Senior Automation Systems Administrator, Manufacturing & Lab Support

Role: Senior Automation Systems Administrator supporting biopharmaceutical manufacturing and laboratory operations. Primary objectives include configuring, maintaining, and validating automated system software to ensure cGMP compliance, supporting continuous improvement initiatives, and providing technical troubleshooting. Responsibilities encompass managing process control and monitoring systems, executing validation and qualification efforts, authoring change controls and risk assessments, leading system validation projects, and supporting system integration with platforms like LIMS. Qualifications: BS/BA in Science, Engineering, or related field with 5+ years of relevant experience; expertise in configuring and troubleshooting process automation systems per GAMP 5 guidelines; strong knowledge of cGMP biotech/pharma operations, regulatory standards, and validation practices. High-Value: role centered on cGMP process control systems, validation, and regulatory compliance within biopharma manufacturing; experience with biotech or biopharmaceutical facilities preferred. Work setup: onsite in Menands, NY, Monday to Friday; physical requirements include gowning and working in a cleanroom environment.