Site Quality Leader

Role Description

The Charles City Site Quality Lead role is accountable for product quality and the site's regulatory compliance standing, ensuring adherence to all regulatory compliance requirements and cGMPs, maintaining a state of Inspection Readiness and ensuring a continuous supply of high-quality products from the site. The Site Quality Lead champions the quality culture and takes proactive steps to ensure a high level of quality and compliance at the site. The position reports to the Bio/BioPharma Platform Quality Leader. The Site Quality Lead is a member of the Site Leadership Team and participates in setting the strategic direction of the quality unit and the site as well as directing day-to-day quality operations. The position also co-chairs the site Quality Council (with the Site Lead) to drive continuous improvement and compliance objectives as well as prioritizing quality culture improvement initiatives.

Risk Assessment Process

The Site Quality Lead leads the Site Leadership through the Site Risk Assessment Process on a predetermined cadence. The Quality Lead uses data and metrics to drive continuous improvement in site quality management systems as well as Product Quality. Additionally, the role is responsible for creating and executing the Site Quality Roadmap.

Stewardship and Leadership of the Quality Culture

Establishing and Reinforcing the Quality Culture on the Site; Contributing member of the Site Leadership Team. Implementation of Quality Standards and ensure sustainability of the Quality Management Systems. Maintains Site Inspection Readiness for all applicable regulatory agencies including USDA, VMD, and European Agencies and acts as the company point of contact to lead inspection readiness for the site. Ensures that products are manufactured and released in compliance with pertinent Regulatory standards and Registration Files (and requirements of appropriate Regulatory Bodies) and partnering with the regulatory team on all activities relating to regulatory compliance. Overall Site Product Quality Stewardship owner and accountability. Stewardship and Ownership of Site Quality Management System. Promote Compliance and remediate Audit findings and ensure quality standards are maintained throughout the site.

QC Testing

Proactive Ownership of the Site Risk Assessment process including oversight of the supplier quality programs, including supplier audits and supplier qualification processes. Oversees the development and implementation of the Quality Plan / Quality Road Map. Co-Leadership of Site Quality Council and Metrics. Develop metrics to deliver product and process improvements. Ensure the Validation Master Plan is compliant and up to date. (Validation strategy and site compliance). Collect and analyze process data for new or modified products/processes. Investigates Quality related Customer Complaints. Collaborate with other organizations/sites leaders concerning quality management system activities. Staff and Leadership Responsibilities. Champion Leadership Development / Coaching of Staff; Creation of Learning Organization. Ensure Training and Development plans are in place for all Quality associates. Development of Site Quality budget and resource planning for roll-up to the Site and Company budget. Support the development of Quality goals and targets as part of the organization's strategic plan.

Organizational Relationships

This position will achieve results through Leadership of Colleagues with a direct reporting relationship as well as indirectly through partnership and collaboration with the site Lead, the extended site Leadership team, and company functions as listed below:

• Quality Platform Lead, Global Quality Organization including Quality Systems and Standards (QSS) and Global Quality Compliance Auditing.
• Bio/BioPharma Platform Leadership Team, GMS Leadership Team, Site Enabling Functions (ie: Engineering; GMT; Finance, HR etc), Operational Excellence, Regulatory Affairs, Veterinary Medicine Research and Development

Education and Experience

Biological, Chemistry or Engineering BS / MS / PhD. Demonstrated significant leadership experience in a Quality Role in Pharmaceutical / Vaccine / Animal Health / Human Health manufacturing. Operations or Quality Manufacturing preferred. USDA and European Agencies regulated work experiences desired.

Tech Skills

Excellent communicator and collaborator. Does well in a Change Management environment, Acts as a Change Agent. Problem solver, root cause analysis methodology. Process oriented mindset; data and continuous improvement orientation. Able to work well in complex environment.

Physical Position Requirements

Position located in Charles City, Iowa. Some off-site travel. Occasional non-core hour work anticipated. ACRONYM DEFINITIONSGMT: Global Manufacturing Technology QSS: Quality Systems and Standards USDA: United States Department of Agriculture VMD: Veterinary Medicines Directorate (UK Regulatory Agency)

About Zoetis

At Zoetis, our purpose is to nurture the world and humankind by advancing care for animals. As a Fortune 500 company and the world leader in animal health, we discover, develop, manufacture and commercialize vaccines, medicines, diagnostics and other technologies for companion animals and livestock. We know our people drive our success. Our award-winning culture, built around our Core Beliefs, focuses on our colleagues' careers, connection and support. We offer competitive healthcare and retirement savings benefits, along with an array of benefits, policies and programs to support employee well-being in every sense, from health and financial wellness to family and lifestyle resources.