Manufacturing Supervisor I (Sunday to Wednesday, 4:00pm - 2:30am)

Role: Manufacturing Supervisor I responsible for leading aseptic production operations, ensuring safety, quality, and regulatory compliance. Objectives include maintaining high safety standards, efficient shift coordination, and continuous process improvements. Responsibilities encompass fostering a safety culture, deploying and developing team members, managing production schedules, ensuring compliance with cGMPs and regulatory requirements, and participating in process optimization initiatives. Qualifications: Bachelor’s degree (sciences or engineering preferred), minimum two years manufacturing experience, with supervisory experience advantageous. Proficient in Microsoft Office, SAP, and familiar with safety, quality systems, and cGMPs. Experience in aseptic environments is desirable. High-Value specifics: Focus on aseptic pharmaceutical manufacturing, cGMP compliance, and process efficiency. Collaboration involves direct team leadership, with a focus on operational excellence in a regulated biopharma environment. Work setup: Not specified, but likely on-site given operational responsibilities.