Genentech, Inc Work Values

Daily Duties at Genentech, Inc:

Write and execute validation IQ/OQ/PQ protocols and write validation reports. Review and approve validation protocols and reports for validation contractors I was supervising. Review and approve change controls and SOP document change requests. Write and revise validation department SOPs. Participate in audits of CMO and supplier facilities. Present validation reports to auditors and inspectors during internal and external audits and regulatory inspections, as required.

What they like about Genentech, Inc:

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

Validation, CIP, Cleaning, Sterilization, SIP, Process Validation, Validation Manager, Validation Engineer, Lyophilization, Aseptic Processing, Biotechnology, Medical Device

Skills

P&L responsibilities, Presentation, Ecommerce Strategy and digital marketing channels optimization - SEO, SEM, email, affiliates - for high-profile accounts., Technology Solutions, Sales Support, Software Implementation, Requirements Analysis & Specification, Leadership , Validation of facilities, utilities, equipment, product and processes, Risk management

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