We are seeking a technical resource to support Sterile Manufacturing Operations, with a focus on inspection engineering activities and parenteral inspection technologies, supporting ongoing operations, product transfers, and continuous improvement initiatives. Key Responsibilities Lead inspection engineering activities Develop and implement new inspection technologies Provide support for product transfers Deliver operational support of inspection systems for sterile/biologic products Lead process improvements Execute validation and line trials Troubleshoot inspection equipment Manage inspection-related projects to ensure compliance, quality, and efficiency Collaboration Collaborate cross-functionally with manufacturing, engineering, quality, and validation teams Ensure alignment with site priorities and regulatory requirements Requirements Qualifications / Requirements Problem-solving capabilities Experience in pharmaceutical sterile manufacturing environments Scientist with experience...