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 highly value a work environment built on a formal structure, rules, and regulations. You do not enjoy the unpredictability of shifting priorities and deadlines that upset your routine. You require and enjoy direction, input and accountability as part of your work environment. You have a strong need to participate in making key decisions and feel left out if your superiors or co-workers do not seek your input when making decisions. You thrive on providing good customer service to both internal or external customers, and doing so makes you feel good.

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: