Manufacturing Visual Inspection (2nd shift)

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

Job summary

Aequor is seeking a Manufacturing Visual Inspection technician for the 2nd shift in Fremont, CA. This role involves routine visual inspection of drug products in a multi-product facility, operating under cGMP guidelines and SOPs.

The position is a 12-month contract and requires careful documentation and collaboration with the manufacturing team. The candidate will work Mon-Fri, 2PM-10:30PM, performing duties with supervision, and will assist with packaging and related quality activities as

Qualifications

• 1+ year experience in a cGMP regulated environment.
• Strong detail orientation and accuracy in a technical setting.
• Good written and verbal communication.

Responsibilities

• Perform routine visual inspection on drug products in a multi-product facility.
• Follow SOPs and cGMP procedures in daily tasks.
• Support drug product filling and packaging activities as needed.
• Record batch activities and log deviations as required.

Skills

Detail-oriented

Quality mindset

Strong communication

Team collaboration

Reading SOPs

Education

High school diploma

Associates degree

Bachelor's degree in biotech

Tools

MES

Quality 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