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 of Pharmaceutical Manufacturing supervises the manufacture of Heparin Sodium Active Pharmaceutical Ingredients (API) and other pharmaceutical products at our Smithfield BioScience manufacturing site in Cincinnati, Ohio. The successful candidate will provide overall technical leadership to the manufacturing team, while promoting operational excellence, employee development and continuous process improvement. The position is responsible for ensuring both profitability and compliance with cGMP requirements. The Senior Director Pharmaceutical Manufacturing is a member of the senior management team, reporting directly to the Managing Director (site head). Responsibilities Drives the successful performance of the production manufacturing department, including direct oversight of manufacturing operations managers and plant engineers. Leverages technical skills and provides practical solutions to improve API processing efficiency while maintaining a high level of cGMP compliance. Promotes a customer-focused, right-first-time manufacturing environment. Develops and leads strategies and projects, such as capital improvement projects, to meet current and future business objectives. Ensures facilities and equipment are maintained in clean, good operating condition. Ensures clear, accurate and complete documentation of manufacturing activities. Provides leadership that promotes safety, environmental and cGMP compliance. Reviews and approves standard operating procedures, qualification and validation documentation, and technical reports. Participates in investigations and helps drive timely, effective, and compliant solutions to complex business and quality issues. Attracts, develops, and retains a highly skilled team through effective hiring, training, development, coaching and mentoring and performance management. Ensures timely completion of training for employees to meet Company and regulatory requirements. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. May perform other duties as assigned. Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals to perform the essential functions. Bachelor's degree (B.A.) from an accredited four-year college or university in Chemistry, Chemical engineering, Biochemistry or Pharmaceutical Sciences with 12+ years of relevant manufacturing experience in an API or pharmaceutical manufacturing facility; or an equivalent combination of education and experience, required. 5+ years of demonst