Description
The role leads manufacturing and packaging equipment support, process engineering, continuous improvement, quality validation, and regulatory compliance in a pharmaceutical manufacturing environment. Responsibilities include troubleshooting equipment, improving OEE and throughput, leading root cause analysis and equipment qualification, supporting process validation and technology transfers, and maintaining FDA and cGMP documentation. The position requires a bachelor's degree in an engineering discipline, at least five years of experience in pharmaceutical manufacturing or another regulated industry, and knowledge of validation, Lean, Six Sigma, SAP, and cross-functional leadership.
