Job Description The Program Manager will serve as the right hand to the Associate Director, supporting the coordination and execution of pharmaceutical manufacturing projects. This role requires a strategic thinker with hands-on experience in both sterile and non-sterile environments, particularly in liquid dosage production. Key responsibilities include: Leading cross-functional project teams to ensure timely delivery of initiatives with minimal impact to production. Supporting shutdown planning and execution, working closely with leadership to optimize resource allocation. Collaborating with Production Operations, Engineering, Quality Assurance, and SHE teams to ensure technical and regulatory compliance. Driving continuous improvement initiatives focused on Safety, Quality, and Productivity. Managing installation and commissioning of equipment, including IQ/OQ documentation. Coordinating internal and external resources, including vendors and contractors. Ensuring all work aligns with cGMP standards and internal SOPs. Occasionally working extended hours, including weekends, to support critical project timelines. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/. Skills and Requirements Minimum 5 years of experience in pharmaceutical manufacturing Strong background in sterile and non-sterile environments, with emphasis on solid dosage forms. Proven experience managing and executing large-scale pharmaceutical projects. Ability to work closely with Production Technicians and Technical Teams to analyze and improve production processes. Familiarity with cGMP, SOPs, and Safety Standards in a 24/7 manufacturing facility. Willingness to work long weekends and overtime as needed. Strong coordination skills with cross-functional teams including Engineering, Quality Assurance, SHE, and Production Operations. Experience with solid dose manufacturing. Prior involvement in shutdown planning and execution. Ability to generate and maintain Standard Operating Procedures (SOPs). Exposure to Change Control processes and equipment qualification (IQ/OQ). Strong problem-solving skills with a proactive approach to identifying and resolving production issues.