2nd Shift Manufacturing Visual Inspection

Sigma Systems, Inc.; Fremont (CA); On-site; USD 42,000 - 54,000; Full time

Job summary

Sigma Systems, Inc. in Fremont, CA seeks a 2nd shift Manufacturing Visual Inspector for a 1-year contract. Onsite role with 2nd shift: Mon-Fri, 2 PM–10:30 PM.

You will execute routine operations in visual inspection for drug product in a multi-product facility, following cGMP and SOPs, and maintain training and records with accuracy. The position requires a high school diploma and at least 1 year of GMP-regulated experience, strong attention to detail, and good communication skills to work in a

Qualifications

• High school degree + minimum 1 year work experience in GMP 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 MES.
• Ability to read SOPs 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.

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 Exeptions. Performs internal support duties including assisting drug product filling and packaging.
• 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

Detail-oriented

Strong written and verbal comm.

Team collaboration

MES familiarity

Education

High school diploma or equivalent

Tools

MES

Job description

37737436 2nd Shift Manufacturing Visual Inspection, Fremont, CA, 1 year Contract
Sigma Inc is currently looking for a Manufacturing Visual Inspection to work onsite in Fremont, CA
Schedule : 2nd Shift: Mon-Fri, 2PM-10:30PM
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 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.

Requirements:

• High school degree + minimum 1 year work experience in GMP 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.

NOTE: Worker required to clear VISION TESTING (acuity & color blindness) before starting assignment.