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A leading company seeks a Visual Inspection Technician for their North Charleston location. The role demands keen attention to detail for quality assurance of sterile injectable products, ensuring compliance with GMP standards. Full benefits and competitive pay are offered, making this an excellent opportunity for those with relevant experience.
Visual Inspection Technician - 1st Shift
Job
Overview
Location :
United States, North Charleston, South Carolina
Job skills QA/QC
Type Permanent
Job id 163369
Salary Negotiable
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Derek Hinckley
I manage this role
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Position: Visual Inspection Technician I, II, III
Location: Charleston, South Carolina
Shift: 1st Shift | Monday – Friday | 6:00 AM – 2:30 PM
Compensation: $22–$30/hour | Overtime Available
Benefits: Full Benefits Package | Paid Time Off | 401(k) | Relocation Assistance
Job Summary
The Visual Inspection Technician plays a critical role in ensuring the quality and integrity of sterile injectable products intended for commercial distribution and clinical trials. Operating in a fast-paced, regulated environment, this position is responsible for performing detailed visual inspections in compliance with current Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs), and batch records. The role requires precision, consistency, and adherence to safety protocols, including proper use of personal protective equipment (PPE).
Key Responsibilities
Perform visual inspections of sterile liquid products to identify defects such as particulates, air bubbles, or improper sealing.
Follow all applicable SOPs and cGMP guidelines to ensure product quality and regulatory compliance.
Accurately document inspection results and activities in real time using controlled documentation.
Conduct component counting and perform basic mathematical calculations.
Clean and maintain inspection rooms, tools, and equipment.
Ensure inspected products meet appearance and quality specifications before packaging.
Package bulk vials for shipment to other facilities.
Operate material handling equipment as needed.
Complete all required training in a timely manner.
Perform other duties as assigned.
Qualifications
High school diploma or GED required; Associate degree preferred.
Minimum 1 year of GMP experience required; 1–2 years of relevant industry experience preferred.
Experience in pharmaceutical, medical device, biotech, life sciences, food services, or CDMO environments is a plus.
Knowledge, Skills, and Abilities
Must have correctable 20/20 near vision in both eyes (tested annually).
Ability to distinguish colors and detect visual anomalies.
Strong attention to detail and ability to perform repetitive tasks with accuracy.
Proficient in basic math and documentation practices.
Ability to read and follow detailed written instructions.
Effective verbal and written communication skills.
Familiarity with cGMP practices and procedures preferred.
Basic computer literacy required.
Physical Demands & Work Environment
Regularly required to stand, walk, sit, reach, and use hands for extended periods.
Must be able to lift and move up to 50 pounds with assistance.
Frequent exposure to moving mechanical parts, airborne particles, and chemicals.
May occasionally work in humid or wet conditions and around electrical equipment.
Must wear appropriate PPE, including lab coats, gloves, safety eyewear, and respirators as needed.
Work environment noise level is typically moderate.
TRS Staffing Solutions are an equal opportunities employer, and we welcome you to provide OFCCP data voluntarily here (https://fluor.surveymonkey.com/r/NQ9FX79)
We are an equal opportunity employer. All qualified individuals will receive consideration for employment without regard to race; color; age; sex; sexual orientation; gender identity; religion; national origin; disability; veteran status; genetic information; or any other criteria protected by governing law.