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Job description
Location: Charles City, IA
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.
The role has ownership of the Site Risk Assessment Process - leading the Site Leadership through the 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 within the Quality Function as well as across the Site
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.
Ensure 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
Ensuring QC Testing meets Regulatory Compliance and GMPs via overseeing development and implementation of standards, methods and procedures for inspecting, testing and analyzing both raw materials and finished products.
Proactive Ownership of the Site Risk Assessment process including oversight of the supplier quality programs, including supplier audits and supplier qualification processes.
Oversee 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
Provide the primary groups or key positions that this position will have interactions with as a regular part of the position responsibilities. Include any external interactions as appropriate.
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* to assure quality goals and strategic objectives are met.
*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
Fluent with Six Sigma and/or Lean Manufacturing
TECHNICAL SKILLS REQUIREMENTS
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 DEFINITIONS
GMT: Global Manufacturing Technology
QSS: Quality Systems and Standards
USDA: United States Department of Agriculture
VMD: Veterinary Medicines Directorate (UK Regulatory Agency)
Full time Regular Colleague
Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis.
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Worksite address
charles city, IA, 50616, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.