Senior Director of Site Operations (Biotech)

Kelly Science is seeking a Senior Director of Site Operations for a growing facility located in the Union City, GA area.Relocation Assistance is available for qualifying candidates***** $190,000-250,000/year depending on experienceBonus ***** $30%Employment ***** Full Time; Direct hireSome travel required to other site & conferences**As the Senior Director of Site Operations, you are responsible for leading manufacturing in commercial immunotherapy facilities.Job *Ensure business processes, procedures, and resources are in place for the safe and compliant production of biotech products.Lead or participate in cross-functional teams to develop policies, procedures, and practices for FDA licensed drug products.Represent technical operations at the Steering Committee when dealing with external clients.Manage technical operations at the companys commercial facilities and contract manufacturing sites.Lead site EHS&S teams to uphold company safety standards and corporate programs.Collaborate with cross-functional teams to ensure compliance with cGMP guidelines for clinical and commercial manufacturing.Interface with customers and the FDA during audits and inspections.Develop and achieve enterprise-wide and site performance goals.Conduct regular metric reviews across manufacturing, safety, engineering, and quality teams.Oversee department and site budget reviews, including cost of goods sold (COGS).Facilitate the planning and execution of various technical programs and projects.Coach, develop, and retain talent across all levels.Build proactive cross-functional relationships with various operations and departments.Contribute to corporate development of methods, techniques, and evaluation criteria for projects and programs.Identify problems, lead resolutions, and escalate issues as needed.****Bachelors degree in Life Science, Engineering or a related field. Advanced degree is strongly preferred. 10-15 years of experience within the pharmaceutical, biotechnology or life sciences industry with a strong background of cGMP manufacturing environment. Previous experience within urology/oncology areas is strongly preferred. Must have extensive experience commercial manufacturing experience. 7+ years of leadership experience managing cross functional teams and multi-site operations. Must have experience in other crucial areas including plant operations, EHS, warehouse, logistics, supply chain, quality assurance, and regulatory compliance.

Created: 2025-05-31