Manual Visual Inspection job in Fremont, CA
Fremont, CA CorTech LLC
| Job Ref: | 376764 |
| 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 Manufacturing Technician to support pharmaceutical drug product manufacturing in a multi-product facility. This position will primarily support visual inspection and manufacturing operations while following strict GMP/cGMP procedures and quality standards. The ideal candidate will have experience working in a regulated manufacturing environment and be comfortable following detailed procedures, completing documentation, using computer-based manufacturing systems, and maintaining a strong focus on quality. Responsibilities Perform routine manufacturing operations related to visual inspection of drug products. Perform visual inspection, advanced visual inspection, palletizing, cleaning, and inspection hood preparation. Use manufacturing execution systems (MES), including BioMES, to document and manage manufacturing activities. Support drug product filling and packaging operations as needed. Complete batch records, equipment use logs, and other required manufacturing documentation. Coordinate logistics and support work order initiation and tracking. Report abnormalities and deviations accurately and in a timely manner. Support quality activities, including investigations, corrective actions, and area walkthroughs. Maintain production areas according to established 5S standards. Follow all established safety procedures and report unsafe conditions. Maintain required training and assist with training other technicians after becoming qualified as a trainer. Assist with process improvement and other manufacturing support projects. Create and maintain training materials and documentation. Perform all work in accordance with cGMP/cGDP requirements and site procedures. Qualifications 1+ year of experience working in a GMP/cGMP-regulated industry. High School Diploma required. Associate's or Bachelor's degree, or biotechnology/vocational training, preferred. Strong attention to detail and commitment to right-first-time quality. Ability to read, understand, and follow SOPs and detailed work instructions. Experience documenting work in a regulated manufacturing environment. Comfortable working with computer-based systems and MES/manufacturing systems. Strong written and verbal communication skills. Ability to work effectively as part of a team. Ability to identify and appropriately escalate abnormalities, deviations, and safety concerns. Must be able to read and see clearly. Physical Requirements Position may require some physical effort depending on manufacturing activities. Lifting requirements may vary but are typically up to 25 pounds. Important Pre-Employment Requirement Candidates must successfully pass a vision test prior to starting the assignment. The vision test includes visual acuity and color-blindness testing. | |
ref: (376764)
16 hours ago
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