Manufacturing Visual Inspection (2nd shift)

Aequor; Fremont (CA); On-site; USD 33,000 - 47,000; Full time

Job summary

Aequor in Fremont, CA seeks a Manufacturing Visual Inspection technician for the 2nd shift on a 12-month contract.

You will perform routine unit operations in visual inspection in a multi-product pharmaceutical facility, follow cGMP procedures, support filling and packaging, and maintain training and batch records while ensuring safety and quality.

Requires 1+ year GMP experience, detail orientation, and ability to work with MES and SOPs.

Qualifications

• 1+ year experience in a cGMP regulated industry.
• Detail-oriented work in a complex technical setup with quality focus.
• Strong written and verbal communication skills.
• Experience with computer-based MES and SOPs.
• Ability to work in a high performing team.

Responsibilities

• Perform routine unit operations in visual inspection per SOPs.
• Operate with limited supervision and adhere to cGMP standards.
• Support drug product filling, packaging, and related activities.
• Coordinate logistics, batch records, work orders, and training documents.
• Maintain production areas and contribute to quality investigations.

Skills

cGMP experience

Detail-oriented

Strong communication

MES experience

SOP reading

Teamwork

Visual acuity

Education

High school diploma

Biotech vocational training or associate/bachelor's degree

Tools

MES systems

Job description

Manufacturing Visual Inspection (2nd shift)

Location: Fremont, CA

Duration: 12 Months contract

Pay Rate: $29/hr w2 without benefits

Schedule Notes:2nd Shift: Mon-Fri, 2PM-10:30PM

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
• -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.

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

Education:

• High school degree + minimum 1 year work experience in GMP regulated industry
• Associates/Bachelor's degree or biotechnology vocational training preferred