regulatory submissions * Working on Human Factors Engineering Report including: --- Task Analysis --- Use related Hazard Analysis --- Assessment of Similar devices * Performing device failure investigations * Participating in Root Cause Analysis * Conducting X-ray study for failure analysis * Updating Risk Management documents like: --- Use FMEA --- Hazard Analysis --- Design FMEA * Assisting in developing and reviewing documents for: --- Design Verification Testing activities --- Test Method Transfer Plan & Protocols --- Product Characterization Summary Report

What they like about Genentech:

The social vibrance of a hiring firm is very important to you. Your ability to make and maintain friendships there is a critical part of your decision. You would likely be dissatisfied with a workplace that is quiet, cold, or otherwise not particularly social. When you investigate a new hiring company, ask recruiters, managers, and potential co-workers about the social life and opportunities there. This is especially important when you are relocating; moving dramatically alters your social sphere both inside and outside the workplace.

Tags

Quality , Bay Area, Regulations, Medical Device, FMEA, Risk Manangement, Human Factors, Root Cause Analysis, ASQ Certified, Data Analysis, ISO 13485, FDA, QSR, GDP, Combination Product, ASQ, RAPS

Skills

Quality Assurance, FDA Regulations, ISO 13485, Risk Management, FMEA, Medical Devices, Design of Experiments, Minitab, Microsoft Office, Human Factors Engineering, Root Cause Analysis, 510k, GDP, Trend Analysis, Document Review

These are some of the questions we asked our climbers about their experiences with Genentech: