Visual Inspector, Manufacturing job in Fremont, CA
Fremont, CA CorTech LLC
| Job Ref: | 376276 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | Market/Per Hour |
| Remote: | No |
Location |
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| City: | Fremont, CA |
| Post Code: | 94555 |
| Map: |
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Description |
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Position Overview We are seeking a detail-oriented Visual Inspection Technician to support drug product manufacturing in a multi-product, GMP-regulated facility. This position performs routine and advanced visual inspection operations while supporting filling, packaging, logistics, documentation, and other manufacturing activities. The ideal candidate is comfortable working in a highly regulated environment, has strong attention to detail, and maintains a quality-first and ?right the first time? mindset. Key Responsibilities Perform routine visual inspection activities related to drug product manufacturing. Perform advanced visual inspection, palletizing, cleaning, inspection hood preparation, and other manufacturing operations following appropriate training. Support drug product filling and packaging activities. Perform logistics coordination and material movement activities. Execute batch records accurately and in accordance with cGMP requirements. Complete equipment use logs and maintain accurate manufacturing documentation. Initiate and track work orders. Support manufacturing and improvement projects. Assist with creating and maintaining training kit documentation. Operate computer-based manufacturing systems and MES/BioMES. Follow all established SOPs, manufacturing procedures, cGMP, and cGDP requirements. Identify and report abnormalities and deviations in a timely and accurate manner. Maintain production areas according to established 5S standards. Maintain required training and qualifications. Train other technicians and associates after completing the required trainer qualification. Support Quality activities, including investigations, corrective actions, and area walkthroughs. Follow all safety requirements and identify and appropriately escalate unsafe conditions or behaviors. Required Qualifications 1+ year of experience working in a cGMP-regulated industry. High school diploma with at least 1 year of GMP-regulated work experience. Strong attention to detail and ability to perform repetitive, quality-sensitive work. Ability to concentrate in a complex technical manufacturing environment. Strong written and verbal communication skills. Ability to use computer-based systems and manufacturing execution systems (MES). Ability to read and understand SOPs, work instructions, and manufacturing documentation. Ability to accurately document work in accordance with cGMP standards. Ability to work effectively as part of a high-performing team. Ability to read and see clearly for visual inspection activities. Preferred Qualifications Associate or Bachelor's degree. Biotechnology vocational training. Previous pharmaceutical or biotechnology manufacturing experience. Experience with visual inspection, drug product manufacturing, filling, packaging, or MES/BioMES systems. Physical Requirements Position may require physical exertion depending on the manufacturing activity. Lifting requirements may vary by work area, with typical lifting of up to 25 lbs. Must be able to perform visual inspection activities requiring sustained attention and clear vision. Important Pre-Employment Requirement Candidates must successfully pass vision testing, including visual acuity and color-blindness testing, before beginning the assignment. Work Environment This position operates in a highly regulated pharmaceutical manufacturing environment. Employees are expected to consistently follow established safety, quality, documentation, and GMP procedures while maintaining a strong focus on accuracy and product quality. | |
ref: (376276)
127 days ago
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