Inspection Jobs in Fontana, CA
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Inspection • fontana ca
Last updated: 1 day ago
Visual Inspection Technician ($20-$22 / hr DOE).This on-site position supports bulk formulation and filling operations for the sterile production of liquid injectable pharmaceutical products, ensurin...Show moreLast updated: 30+ days ago
Baseline, San Bernardino, California 92410 United States of America.Ready to rev up your career? Are you perceptive, knowledgeable about cars and interested in working as part of a team? If so, con...Show moreLast updated: 1 day ago
Visual Inspection Technician
Marquee StaffingCA, USFull-time
Quick Apply
Pre-Inspection Specialist
U-HaulSan Bernardino, CaliforniaFull-time
The average salary range is between $ 39,390 and $ 118,789 year , with the average salary hovering around $ 99,394 year .
- Alexandria, VA (from $ 65,000 to $ 234,900 year)
- Arlington, TX (from $ 39,000 to $ 195,750 year)
- Cambridge, MA (from $ 29,250 to $ 190,161 year)
- Costa Mesa, CA (from $ 41,650 to $ 179,000 year)
- Boston, MA (from $ 42,900 to $ 174,250 year)
- Charlotte, NC (from $ 31,200 to $ 157,400 year)
- San Francisco, CA (from $ 42,900 to $ 155,450 year)
- San Mateo, CA (from $ 40,202 to $ 153,982 year)
- San Jose, CA (from $ 40,560 to $ 153,982 year)
- San Bernardino, CA (from $ 39,975 to $ 151,633 year)
The average salary range is between $ 29,250 and $ 72,774 year , with the average salary hovering around $ 36,068 year .
Visual Inspection Technician
Marquee StaffingCA, US30+ days ago
Job type
- Full-time
- Quick Apply
Job description
Visual Inspection Technician ($20-$22 / hr DOE)
Position Overview
This on-site position supports bulk formulation and filling operations for the sterile production of liquid injectable pharmaceutical products, ensuring compliance with current Good Manufacturing Practices (cGMP) within a Drug Product Manufacturing environment.
Work Schedule : Monday–Friday, 8 hours / day (excluding lunch).
Start Time : Flexible between 7 : 00 AM – 9 : 00 AM (consistent daily schedule required).
Additional Hours : Overtime, weekends, and holidays may be required.
Key Responsibilities
Perform routine manufacturing tasks following internal SOPs and cGMP guidelines.
Prepare material components for manufacturing operations.
Accurately document activities in production batch records, logbooks, and other controlled forms.
Participate in inspection readiness and compliance initiatives.
Perform basic arithmetic and algebraic calculations.
Maintain cleanliness of manufacturing areas and equipment.
Assist in bulk drug formulation using lab equipment (e.g., mixers, balances, pH meters), under Class C (ISO 7) conditions.
Support sterile filtration activities under Class C (ISO 7) conditions.
Assist with sterile filling of various solutions (drug product, media, buffers) using automated systems, under Class C (ISO 7) conditions.
Collect and dispose of lab waste per standard procedures.
Contribute to continuous improvement initiatives within the department.
Qualifications
Education :
High school diploma or equivalent required.
Bachelor’s degree in Engineering or Life Sciences preferred.
Experience :
1–2 years of relevant industry experience required.
Experience in a growth-oriented, cGMP contract manufacturing environment is a plus.
Skills and Competencies :
Strong time and project management skills; ability to multitask.
Effective communicator across departments and teams.
High integrity, strong work ethic, and ability to work independently with minimal supervision.