We are seeking a Senior Parenteral Inspection Technology Specialist to provide technical support to a Sterile Manufacturing Operations Site, with focus on parenteral inspection technologies, sterile/biologics manufacturing, process science, validation, troubleshooting, and continuous improvement.
This role will support ongoing operations, product and technology transfers, inspection system optimization, and implementation of new inspection technologies. The resource will lead and support inspection engineering activities, including line trials, validation execution, recipe development/optimization, equipment troubleshooting, process improvements, and inspection-related projects to ensure compliance, quality, and operational efficiency.
The resource will collaborate with Manufacturing, Engineering, Quality, Validation, MS&T, Automation, and Maintenance teams to resolve technical issues, support deviations/CAPAs/change controls, and ensure alignment with GMP, site procedures, and regulatory requirements.
Education and Experience
Bachelor’s degree in Engineering, Pharmaceutical Sciences, Life Sciences, Chemistry, Biology, Microbiology, or related technical field required. Master’s degree or certifications in GMP, validation, Lean/Six Sigma, or project management are preferred.
Typically requires 8+ years of experience in pharmaceutical, biotechnology, sterile manufacturing, or parenteral operations, with strong experience in visual inspection, automated or semi-automated inspection systems, inspection engineering, equipment troubleshooting, line trials, qualification, validation, and process optimization. Experience with sterile injectables, biologics, product transfers, new product introductions, GMP documentation, deviations, CAPA, change control, and regulatory compliance is strongly preferred.
**Weil Group is proud to be an Equal Employment Opportunity Employer.**