Pharmaceutical Manufacturing Technician - 3rd Shift

Fluor Corp; North Charleston (SC); On-site; USD 33,000 - 52,000; Full time

Benefits offered by this job

Full Benefits Package

Paid Time Off

401(k)

Relocation Assistance

Job summary

Fluor Corp is seeking Manufacturing Technicians I–III for its Charleston, SC site to support the production of pharmaceutical drug products, including parenteral or solid dosage forms. You will operate equipment, follow cGMPs, and document activities in real time to ensure quality and compliance.

This hands-on role requires teamwork, precision, and adherence to safety. A high school diploma and at least 1 year of GMP experience are expected; associate or bachelor’s degree is a plus.

Qualifications

• High school diploma or GED required; Associate’s or Bachelor’s degree preferred.
• Minimum 1 year of experience in a GMP‑regulated environment (pharmaceutical, biotech, medical device, food services, or life sciences).

Responsibilities

• Operate manufacturing and material handling equipment in accordance with SOPs and cGMP standards.
• Accurately document all activities in real‑time using controlled documentation systems.
• Perform in‑process testing, weight checks, and basic calculations.
• Clean and sanitize rooms, tools, and equipment to maintain a sterile environment.
• Support cross‑functional manufacturing areas as needed.
• Follow all safety protocols, including proper PPE gowning procedures.
• Complete all required training in a timely and compliant manner.
• Perform other duties as assigned.

Skills

Verbal communication

Attention to detail

Troubleshooting

Basic math

Computer literacy

cGMP basics

Education

High school diploma

Associate or Bachelor degree preferred

Job description

Job details

Posted 31 August 2026

Start date 01 October 2026

Location North Charleston

Job type Permanent

Discipline Pharmaceutical

Reference 169577

Job Function Technician

Position: Manufacturing Technician I, II, III

Location: Charleston, South Carolina

Shift: 3rd Shift | Sunday – Thursday | 11:00 PM – 7:30 AM

Compensation: $24–$38/hour + Shift Differential | Overtime Available

Benefits: Full Benefits Package | Paid Time Off | 401(k) | Relocation Assistance

Position Overview

We are seeking motivated and detail-oriented Manufacturing Technicians (Levels I–III) to join our growing team in Charleston, SC. In this role, you will support the production of pharmaceutical drug products (parenteral or solid dosage) for both commercial distribution and clinical trials. You will operate manufacturing equipment, follow strict regulatory guidelines, and ensure compliance with current Good Manufacturing Practices (cGMPs).

This is a hands‑on role in a fast‑paced, highly regulated environment that requires precision, teamwork, and a commitment to quality.

Key Responsibilities

• Operate manufacturing and material handling equipment in accordance with SOPs and cGMP standards.

• Accurately document all activities in real‑time using controlled documentation systems.

• Perform in‑process testing, weight checks, and basic calculations.

• Clean and sanitize rooms, tools, and equipment to maintain a sterile environment.

• Support cross‑functional manufacturing areas as needed.

• Follow all safety protocols, including proper PPE gowning procedures.

• Complete all required training in a timely and compliant manner.

• Perform other duties as assigned.

Sterile Liquid Manufacturing Technologies

• Equipment and component preparation and sterilization

• Compounding of sterile solutions

• Aseptic filling operations

• Capping and sealing processes

Qualifications

• High school diploma or GED required; Associate’s or Bachelor’s degree preferred.

• Minimum 1 year of experience in a GMP‑regulated environment (pharmaceutical, biotech, medical device, food services, or life sciences).

Skills & Competencies

• Strong verbal and written communication skills.

• High attention to detail and organizational ability.

• Basic troubleshooting and problem‑solving skills.

• Ability to perform basic math and follow detailed written instructions.

• Comfortable working with computers and digital documentation systems.

• Familiarity with cGMP practices preferred.

Physical Requirements & Work Environment

• Regularly required to stand, walk, reach, and use hands for extended periods.

• Must be able to lift/move up to 25 lbs frequently and up to 50 lbs occasionally (with assistance).

• Exposure to moving mechanical parts, airborne particles, and chemicals.

• Use of PPE including safety glasses, gloves, respirators, and full‑body coverings is mandatory.

• May require working at heights or operating industrial vehicles.

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.