Manufacturing Visual Inspection/ Quality Inspector

Position Title: Manufacturing Visual Inspection Work Location: Fremont, CA 94555 Assignment Duration: 6 months Work Schedule: 2nd Shift (Mon-Fri, 2:00PM-10:30PM) Position Summary Executes routine unit operations in Visual Inspection as assigned related to the manufacturing of drug product in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures. Key Responsibilities Conduct visual inspection, advanced visual inspection, palletizing, cleaning, inspection hood prep for operations, BioMES operations and exceptions. Assist drug product filling and packaging. Logistics coordination, batch record executions, equipment use logs, work order initiation and tracking, support projects, maintain training kits documents. Document work according to cGMP and cGDP, adhere to regulations. Report abnormalities and deviations promptly and accurately. Adhere to safety standards, identify unsafe situations/habits, and escalates appropriately. Maintain production areas according to predefined 5S standards. Maintain training compliance and train other technicians upon completion of trainer qualification. Contribute to quality activities such as investigations, corrective actions, and area walk‑throughs. Qualifications & Experience At least 1 year of experience in a cGMP regulated industry. Detail‑oriented, ability to work in a complex technical setup with a quality and "right the first time" mindset. Strong written and verbal communication skills. Ability to work with computer‑based systems and manufacturing execution systems (MES). Ability to read and understand SOPs and instructions and document work per cGMP standards. Ability to work as part of a high‑performing team and collaborate effectively with staff. Must be able to read and see clearly. Physical Requirements May require lifting up to 25 pounds. Physical effort required. Employees required to participate in vision testing including color blindness. Education High school diploma required. Minimum 1 year of work experience in GMP regulated industry. Associate’s/Bachelor’s degree or biotechnological vocational training preferred. Compensation Starting pay: $25.00 per hour. Equal Opportunity Employer SPECTRAFORCE is an equal opportunity employer and does not discriminate against any employee or applicant for employment because of race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability or veteran status, or any other category protected by applicable federal, state, or local laws. Please contact Human Resources at View email address on click.appcast.io if you require reasonable accommodation. #J-18808-Ljbffr Spectraforce Technologies Inc