Easter Seals Jobs

If you are currently employed at Smithfield, please log into Workday and submit your application through the Jobs Hub. A great job-and a great future-awaits you at Smithfield Foods. We're an $18 billion U.S. food company with nearly 60,000 employees worldwide. We're looking for motivated people who want to join our team and grow lasting and meaningful careers with us. Join our family today. Apply Now! Your Opportunity Our team members receive industry-competitive salaries and are eligible for great benefits packages: Competitive Pay Annual Bonus Earning Potential Comprehensive Health Insurance, Retirement Benefits and More Education benefit available to full and part time Smithfield team members on their first day of employment. Open to moving? We will help! Ask about our Relocation Assistance packages! In addition, we offer opportunities for career growth, professional development, and tuition assistance. The Senior Director, Quality has the responsibility for the strategic design, implementation, and management of the quality and regulatory systems for Smithfield BioScience including the following areas: Maintain strict compliance to pharmaceutical and medical devices standards to ensure regulatory, FDA, customer, and internal cGMP requirements by leading the Quality Control, Quality Assurance and Regulatory Affairs teams. Auditing and testing systems for in-process and finished products to ensure conformance to internal, customer, and regulatory requirements. Quality programs including supplier information, qualification, and auditing systems. Corrective and preventative action to ensure conformity with established standards. The incumbent also leads interactions with Customers, Product Development, Sales and Supply Chain leadership to develop systems and standard operating procedures to meet internal and customer quality requirements. The Senior Director, Quality works with Senior Leadership in the identification of strategic goals and plans, advises company management in FDA regulatory policy and program matters, and recommends appropriate courses of action, along with overseeing relationships with Customers to ensure accurate technical information, specifications and resolve customer complaints. Core Responsibilities Designs and manages quality management and compliance systems that ensure optimum product performance and maintains leading knowledge in the biological pharmaceutical products field. Leads investigating and implementing corrective/preventative action for customer complaints, nonconforming products, and nonconforming systems. Develops and manages procedures and work instructions to ensure conformance to specifications, quality systems, and good laboratory practices. Maintains a close relationship with Operations and leverages R&D initiatives to facilitate quality products, and design and achieve quality goals. Manages the design and implementation of quality-related training programs for Quality Control, Quality Assurance, R&D, Regulatory Affairs and Operations personnel in performing required tests, decision making skills, statistical process control, and other areas as needed. Partners with HR and Operations to design effective training curriculums to meet best practices manufacturing processes. Leads setting direction and goals for company product quality, FDA regulation, cGMP, laboratory, facility and equipment cleaning. Prepares and maintains the company Drug Master Files (DMF) filings with the FDA. Participates as part of new project design team and reviews new products, product design and product packaging, and makes recommendations for product, pharmaceutical product safety and environmental compliance. Recommends, reviews changes, and oversees implementation, and documents any approved design changes that apply to commercial p