Overview
On Site
$21 - $27
Contract - W2
Contract - 12 month(s)
No Travel Required
Skills
PACKAGING
SOPS
CGMP
VISUAL INSPECTION
BIOTECHNOLOGY
Job Details
Job Description:
Pay Range: $21.80hr - $27.80hr
Duties:
- 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 and 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 the trainer qualification.
- Contributes to Quality activities such as supporting investigations, corrective actions, and area walk throughs.
- 1 or more years of experience in cGMP regulated industry.
- Ability to concentrate on detail-oriented 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 in a written format applying 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.
- High school degree + minimum 1 year work experience in GMP-regulated industry
- Associates/Bachelor s degree or biotechnology vocational training preferred
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