Description: This role is responsible for performing inspection operations within pharmaceutical manufacturing environments, ensuring that pharmaceutical products and components meet defined quality and compliance standards in accordance with current Good Manufacturing Practices (cGMP). The incumbent conducts visual and mechanical inspection of pharmaceutical products, packaging materials, and components to identify defects, non-conformances, and deviations from established specifications. This position adheres to standard operating procedures and quality standards to maintain product integrity, safety, and compliance throughout the inspection process. The role supports the overall quality assurance function by identifying and segregating non-conforming products and reporting inspection findings accurately and in a timely manner. It contributes to maintaining a clean, organized, and compliant work area in accordance with area cleaning and sanitization protocols. The position participates in training programs to develop technical competencies in inspection techniques, regulatory requirements, and quality standards applicable to pharmaceutical manufacturing. It supports continuous improvement efforts by identifying and reporting deviations and contributing to corrective and preventive action processes. Essential Functions: • Perform visual and mechanical inspection of pharmaceutical products, packaging materials, and components to identify defects and non-conformances. • Adhere to current Good Manufacturing Practices (cGMP) and standard operating procedures during all inspection activities. • Identify, segregate, and report non-conforming products and materials in accordance with established quality procedures. • Maintain accurate and complete inspection records and documentation as required by regulatory standards. • Contribute to maintaining a clean, organized, and compliant work area in accordance with area cleaning and sanitization protocols. • Operate inspection equipment and tools in accordance with established procedures and safety guidelines. • Participate in training programs to develop technical competencies in inspection techniques and quality standards. • Support continuous improvement efforts by identifying and reporting deviations and contributing to CAPA processes. • Comply with all regulatory requirements and internal policies applicable to pharmaceutical manufacturing and inspection operations. Additional Responsibilities: Education: • Bachelors Degree (BA/BS) B. Sc. - Required • Master Degree (MS/MA) M. Sc.. - Preferred Experience: • 2 years or more in 2 - 5 Years Specialized Knowledge: Licenses: