Job Title: Manufacturing Visual Inspection
Location: Fremont CA
Duration: 6 months
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 such as visual inspection advance visual inspection palletizing cleaning inspection hood prep for operations BioMES Operations and exceptions.
- Performs internal support duties including assisting with drug product filling and packaging.
- Executes independently with adequate training in 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 a GMP-regulated industry
Associates/bachelors degree or biotechnology vocational training preferred
Job Title: Manufacturing Visual Inspection Location: Fremont CA Duration: 6 months 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...
Job Title: Manufacturing Visual Inspection
Location: Fremont CA
Duration: 6 months
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 such as visual inspection advance visual inspection palletizing cleaning inspection hood prep for operations BioMES Operations and exceptions.
- Performs internal support duties including assisting with drug product filling and packaging.
- Executes independently with adequate training in 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 a GMP-regulated industry
Associates/bachelors degree or biotechnology vocational training preferred
View more
View less