Manufacturing Visual InspectionContract
California, Fremont - 94555Job Simplification
The announced job offer is made public by the firm: CorTech LLC and it was included in jobs list the date of: 2022-10-22 in the website greenenergyjobsonline.com.
It is announced that they have a job offer at the category of Trades & Services and the jobs location is in the state of California at the city Fremont, in the country US - at this current ZipCode: 94555
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Job Overview
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 Exeptions. 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 approriately.
-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 year 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 work intructions 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. Employees requires to participate and have acceptable result from vision testing including color blindness.
- Duties of this position may require the incumbent to exert some physical effort. Lifting requirements may vary dependent of the drug product manufacturing visual inspection area activity. Weight is typically no more than 25 pounds.
Education:
High school degree + minimum 1 year work experience in GMP regulated industry;
Associates/bachelors degree or biotechnology vocational training preferred.
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 Exeptions. 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 approriately.
-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 year 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 work intructions 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. Employees requires to participate and have acceptable result from vision testing including color blindness.
- Duties of this position may require the incumbent to exert some physical effort. Lifting requirements may vary dependent of the drug product manufacturing visual inspection area activity. Weight is typically no more than 25 pounds.
Education:
High school degree + minimum 1 year work experience in GMP regulated industry;
Associates/bachelors degree or biotechnology vocational training preferred.
Employer Overview
CorTech LLC
California, Fremont - 94555- Agency