Technical Supervisor PC

Role: Manufacturing Supervisor responsible for overseeing production processes, ensuring quality, safety, and efficiency in pharmaceutical manufacturing, particularly in transdermal products. Key objectives include maintaining compliance with cGMP, optimizing operations, and managing resources. Responsibilities encompass staffing alignment, troubleshooting, quality record completion, cross-department coordination, safety enforcement, process improvements, and training. The role involves investigating non-conformances, implementing corrective actions, and participating in new product development and process validation teams. Qualifications: Bachelor's degree or equivalent with at least 2 years of pharmaceutical manufacturing experience or 6 years of related work. Must be familiar with cGMP, SOPs, FDA guidelines, and manufacturing principles; knowledge of transdermal technology preferred. Six-Sigma Green Belt certification is a plus. Requires strong leadership, problem-solving skills, and computer literacy. HighValue: pharmaceutical manufacturing, cGMP compliance, transdermal dosage forms, team leadership, process troubleshooting, regulatory adherence. Work setup: production/plant floor, with physical demands including lifting up to 50 pounds and working in controlled environments.