
Global Head End to End External Quality
At Genentech, we are dedicated to revolutionizing the pharmaceutical industry and improving the lives of patients worldwide. As the Global Head End to End External Quality, you will have the opportunity to lead a team in ensuring the highest standards of quality for our products. You will play a critical role in maintaining our reputation for excellence and compliance with regulatory agencies. We are seeking a highly experienced and motivated individual with a strong background in quality assurance and a passion for driving continuous improvement. If you are ready to make a meaningful impact on the healthcare industry, join us at Genentech.
- Develop and implement global quality strategies and policies to ensure compliance with regulatory agencies and industry standards.
- Lead and manage a team of quality assurance professionals to ensure the highest standards of quality for Genentech products.
- Collaborate with cross-functional teams to establish quality goals and objectives that align with the company's mission and values.
- Develop and maintain effective relationships with external partners and suppliers to ensure quality standards are met.
- Monitor and analyze quality data and trends to identify areas for improvement and initiate corrective and preventive actions.
- Oversee the investigation of product quality issues and implement appropriate corrective and preventive actions.
- Ensure all quality-related documentation and records are maintained and meet regulatory requirements.
- Keep abreast of industry trends and changes in regulations to continuously improve and update quality processes.
- Develop and conduct quality training programs for employees to promote a culture of quality and compliance.
- Represent Genentech in regulatory inspections and audits, and ensure timely and appropriate responses to findings.
- Drive a culture of continuous improvement by identifying and implementing process enhancements and efficiencies.
- Manage and monitor the quality budget and resources to ensure optimal utilization and cost-effectiveness.
- Act as a subject matter expert on quality-related issues and provide guidance and support to cross-functional teams.
- Foster a collaborative and inclusive work environment that promotes teamwork, accountability, and professional development.
- Uphold the company's values and standards of ethical conduct in all interactions and activities.
Bachelor's Or Master's Degree In A Relevant Scientific Field (E.g. Biology, Chemistry, Pharmaceutical Sciences)
Minimum Of 10 Years Of Experience In The Pharmaceutical Or Biotechnology Industry, With At Least 5 Years In A Leadership Role
Extensive Knowledge Of Global Regulatory Requirements And Industry Standards (E.g. Fda, Ema, Ich)
Proven Track Record Of Successfully Implementing And Managing Quality Systems And Processes Across Multiple Sites And Regions
Excellent Communication And Interpersonal Skills, With The Ability To Collaborate Effectively With Cross-Functional Teams And External Stakeholders At A Global Level.
Risk Management
Quality Assurance
Process Improvement
Data Analysis
Communication
Leadership
Quality Control
Audit management
Regulatory compliance
Stakeholder
Supplier Auditing
Quality Management System
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Critical thinking
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Global Head End to End External Quality in South San Francisco, CA, USA is $150,000-$250,000 per year. However, this can vary depending on factors such as experience, qualifications, and the specific company or industry the individual is working in.
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Genentech, Inc., is a biotechnology corporation which became a subsidiary of Roche in 2009. Genentech Research and Early Development operates as an independent center within Roche. As of February 2020, Genentech employed 13,638 people.

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