Genentech Work Values

Daily Duties at Genentech:

* Worked on combination product device development * Assisted in developing and reviewing design transfer documents for: --- Design FMEA --- Design Change Assessment --- Hazard Analysis --- Tolerance Analysis Report --- Product Specific Requirements * Worked on Human Factors Engineering plan * Reviewed Design Verification Test Protocols * Reviewed Traceability Matrix

What they like about Genentech:

You give high priority to hiring firms with prestige. Market reputation and prestige of a firm may be determined through on-line research, and conversations with individuals working in your target industry. Note that firms "in the public eye" receive a great deal more critical publicity and attention than those operating with more anonymity. So as you assess your employment opportunities, be sure to seek out the positive aspects of the firm's reputation in addition to noting negative publicity the company may have received.

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: