-6 month contract
-Pay: $28.54/hr
1st Shift: Mon-Fri, 6:00AM-2:30PM
Duties:
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 trainer qualification.
-Contributes to Quality activities such as supporting investigations, corrective actions and area walk throughs.
Skills:
-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.
PHYSICAL DEMANDS:
- Duties of this position may require the incumbent to exert some physical effort.
-Lifting requirements may vary dependent on the drug product manufacturing visual inspection area activity. Weight is typically no more than 25 pounds.
- Employees required to participate and have acceptable result from vision testing including color blindness.
Education:
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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