Manufacturing Visual Inspection

eTeam; Fremont (CA); On-site; USD 28,000 - 39,000; Full time

Job summary

eTeam in Fremont, CA seeks a Manufacturing Visual Inspection specialist for a 12-month assignment. The role operates on the 1st shift (Mon-Fri, 6AM-2:30PM) supporting visual inspection of drug products in a multi-product facility.

Responsibilities include executing routine unit operations, complying with cGMP and cGDP, performing batch records, and assisting with packaging. Strong attention to detail and teamwork are essential.

Qualifications

• 1 year or more of experience in a cGMP regulated environment.
• Ability to perform detail-oriented tasks in a technical setting.
• Strong written and verbal communication skills.
• Proficiency with computer-based systems and MES.
• Ability to read SOPs and document work clearly per cGMP.
• Team-oriented with reliable attendance and accuracy.

Responsibilities

• Execute routine unit operations in Visual Inspection for drug product manufacturing.
• Adhere to SOPs, cGMP rules, and safety guidelines.
• Support drug filling, packaging, and related duties as needed.
• Log batch records, equipment use, and work orders accurately.
• Assist with training, investigations, and deviations reporting.
• Maintain 5S standards and participate in area walks.

Skills

Detail orientation

cGMP experience

Written communication

Verbal communication

MES familiarity

SOP comprehension

Team collaboration

Reading clarity

Education

High school diploma

Associates/Bachelor's or biotech training preferred

Tools

MES

SOPs

Job description

Job Title: Manufacturing Visual Inspection

Location: Fremont, CA

Duration: 12 Months

1st Shift: Mon-Fri, 6AM-2:30PM

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
• 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.

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