Job Description:
- Payrate: $27.78/hr W2
- Duration: 6 months contract – with possible extension based on performance and business needs.
- 1st Shift: Mon-Fri; 6am – 2:30pm.
- High school diploma minimum.
- Experience in visual inspection in a manufacturing facility.
- Minimum 1 year work experience in GMP regulated industry/pharma industry.
- Ability to concentrate on detail-oriented work in a complex technical setup with a Quality and “Right the first-time” mindset.
- Ability to work with computer-based systems and manufacturing execution systems (MES).
- Ability to read and understand SOPs and instructions and document work in a written format applying cGMP standards.
- Must be able to read and see clearly.
- Ability to lift 25 lbs. and required to participate and have acceptable result from vision testing including color blindness.
Responsibilities:
- 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.
- Executes independently with adequate training, complex fundamental operations as visual inspection, advance visual inspection, palletizing, cleaning, inspection hood prep for operations, BioMES Operations and Exceptions.
- Performs internal support duties including assisting drug product filling and packaging.
- Executes independently with adequate training fundamental operations: Logistics Coordination, Batch record executions, Equipment use logs, Work order initiation and tracking, Support Projects.
- Support Creation/Maintain Training Kits Documents work according to cGMP and cGDP.
- Adheres to established regulations and follows cGMP established by site.
- Reports abnormalities and deviations in a timely and accurate manner.
- Adheres to safety standards, identifies unsafe situations / habits, and escalates appropriately.
- Maintains production areas according to predefined standards (5s).
- Maintains own training within compliance and trains other technicians and associates on operations upon completion of trainer qualification.
- Contributes to Quality activities such as supporting investigations, corrective actions and area walk throughs.
If you are interested in hearing more about the position, please respond to this posting with your resume attached.
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