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Job description
The Process Expert for Visual Inspection is responsible for developing, implementing, and continuously improving visual inspection processes for parenteral drug products in compliance with USP <790> and USP <1790> requirements. This role ensures that manual and/or automated inspection processes consistently detect particulate matter and cosmetic defects, while maintaining compliance with GMP, regulatory, safety, and environmental requirements.
Own and maintain visual inspection program documentation, ensure compliance with USP <790> and USP <1790> requirements, develop, qualify, and optimize visual inspection processes, and lead inspection lifecycle activities including method development, qualification, training, and continuous monitoring.
This role requires a strong knowledge of USP <790> and USP <1790> requirements, understanding of visual inspection principles, and experience with manual and automated inspection systems. The ideal candidate will have a Bachelor’s degree in Biological Sciences, Engineering, or related discipline, and minimum 3 years of experience in GMP pharmaceutical manufacturing, QA/QC, or visual inspection.
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Company
Construction • Design
Siegfried is a leading multidisciplinary design and engineering firm serving Northern and Central California for more than 70 years. Based in Stockton with offices in Modesto, Sacramento, San Jose, and Truckee, the company delivers integrated civil, structural, geotechnical, and landscape architecture solutions, complemented by surveying, project management, sustainable design, and grant writing services. Leveraging deep technical expertise and a collaborative approach, Siegfried helps clients navigate complex projects, supports community growth and resilience, and provides hands‑on management, regulatory guidance, and innovative design backed by advanced technology.