Site Quality Lead

Zoetis • Kalamazoo, MI

75d

About The Position

The Kalamazoo 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 product 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 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 managing 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.

Requirements

• 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
• FDA, USDA, and European Agencies regulated work experiences desired.
• Fluent with Six Sigma and/or Lean Manufacturing

Nice To Haves

• 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.

Responsibilities

• Establishing and Reinforcing the Quality Culture on the Site; Contributing member of the Site Leadership Team
• Implementation of Quality Standards and ensures sustainability of the Quality Management Systems
• Maintains Site Inspection Readiness for all applicable regulatory agencies including FDA 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.
• Promote Compliance, 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 improvement.
• 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 organization/sites leaderships concerning quality management system activities.
• 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.

What This Job Offers

• Job Type: Full-time
• Industry: Chemical Manufacturing
• Education Level: Master's degree
• Number of Employees: 5,001-10,000 employees